Giuseppe Attardi | Academic Influence

Giuseppe Attardi's AcademicInfluence.com Rankings

Giuseppe Attardi

Biology

#2203

World Rank

#3529

Historical Rank

#994

USA Rank

Genetics

#261

World Rank

#311

Historical Rank

#126

USA Rank

biology Degrees

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Biology

Giuseppe Attardi's Degrees

PhD Genetics University of Pavia

Why Is Giuseppe Attardi Influential?

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According to Wikipedia, Giuseppe Attardi was an American molecular biologist of Italian origin, a professor at the California Institute of Technology in Pasadena. He made pioneering studies on the human mitochondrial structure and function.

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Giuseppe Attardi's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

tRNA punctuation model of RNA processing in human mitochondria (1981) (2147)
Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation. (1989) (1655)
Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. (1999) (721)
Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase (1985) (471)
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts. (1992) (460)
Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology* (2006) (403)
Isolation of human cell lines lacking mitochondrial DNA. (1996) (352)
Distinctive features of the 5′-terminal sequences of the human mitochondrial mRNAs (1981) (324)
URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. (1986) (323)
Animal mitochondrial DNA: an extreme example of genetic economy. (1985) (322)
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria. (1991) (297)
Giant-size rapidly labeled nuclear ribonucleic acid and cytoplasmic messenger ribonucleic acid in immature duck erythrocytes. (1966) (284)
The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units (1983) (282)
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. (1992) (282)
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination (1995) (281)
Termination of transcription in human mitochondria: Identification and purification of a DNA binding protein factor that promotes termination (1989) (279)
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication (2001) (271)
Identification of initiation sites for heavy-strand and light-strand transcription in human mitochondrial DNA. (1982) (271)
The tRNA genes punctuate the reading of genetic information in human mitochondrial DNA (1980) (268)
Structure and synthesis of ribosomal RNA. (1970) (251)
Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA (1988) (246)
MtDNA mutations in aging and apoptosis. (2003) (240)
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation. (1996) (237)
Low Reserve of Cytochrome c Oxidase Capacity in Vivo in the Respiratory Chain of a Variety of Human Cell Types* (1998) (212)
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation. (2001) (197)
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity. (2000) (196)
The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNASer(UCN) Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression (1998) (195)
Biogenesis of mitochondria. (1970) (193)
The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes* (2000) (193)
Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles (1994) (187)
Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable (1981) (186)
Association of a protein structure of probable membrane derivation with HeLa cell mitochondrial DNA near its origin of replication. (1977) (184)
The mtDNA‐encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme (1998) (181)
In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells. (1997) (179)
Termination Factor-Mediated DNA Loop between Termination and Initiation Sites Drives Mitochondrial rRNA Synthesis (2005) (178)
Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone (1987) (175)
Mitochondrial growth and division during the cell cycle in HeLa cells (1977) (172)
Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes (2003) (171)
The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions (1997) (167)
Respiration and Growth Defects in Transmitochondrial Cell Lines Carrying the 11778 Mutation Associated with Leber's Hereditary Optic Neuropathy* (1996) (157)
Characterization of an RNase P activity from HeLa cell mitochondria. Comparison with the cytosol RNase P activity. (1985) (152)
Use of polarography to detect respiration defects in cell cultures. (1996) (146)
Nucleotide sequence of a region of human mitochondrial DNA containing the precisely identified origin of replication (1979) (141)
Symmetrical in vivo transcription of mitochondrial DNA in HeLa cells. (1971) (139)
The RNase P Associated with HeLa Cell Mitochondria Contains an Essential RNA Component Identical in Sequence to That of the Nuclear RNase P (2001) (136)
Expression of the mitochondrial genome in HeLa cells. I. Properties of the discrete RNA components from the mitochondrial fraction. (1971) (135)
Discovery of a Major D-Loop Replication Origin Reveals Two Modes of Human mtDNA Synthesis (2004) (126)
Impaired ATP Synthase Assembly Associated with a Mutation in the Human ATP Synthase Subunit 6 Gene* (2001) (125)
Membrane-bound ribosomes in HeLa cells. I. Their proportion to total cell ribosomes and their association with messenger RNA. (1969) (123)
Methylation of nucleic acids in HeLa cells. (1965) (122)
Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers. (1994) (122)
In vivo control of respiration by cytochrome c oxidase in human cells. (2000) (120)
Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems. (1995) (116)
Tight Control of Respiration by NADH Dehydrogenase ND5 Subunit Gene Expression in Mouse Mitochondria (2000) (114)
Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant (2006) (113)
Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells. (1993) (112)
Two distinct genes for ADP/ATP translocase are expressed at the mRNA level in adult human liver. (1988) (111)
Lack of Complex I Activity in Human Cells Carrying a Mutation in MtDNA-encoded ND4 Subunit Is Corrected by theSaccharomyces cerevisiae NADH-Quinone Oxidoreductase (NDI1) Gene* (2001) (110)
Identification of a Novel Mitochondrial Complex Containing Mitofusin 2 and Stomatin-like Protein 2* (2007) (108)
Proportion of HeLa cell genome complementary to transfer RNA and 5 s RNA. (1971) (106)
Molecular and biological characterization of messenger RNA. (1961) (105)
Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase (1995) (103)
Expression of the mitochondrial genome in HeLa cells. VI. Size determination of mitochondrial ribosomal RNA by electron microscopy. (1971) (103)
Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR). (1999) (102)
Marked aging‐related decline in efficiency of oxidative phosphorylation in human skin fibroblasts (2003) (101)
Expression of the mitochondrial genome in HeLa cells. II. Evidence for complete transcription of mitochondrial DNA. (1971) (100)
Lack of assembly of mitochondrial DNA‐encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene product. (1993) (99)
Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells* (1996) (99)
Very Rare Complementation between Mitochondria Carrying Different Mitochondrial DNA Mutations Points to Intrinsic Genetic Autonomy of the Organelles in Cultured Human Cells* (2000) (97)
Partial sequence analysis of ribosomal RNA from HeLa cells. I. Oligonucleotide pattern of 28 s and 18 s RNA after pancreatic ribonuclease digestion. (1968) (97)
Partial sequence analysis of ribosomal RNA from HeLa cells. II. Evidence for sequences of non-ribosmal type in 45 and 32 s ribosomal RNA precursors. (1968) (97)
Functional and morphological abnormalities of mitochondria harbouring the tRNALeu(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease (1999) (96)
Production of Messenger RNA and Regulation of Protein Synthesis (1963) (95)
Fractionation of mitochondrial RNA from HeLa cells by high-resolution electrophoresis under strongly denaturing conditions. (1978) (93)
Flux control of cytochrome c oxidase in human skeletal muscle. (2000) (93)
Mapping of nascent light and heavy strand transcripts on the physical map of HeLa cell mitochondrial DNA. (1980) (90)
Molecular characterization of the transcription termination factor from human mitochondria. (1993) (90)
Isolation, subunit composition, and site of synthesis of human cytochrome c oxidase. (1980) (90)
Expression of the mitochondrial genome in HeLa cells. XIV. The relative positions of the 4 S RNA genes and of the ribosomal RNA genes in mitochondrial DNA. (1972) (88)
Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number. (1996) (78)
An electron microscope study of the relative positions of the 4S and ribosomal RNA genes in HeLa cell mitochondrial DNA (1976) (78)
Expression of the mitochondria genome in HeLa cells. IV. Titration of mitochondrial genes for 16 s, 12 s and 4 s RNA. (1971) (78)
Expression of the mitochondrial genome in HeLa cells. 13. Effect of selective inhibition of cytoplasmic or mitochondrial protein synthesis on mitochondrial nucleic acid synthesis. (1972) (74)
[28] Mitochondria-mediated transformation of human ϱ0 cells (1996) (73)
Novel submicroscopic extrachromosomal elements containing amplified genes in human cells (1987) (72)
Highly efficient RNA-synthesizing system that uses isolated human mitochondria: new initiation events and in vivo-like processing patterns (1984) (72)
Markedly different ATP requirements for rRNA synthesis and mtDNA light strand transcription versus mRNA synthesis in isolated human mitochondria. (1987) (70)
Evidence for complete symmetrical transcription in vivo of mitochondrial DNA in HeLa cells. (1975) (69)
Expression of the mitochondrial genome in HeLa cells. IX. Replication of mitochondrial DNA in relationship to cell cycle in HeLa cells. (1972) (69)
ISOLATION OF METAPHASE CHROMOSOMES FROM HELA CELLS (1966) (69)
Analysis of aminoacylation of human mitochondrial tRNAs. (1996) (68)
Organization and expression of the mammalian mitochondrial genome: a lesson in economy☆ (1981) (68)
Relationship between HeLa cell ribosomal RNA and its precursors studied by high resolution RNA-DNA hybridization. (1969) (65)
Differential regulation of expression of the multiple ADP/ATP translocase genes in human cells. (1991) (64)
Studies of fractionated HeLa cell metaphase chromosomes: I. The chromosomal distribution of DNA complementary to 28 s and 18 s ribosomal RNA and to cytoplasmic messenger RNA (1967) (64)
Sequence analysis and precise mapping of the 3' ends of HeLa cell mitochondrial ribosomal RNAs. (1982) (63)
Regulation of mitochondrial gene expression in mammalian cells. (1990) (60)
Stability of cytoplasmic messenger RNA in HeLa cels. (1973) (59)
Uniparental propagation of mitochondrial DNA in mouse-human cell hybrids. (1980) (58)
Distribution of repetitive and nonrepetivite sequence transcripts in HeLa mRNA. (1974) (58)
Oligonucleotide pattern after pancreatic ribonuclease digestion and the 3' and 5' termini of 5S ribonucleic acid from HeLa cells. (1969) (57)
High molecular weight nonribosomal-type nuclear RNA and cytoplasmic messenger RNA in HeLa cells. (1966) (56)
Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria (1983) (53)
Human dihydrofolate reductase gene organization. Extensive conservation of the G + C-rich 5' non-coding sequence and strong intron size divergence from homologous mammalian genes. (1984) (53)
A small polyadenylated RNA (7 S RNA), containing a putative ribosome attachment site, maps near the origin of human mitochondrial DNA replication. (1981) (53)
Mitochondrial Outer Membrane Permeability Change and Hypersensitivity to Digitonin Early in Staurosporine-induced Apoptosis* (2003) (53)
ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. I. SINGLE CELL RESPONSES TO SEVERAL ANTIGENS. (1964) (52)
The mechanism of protein synthesis. (1967) (52)
Expression of the mitochondrial genome in HeLa cells. X. Properties of mitochondrial polysomes. (1972) (52)
Identification and partial characterization of multiple discrete polyadenylic acid containing RNA components coded for by HeLa cell mitochondrial DNA. (1974) (52)
Expression of the mitochondrial genome in HeLa cells. XIX. Occurrence in mitochondria of polyadenylic acid sequences, "free" and covalently linked to mitochondrial DNA-coded RNA. (1974) (51)
Distinctive pattern and translational control of mitochondrial protein synthesis in rat brain synaptic endings. (1991) (51)
The nucleotide sequence of the cDNA coding for the human dihydrofolic acid reductase. (1983) (50)
The sequences of the small ribosomal RNA gene and the phenylalanine tRNA gene are joined end to end in human mitochondrial DNA (1980) (50)
Symposium on the biology of cells modified by viruses or antigens. II. On the analysis of antibody synthesis at the cellular level. (1959) (49)
Failure to detect "cap" structures in mitochondrial DNA-coded poly(A)-containing RNA from HeLa cells. (1978) (49)
In vitro protein synthesis in a mitochondrial fraction from HeLa cells: sensitivity to antibiotic and ethidium bromide. (1970) (49)
EXPRESSION OF THE MITOCHONDRIAL GENOME IN HELA CELLS (1973) (48)
The multiple ADP/ATP translocase genes are differentially expressed during human muscle development. (1992) (48)
Intercalating drugs and low temperatures inhibit synthesis and processing of ribosomal RNA in isolated human mitochondria. (1984) (48)
Recognition of ribosomal RNA sites in DNA. II. The HeLa cell system. (1965) (48)
Studies of fractionated HeLa cell metaphase chromosomes. II. chromosomal distribution of sites for transfer RNA and 5 s RNA. (1971) (47)
Amino acid specificity of the transfer RNA species coded for by HeLa cell mitochondrial DNA. (1976) (47)
Early appearance and long-term persistence of the submicroscopic extrachromosomal elements (amplisomes) containing the amplified DHFR genes in human cell lines. (1990) (47)
Mitochondrial Ribosomes in HeLa Cells (1971) (47)
Nuclear control of cloverleaf structure of human mitochondrial tRNA(Lys). (2004) (47)
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence. (1982) (46)
Decreased Reactive Oxygen Species Production in Cells with Mitochondrial Haplogroups Associated with Longevity (2012) (46)
Recognition of ribosomal RNA sites in DNA. I. Analysis of the E. coli system. (1965) (46)
Fate of mitochondrial DNA in human-mouse somatic cell hybrids (density gradient centrifugation-ethidium bromide-karyotype). (1972) (45)
Myoclonic Epilepsy and Ragged Red Fibers (MERRF) Syndrome: Selective Vulnerability of CNS Neurons Does Not Correlate with the Level of Mitochondrial tRNAlys Mutation in Individual Neuronal Isolates (1997) (44)
In vivo measurements of respiration control by cytochrome c oxidase and in situ analysis of oxidative phosphorylation. (2001) (43)
The mutation rate of the human mtDNA deletion mtDNA4977. (1996) (43)
Pattern of RNA synthesis in duck erythrocytes in relationship to the stage of cell differentiation. (1970) (43)
Reversible tenfod reduction in mitochondrial DNA content of human cells treated with ethidium bromide (1978) (42)
Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA. (1983) (41)
High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells. (1982) (41)
Variable content of double minute chromosomes is not correlated with degree of phenotype instability in methotrexate-resistant human cell lines. (1982) (40)
The elucidation of the human mitochondrial genome: a historical perspective. (1986) (40)
Biogenesis of mitochondrial proteins in HeLa cells. (1979) (40)
A human dihydrofolate reductase pseudogene and its relationship to the multiple forms of specific messenger RNA. (1983) (40)
Expression of the mitochondrial genome in HeLa cells. XI. Isolation and characterization of transcription complexes of mitochondrial DNA. (1972) (39)
Identification of the polypeptides encoded in the unassigned reading frames 2, 4, 4L, and 5 of human mitochondrial DNA. (1986) (39)
Mitochondrial Gene Products (1987) (38)
Discrete human dihydrofolate reductase gene transcripts present in polysomal RNA map with their 5' ends several hundred nucleotides upstream of the main mRNA start site (1985) (38)
Genetic and Functional Analysis of Mitochondrial DNA‐Encoded Complex I Genes (2004) (38)
Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genes. (1997) (36)
Expression of the mitochondrial genome in HeLa cells. XVI. Electrophoretic properties of the products of in vivo and in vitro mitochondrial protein synthesis. (1973) (36)
Role of mitochondrial DNA in human aging. (2002) (36)
Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase. (1986) (35)
A detailed physical map of HeLa cell mitochondria DNA and its alignment with the positions of known genetic markers. (1977) (35)
Cytoplasmically inherited mutations of a human cell line resulting in deficient mitochondrial protein synthesis (1979) (35)
A membrane-associated RNA of cytoplasmic origin in HeLa cells. (1967) (35)
Mitochondrial RNA and protein synthesis in enucleated African green monkey cells. (1978) (34)
Cytoplasmic transfer of chloramphenicol resistance in a human cell line (1978) (34)
Expression of the mitochondrial genome in HeLa cells. V. Transcription of mitochondrial DNA in relationship to the cell cycle. (1971) (33)
Functional Analysis of in Vivo and in Organello Footprinting of HeLa Cell Mitochondrial DNA in Relationship to ATP and Ethidium Bromide Effects on Transcription* (1997) (33)
Human dihydrofolate reductase gene is located in chromosome 5 and is unlinked to the related pseudogenes. (1984) (32)
Metabolic properties of the products of mitochondrial protein synthesis in HeLa cells. (1977) (32)
Identification of discrete electrophoretic components among the products of mitochondrial protein synthesis in HeLa cells. (1975) (32)
Mechanism of mRNA binding to bovine mitochondrial ribosomes. (1989) (32)
A Comprehensive View of Mitochondrial Gene Expression in Human Cells (1982) (32)
ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. II. FURTHER OBSERVATIONS ON THE BEHAVIOR OF SINGLE ANTIBODY-PRODUCING CELLS WITH RESPECT TO THEIR SYNTHETIC CAPACITY AND MORPHOLOGY. (1964) (31)
Sedimentation Properties of RNA Species homologous to Mitochondrial DMA in HeLa Cells (1969) (30)
Synthesis of chicken hemoglobins during erythrocyte differentiation. (1967) (30)
Characterization of an RNA polymerase activity from HeLa cell mitochondria, which initiates transcription at the heavy strand rRNA promoter and the light strand promoter in human mitochondrial DNA. (1985) (30)
Isolation of chloramphenicol-resistant variants from a human cell line (1975) (29)
cDNA-derived amino acid sequence of the NADH-binding 51-kDa subunit of the bovine respiratory NADH dehydrogenase reveals striking similarities to a bacterial NAD(+)-reducing hydrogenase. (1991) (28)
Persistence of thymidine kinase activity in mitochondria of a thymidine kinase-deficient derivative of mouse L cells. (1972) (28)
Characterization of double-stranded RNA from HeLa cell mitochondria. (1975) (28)
A Monomer-to-Trimer Transition of the Human Mitochondrial Transcription Termination Factor (mTERF) Is Associated with a Loss of in Vitro Activity* (2004) (28)
Expression of the mitochondrial genome in HeLa cells. 8. The relative position of ribosomal RNA genes in mitochondrial DNA. (1972) (28)
The putative mRNA for subunit II of human cytochrome c oxidase starts directly at the translation initiator codon (1980) (28)
Rate-limiting Step Preceding Cytochrome c Release in Cells Primed for Fas-mediated Apoptosis Revealed by Analysis of Cellular Mosaicism of Respiratory Changes* (2001) (28)
Inter-mitochondrial complementation of mtDNA mutations and nuclear context (2002) (28)
Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs. (1996) (27)
Identification of discrete polyadenylate-containing RNA components transcribed from HeLa cell mitochondrial DNA. (1974) (27)
Mitochondrial origin of membrane-associated heterogeneous RNA in HeLa cells. (1968) (26)
Identification and mapping of human mitochondrial genes. (1982) (25)
Polarographic assays of respiratory chain complex activity. (2007) (24)
The site of synthesis of the iron-sulfur subunits of the flavoprotein and iron-protein fractions of human NADH dehydrogenase. (1988) (23)
Isolation and characterization of dihydrofolic acid reductase from methotrexate-sensitive and -resistant human cell lines. (1981) (22)
Virus specific protein and a ribo-nucleic acid associated with ribosomes in poliovirus infected HeLa cells. (1962) (22)
In situ photochemical crosslinking of HeLa cell mitochondrial DNA by a psoralen derivative reveals a protected region near the origin of replication. (1981) (21)
[41] Analysis of human mitochondrial RNA (1983) (21)
Antibodies against the COOH-terminal undecapeptide of subunit II, but not those against the NH2-terminal decapeptide, immunoprecipitate the whole human cytochrome c oxidase complex. (1986) (21)
Alignment of the amino terminal amino acid sequence of human cytochrome c oxidase subunits I and II with the sequence of their putative mRNAs. (1981) (21)
MODE OF MITOCHONDRIAL FORMATION IN HELA CELLS (1973) (21)
Heteroplasmic mitochondrial tRNALys mutation and its complementation in MERRF patient‐derived mitochondrial transformants (1995) (20)
Mitochondrial DNA transcription initiation and termination using mitochondrial lysates from cultured human cells. (1996) (19)
Morphological heterogeneity of HeLa cell mitochondria visualized by a modified diaminobenzidine staining technique. (1975) (19)
Specific requirement for ATP at an early step of in vitro transcription of human mitochondrial DNA. (1987) (18)
Antibody Formation by Rabbit Lymph Node Cells (1964) (18)
Fine mapping of the ribosomal RNA genes of HeLa cell mitochondrial DNA. (1980) (18)
Precise localization of the origin of replication in a physical map of HeLa cell mitochondrial DNA and isolation of a small fragment that contains it. (1978) (17)
Quantitative behaviour of cytoplasmic RNA in rat Purkinje cells following prolonged physiological stimulation. (1957) (17)
Electron microscopic visualization of mitochondrial RNA-DNA hybrids. (1971) (17)
Aging-related occurrence in Ashkenazi Jews of leukocyte heteroplasmic mtDNA mutation adjacent to replication origin frequently remodeled in Italian centenarians. (2007) (17)
Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies. (1995) (17)
Atypical pattern of utilization of amino acids for mitochondrial protein synthesis in HeLa cells. (1973) (17)
Transcription of Mitochondrial DNA in HeLa Cells (1970) (16)
Mitochondrial protein synthesis in HeLa cells. (1973) (15)
Isolation and assay of mitochondrial transcription termination factor from human cells. (1996) (15)
Mitochondrial biogenesis and genetics (1995) (15)
Demonstration in vivo and in vitro of Peristaltic Contractions in the Portal Vein of Adult Mammals (Rodents) (1955) (14)
ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. V. CELLULAR HETEROGENEITY IN THE PRODUCTION OF ANTIBODY TO T5. (1964) (14)
Brief Communication: Role of Nuclear Background and in vivo Environment in Variable Segregation Behavior of the Aging-Dependent T414G Mutation at Critical Control Site for Human Fibroblast mtDNA Replication (1999) (13)
Electrofocusing analysis of HeLa cell metaphase chromosomes. (1972) (13)
ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. IV. THE DETAILED METHODS FOR MEASURING ANTIBODY SYNTHESIS BY INDIVIDUAL CELLS, THE KINETICS OF ANTIBODY FORMATION BY RABBITS AND THE PROPERTIES OF CELL SUSPENSIONS. (1964) (13)
Analysis of human mitochondrial RNA. (1983) (12)
Behavior in Vitro of Normal and Neoplastic Melanocytes of the Human Choroid (1959) (12)
Biochemical and electron microscopic characterization of DNA-RNA complexes from HeLa cell mitochondria. (1978) (11)
Selective in vivo damage by "visible" light of BrdU-containing mitochondrial DNA in a thymidine kinase-deficient mouse cell line with persistent mitochondrial enzyme activity. (1975) (10)
A comparison of the primary structures of 28S and 18S ribonucleic acid from HeLa cells and different human tissues. (1971) (10)
Detection and quantification of point mutations in mitochondrial DNA by PCR. (1996) (10)
The excised leader of human cytochrome c oxidase subunit I mRNA which contains the origin of mitochondrial DNA light-strand synthesis accumulates in mitochondria and is polyadenylated. (1987) (9)
Assignment of human dihydrofolate reductase gene to band q23 of chromosome 5 and of related pseudogene ΨHD1 to chromosome 3 (1985) (9)
Expression of the mitochondrial genome in HeLa cells. XXI. Mitochondrial protein synthesis during the cell cycle. (1974) (9)
ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS.III. THE CONTROLS FOR MICRODROP AND MICROPIPET EXPERIMENTS. (1964) (9)
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments. (1984) (9)
THE ORGANIZATION OF THE GENES IN THE HUMAN MITOCHONDRIAL GENOME AND THEIR MODE OF TRANSCRIPTION (1979) (8)
ANALYSIS OF RNA SYNTHESIZED BY AN ISOLATED RAT BRAIN SYNAPTOSOMAL FRACTION (1976) (8)
Screening for aging-dependent point mutations in mtDNA. (2002) (8)
Nucleotide sequence of a fragment of HeLa-cell mitochondrial DNA containing the precisely localized origin of replication. (1979) (7)
Expression of the mitochondrial genome in HeLa cells. XII. Relationship between mitochondrial fast-sedimenting RNA components and ribosomal and 4 s RNA. (1972) (6)
Transcription system using a HeLa cell mitochondrial lysate. (1995) (5)
Expression of the mitochondrial genome in HeLa cells. XVII. Heterogeneity of isolated HeLa cell mitochondria as assayed for their enzymatic and in vivo biosynthetic activities. (1973) (5)
Analysis of sequence homology between human and mouse mitochondrial DNA. (1980) (5)
Photosensitivity and heat resistance conferred by BrdU incorporation upon a thymidine kinase-deficient mouse cell line with persistent mitochondrial enzyme activity. (1975) (5)
Identification ofinitiation sites forheavy-strand andlight-strand transcription inhumanmitochondrial DNA (1982) (5)
Spontaneous peristaltic activity of veins of chick embryos and newly hatched chickens explantedin vitro (1955) (5)
Heterogeneous Efficiencies of mRNA Translation in Human Mitochondria (1987) (4)
MOLECULAR APPROACHES TO THE DISSECTION OF THE MITOCHONDRIAL GENOME IN HELA CELLS (1974) (4)
Mitochondrial ribssome in HeLa cells. (1971) (4)
In vivo incorporation of different amino acids into electrophoretically characteristic polypeptides synthesized by HeLa cell mitochondria. (1977) (4)
Chapter 20 Recent advances on mitochondrial biogenesis (1992) (3)
Molecular and genetic approaches to the analysis of the informational content of the mitochondrial genome in mammalian cells (1977) (3)
Size distribution of poly(A)-containing messenger RNA from free polysomes of HeLa cells. (1977) (2)
Mitochondrial protein synthesis in rat brain synaptosomes. (1996) (2)
Role of Mitochondrial DNA in Aging Processes (2001) (2)
Functions of the Proteins Encoded in Human Mitochondrial DNA (1987) (2)
In vivo footprinting of human mitochondrial DNA in cultured cell systems. (1996) (2)
Use of a DNA probe for mapping by electron microscopy the ribosomal sequences in ribosomal RNA precursors from duck cells. (1974) (2)
[Cultivation in vitro of fixed corneal cells of chick embryo]. (1954) (1)
Spontaneous peristaltic activity in arteries and veins of adult goldfinches and albino mice cultivatedin vitro (1955) (1)
Mitochondrial and nuclear gene interaction in HeLa cells. (1977) (1)
[Effect of enzymatic induction on the rate of synthesis of a specific messenger RNA in E. coli]. (1962) (0)
[Regulation of the DNA-RNA transcription messenger intervening in the biosynthesis of bacterial enzymes and the expression of phage viral functions]. (1963) (0)
MERRF SYNDROME: MITOCHONDRIAL DNA MUTATION IN NEURONAL ISOLATES (1996) (0)
An electron microscope study of the relative positions of the 4S and ribosomal RNA genes in HeLa cells mitochondrial DNA. (1976) (0)
Abstracts of papers presented at the Meeting on Mitochondrial Genes, May 13-May 17, 1981 (1981) (0)
Cytoplasmically determined human cell mutants defective in mitochondrial ribosome assembly (2004) (0)
Identification and mapping of human mitochondrial genes. (1982) (0)
[Peculiar morphological aspect of the elements in culture of chick embryo myocardium]. (1951) (0)
[New and quick methods for determination of cellular sizes]. (1953) (0)
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria (1991) (0)
The effects of sodium paraminosalicylate on the growth of pure cultures of embryo chick myoblasts (1952) (0)
[New rapid method of cytometry]. (1951) (0)
A MEMBRANE-ASSOCIATED RNA OF CYTOPLASMIC ORIGIN (2016) (0)
RECOGNITION OF RIBOSOAMAL RNA SITES IN DNA , II . THE HELA CELL SYSTEM 1 * BY (0)
Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
Mitochondrial DNA: The Second Genetic System (1990) (0)
RNase on the hybridized RNA , in COMPARATIVE OVER-ALL LEVEL OF agreement with the fact that the ratio 2 ' HYBRIDIZATION OF HELA 28 S to 3 ' cytidylic acid was considerably RNA WITH VARIOUS (0)
Nucleic Acids Research Alignment of the amino terninal amino acid sequence of human cytochrome c oxidase subunits I and II with the sequence of their putative mRNAs (0)
STIMULATION OF THE RATE OF SYNTHESIS OF SPECIFIC MESSENGER RNA AFTER ENZYME INDUCTION IN E. COLI (1963) (0)
I S O L a T I O N of M E T a P H a S E Cultivation of Cells (0)
The excised leader of human cytochrome c oxidase subunit I mRNA which contains the origin of mitochondrial DNA light-strand synthesis accumulates in mitochondria and is polyadenylated (1987) (0)
[Morphological modification of nerve cells of the albino rat fed with a hyperprotein and hyperpurine diet]. (1952) (0)
[In vitro culture of malignant melanoma of the choroid]. (1953) (0)
1964 Gordon Research Conference on Nucleic Acids (2008) (0)
An ultraviolet microspectrophotometric study of the purkinje cells of the adult albino rat (1953) (0)
Table of Contents (1993) (0)
TheMutation RateoftheHumanmtDNADeletion mtDNA4977 (1996) (0)
[Active pulsation of the portal vein in rodents investigated in vivo]. (1955) (0)
cDNA-derived aminoacidsequence oftheNADH-binding 51-kDa subunit ofthebovine respiratory NADH dehydrogenase reveals striking similarities toabacterial NAD+-reducing hydrogenase (Akaligenes eutrophus/mRNA levels indssues/human genonic sequences) (1991) (0)
Subject Index Vol. 32, 1982 (1982) (0)
Stability of Cytoplasmic Messenger RNA ii (actinomycin D/benzoylated-DEAE-cellulose/poly(T)-cell (2016) (0)
ON THE BIOLOGY OF CELLS MODIFIED BY VIRUSES OR ANTIGENS (0)
Fate of Mitochondrial DNA in Human-M( (density gradient centrifugation/ethidium bromide/kary (2016) (0)
[Simple and rapid method for measuring the mean area of microscopic objects with circular section]. (1951) (0)
Variable content of double minute chromosomes is not correlated with degree of phenotype instability in methotrexate-resistant human cell lines (1982) (0)
Symmetrical InVivoTranscription ofMitochondrial DNA inHeLaCells (1971) (0)
[Effect of prolonged thymic diet on thyroid gland; studies on the adult albino rat]. (1953) (0)
Contents, Vol. 32, 1982 (1982) (0)

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