Samuel A. Latt
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Samuel A. Lattbiology Degrees
Biology
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#12125
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Molecular Biology
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Biochemistry
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#1458
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Biology
Samuel A. Latt's Degrees
- PhD Biochemistry University of California, Berkeley
- Bachelors Chemistry Stanford University
Why Is Samuel A. Latt Influential?
(Suggest an Edit or Addition)Samuel A. Latt's Published Works
Number of citations in a given year to any of this author's works
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
- Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. (1973) (811)
- Automatic measurement of sister chromatid exchange frequency. (1977) (779)
- Transposition and amplification of oncogene-related sequences in human neuroblastomas (1983) (663)
- Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. (1989) (557)
- Sister chromatid exchanges, indices of human chromosome damage and repair: detection by fluorescence and induction by mitomycin C. (1974) (482)
- Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. (1985) (434)
- Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. (1985) (384)
- Spectral studies on 33258 Hoechst and related bisbenzimidazole dyes useful for fluorescent detection of deoxyribonucleic acid synthesis. (1976) (344)
- Coamplification and coexpression of human tissue-type plasminogen activator and murine dihydrofolate reductase sequences in Chinese hamster ovary cells (1985) (281)
- Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. (1975) (262)
- Stimulated human phagocytes produce cytogenetic changes in cultured mammalian cells. (1983) (256)
- A simplified technique for in vivo analysis of sister-chromatid exchanges using 5-bromodeoxyuridine tablets. (1977) (196)
- Localization of Sister Chromatid Exchanges in Human Chromosomes (1974) (193)
- Sister-chromatid exchanges. (1979) (181)
- Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance. (1987) (175)
- Sister chromatid exchange formation. (1981) (169)
- Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. (1982) (168)
- Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. (1986) (153)
- Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence. (1975) (153)
- Analysis of sister chromatid exchange formation in vivo in mouse spermatogonia as a new test system for environmental mutagens (1976) (149)
- Optical studies of the interaction of 33258 Hoechst with DNA, chromatin, and metaphase chromosomes (1975) (146)
- Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. (1989) (145)
- The amyloid beta protein gene is not duplicated in brains from patients with Alzheimer's disease. (1987) (138)
- Induction of sister chromatid exchanges by BUdR is largely independent of the BUdR content of DNA (1980) (135)
- Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. (1976) (123)
- Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism. (1986) (118)
- Bromodeoxyuridine tablet methodology for in vivo (1978) (109)
- Sister chromatid exchange analysis. (1980) (108)
- Evolution of chromosomal regions containing transfected and amplified dihydrofolate reductase sequences (1983) (99)
- Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus. (1984) (99)
- Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment. (2005) (98)
- Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes. (1983) (98)
- Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females. (1986) (93)
- A novel alteration in the structure of an activated c-myc gene in a variant t(2;8) burkitt lymphoma (1984) (92)
- Sister-chromatid exchanges: a report of the GENE-TOX program. (1981) (87)
- Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus. (1985) (85)
- Flow cytometric analysis of bromodeoxyuridine-substituted cells stained with 33258 Hoechst. (1977) (85)
- Fluorescence analysis of late DNA replication in human metaphase chromosomes (1975) (78)
- Microfluorometric detection of asymmetry in the centromeric region of mouse chromosomes. (1974) (77)
- Characterization of sister chromatid exchange induction by 8-methoxypsoralen plus near UV light. (1978) (75)
- Leukemia relapse in donor cells after allogeneic bone-marrow transplantation. (1981) (73)
- Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 Hoechst. (1974) (71)
- MICROFLUOROMETRIC ANALYSIS OF DEOXYRIBONUCLEIC ACID REPLICATION KINETICS AND SISTER CHROMATID EXCHANGES IN HUMAN CHROMOSOMES (1974) (66)
- Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines. (1985) (66)
- Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female. (1986) (65)
- In vitro and in vivo analysis of sister chromatid exchange. (1978) (63)
- Energy transfer and binding competition between dyes used to enhance staining differentiation in metaphase chromosomes (2004) (63)
- 5-Bromodeoxyuridine-dependent increase in sister chromatid exchange formation in Bloom's syndrome is associated with reduction in topoisomerase II activity. (1987) (61)
- Optical studies of metaphase chromosome organization. (1976) (60)
- Sister chromatid exchanges. (1980) (59)
- Analysis of peripheral maternal blood samples for the presence of placenta‐derived cells using Y‐specific probes and McAb H315 (1988) (56)
- Fluorescent probes of chromosome structure and replication. (1977) (53)
- Amplification and rearrangement of DNA sequences from the chromosomal region 2p24 in human neuroblastomas. (1986) (53)
- Fluorometric detection of deoxyribonucleic acid synthesis; possibilities for interfacing bromodeoxyuridine dye techniques with flow fluorometry. (1977) (52)
- Microfluorometric analysis of DNA replication in human X chromosomes. (1974) (51)
- The effect of a tumor promoter, 12-O-tetradecanoyl-phorbol-13-acetate (TPA), on sister-chromatid exchange formation in cultured Chinese hamster cells (1979) (51)
- 33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cells (1976) (49)
- BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes (1976) (47)
- Isolation of mouse x-chromosome specific DNA from an x-enriched lambda phage library derived from flow sorted chromosomes. (2005) (47)
- Fluorescence decay analysis in solution and in a microscope of DNA and chromosomes stained with quinacrine. (1979) (47)
- In vivo BrdU-33258 Hoechst analysis of DNA replication kinetics and sister chromatid exchange formation in mouse somatic and meiotic cells (1976) (44)
- Estimation of accessibility of DNA in chromatin from fluorescence measurements of electronic excitation energy transfer (1975) (44)
- Development and use of metaphase chromosome flow-sorting methodology to obtain recombinant phage libraries enriched for parts of the human X chromosome. (1984) (43)
- Flow sorting of the mouse Cattanach X chromosome, T (X; 7) 1 Ct, in an active or inactive state. (1981) (40)
- Pairs of fluorescent dyes as probes of DNA and chromosomes. (1979) (39)
- The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10 (1987) (39)
- Interactions between pairs of DNA-binding dyes: results and implications of chromosome analysis. (1980) (39)
- DETECTION OF DNA SYNTHESIS IN INTERPHASE NUCLEI BY FLUORESCENCE MICROSCOPY (1974) (39)
- Chromosome instability associated with human alphoid DNA transfected into the Chinese hamster genome (1988) (37)
- Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis. (1986) (33)
- Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci. (1985) (33)
- Identification and isolation of transcribed human X chromosome DNA sequences. (1983) (33)
- Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis. (1985) (32)
- Relationship between DNA adduct formation and sister chromatid exchange induction by [3H]8-methoxypsoralen in Chinese hamster ovary cells. (1980) (32)
- Optical studies of complexes of quinacrine with DNA and chromatin: implications for the fluorescence of cytological chromosome preparations (2004) (31)
- Molecular and cytologic analysis of DNA amplification in retinoblastoma. (1985) (29)
- Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP. (1989) (29)
- Energy transfer-enhanced chromosome banding. An overview☆ (1980) (27)
- Construction and use of a dominant, selectable marker: a Harvey sarcoma virus-dihydrofolate reductase chimera. (1983) (26)
- Comparison of benzo(a)pyrene metabolism and sister chromatid exchange induction in mice (1980) (25)
- Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia. (1982) (25)
- Accurate and superaccurate gene mapping. (1985) (25)
- Fluorescence analysis of late DNA replication in mouse metaphase chromosomes using BUdR and 33258 Hoechst. (1976) (25)
- Mapping by chromosome sorting of several gene probes, including c-myc, to the derivative chromosomes of a 3;8 translocation associated with familial renal cancer. (1986) (24)
- In vivo induction of sister-chromatid exchanges in liver and marrow cells by drugs requiring metabolic activation. (1979) (21)
- Cloning and analysis of reverse transcript P160 genomes of Abelson murine leukemia virus (1983) (21)
- Amplification of IMR-32 clones 8, G21, and N-myc in human neuroblastoma xenografts. (1987) (20)
- EFFECT OF PHOTOTHERAPY ON SISTER CHROMATID EXCHANGE IN PREMATURE INFANTS (1978) (19)
- Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature. (1986) (19)
- Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma. (1986) (19)
- 33258 Hoechst enhances the selectivity of the bromodeoxyuridine--light method of isolating conditional lethal mutants. (1977) (19)
- Rapid cloning of multiple amplified nucleotide sequences from human neuroblastoma cell lines by phenol emulsion competitive DNA reassociation. (1987) (18)
- Construction, analysis, and application to 46,XY gonadal dysgenesis of a recombinant phage DNA library from flow-sorted human Y chromosomes. (1986) (17)
- New fluorochromes, compatible with high wavelength excitation, for flow cytometric analysis of cellular nucleic acids. (1984) (17)
- Detection, significance, and mechanism of sister chromatid exchange formation: past experiments, current concepts, future challenges. (1984) (17)
- Differences in murine procarcinogen activation enzymes are not accompanied by parallel differences in procarcinogen-induced sister-chromatid exchange. (1982) (17)
- Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes. (1987) (17)
- Automatic detection and localization of sister chromatid exchanges. (1976) (16)
- Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18. (1987) (16)
- Disparate effects of 5-bromodeoxyuridine on sister-chromatid exchanges and chromosomal aberrations in Bloom syndrome fibroblasts. (1988) (16)
- Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism (1987) (15)
- Parallel induction of sister chromatid exchanges and infectious virus from SV40-transformed cells by alkylating agents (1978) (15)
- Identification of human and mouse chromosomes in human-mouse hybrids by centromere fluorescence. (1974) (14)
- Sister chromatid exchange induction resulting from systemic, topical, and systemic-topical presentations of carcinogens. (1979) (13)
- Use of Y chromosome specific probes to detect low level sex chromosome mosaicism (1986) (13)
- Staining of human metaphase chromosomes with fluorescent conjugates of polylysine. (1973) (12)
- Isolation of guinea pig macrophages bearing surface C4 by fluorescence-activated cell sorting: correlation between surface C4 antigen and C4 protein secretion. (1983) (12)
- Search for DNA interchange corresponding to sister chromatid exchanges in Chinese hamster ovary cells. (1978) (11)
- Comparison of the subunit organization of early and late replicating chromatin. (1977) (11)
- Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome. (1984) (11)
- Further linkage studies between retinoschisis and cloned dna sequences from the distal xp (1985) (9)
- Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome. (1978) (8)
- Amplified inverted duplications within and adjacent to heterologous selectable DNA. (1989) (8)
- Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5). (1985) (8)
- Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p (1987) (8)
- Applications of fluorescence spectroscopy to molecular cytogenetics (1985) (6)
- Genetic analysis of Duchenne dystrophy. (1985) (6)
- Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center (2004) (6)
- Use of fluorescent dyes to study chromosome structure and replication (1977) (6)
- The co-induction of sister chromatid exchanges and virus synthesis in mammalian cells. (1980) (6)
- Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines. (1986) (5)
- Analysis of sister chromatid exchange and chromosome replication kinetics using BrdU-dye techniques (1978) (5)
- Chapter 3. Prenatal Cytogenetic Diagnosis (1982) (4)
- IMPROVED FLUORESCENT STAINING OF INTERPHASE NUCLEI FOR PRENATAL DIAGNOSIS (1979) (3)
- 1022 PHOTOTHERAPY DOES NOT INCREASE THE SISTER CHROMATID EXCHANGE FREQUENCY IN PREMATURE INFANTS (1978) (3)
- Repeated DNA sequences in the distal long arm of the human X chromosome (1986) (3)
- 15 – Metaphase Chromosome Flow Sorting and Cloning; Rationale, Approaches and Applications (1989) (3)
- Isolation by fluorescence activated cell sorting (FACS) of macrophages bearing C4 on their surface membrane (1982) (3)
- Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes (1988) (3)
- Coamplification andCoexpression ofHumanTissue-Type Plasminogen Activator andMurine Dihydrofolate Reductase Sequences inChinese Hamster OvaryCells (1985) (3)
- The effect of a tumor promotor, 12-O-tetradecanoyl-phorbol-13-acetate (TPA), on sister-chromatid exchange formation in cultured Chinese hamster cells. (1979) (2)
- The human T cell antigen Leu-2 (T8) is encoded on chromosome 2 (2004) (2)
- Cytological, flow cytometric, and molecular analysis of the rapid evolution of mammalian chromosomes containing highly amplified DNA sequences (2004) (2)
- An in vivo BrdU technique for analyzing the induction by mutagens of sister chromatid exchanges in mouse spermatogonia (1976) (1)
- Prenatal cytogenetic diagnosis. (1982) (1)
- Construction of an x-enriched lambda phage library from sorted mouse chromosomes. Abstr. (1981) (1)
- DNA-based detection of chromosome deletion and amplification: diagnostic and mechanistic significance. (1986) (1)
- Analysis of human chromosome structure, replication of repair using BrdU-33258 Hoechst techniques. (1976) (1)
- A high buoyant density fraction in mammalian DNA. Characterization and impact on the detection of heteroduplex DNA. (1981) (1)
- Molecular genetic approaches to human diseases involving mental retardation. (1984) (1)
- INVESTIGATIVE APPROACHES FOR THE ANALYSIS OF DRUG INTERACTIONS AT THE GENETIC LEVEL * (1976) (1)
- Subject Index Vol. 33, 1982 (1982) (0)
- Editorial help (2004) (0)
- RFLPs for β2-microglobulin (1989) (0)
- Contents, Vol. 29, 1981 (1981) (0)
- RFLPs for beta 2-microglobulin. (1989) (0)
- Reply to F. Greenberg and D.H. Ledbetter: “Chromosome abnormalities and Williams syndrome” (1988) (0)
- Prenatal diagnosis: cell biological approaches. (1982) (0)
- Sorting, cloning and analysis of specific human chromosomes (1984) (0)
- MICROFLUOROMETRIC ANALYSIS OF SISTER CHROMATID EXCHANGES, INDICES OF CHROMOSOME FRAGILITY (1974) (0)
- Isolation of fetal DNA from nucleated erythrocytes (0)
- Selection of conditional lethal mutants with a bromodeoxyuridine 33258 Hoechst photosensitization technique (1976) (0)
- Subject Index Vol. 29, 1981 (1981) (0)
- Hoechst / BrdU-dependent fluorescence / metaphase chromosome staining / autoradiography ) (0)
- Subject Index Vol. 20, 1978 (1978) (0)
- Fluorescence-Activated Flow Sorting of Metaphase Chromosomes Isolation of Amplified DNA Sequences from IMR-32 Human Neuroblastoma Cells: Facilitation by (2006) (0)
- Human Genetic Mutant Cell Repository Reports Index (1981) (0)
- Localization ofDNA Sequences inRegionXp21ofthe HumanX Chromosome: SearchforMolecular Markers ClosetotheDuchenneMuscular Dystrophy Locus (1985) (0)
- X-CHROMOSOME REPLICATION IN PARTHFNOGENIC BENIGN OVARIAN TERATOMAS (1978) (0)
- Construction analysis and utilization of recombinant phage libraries enriched for the human x chromosome by fluorescence activated flow sorting (1983) (0)
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