Dirk Bootsma | Academic Influence

Dirk Bootsma's AcademicInfluence.com Rankings

Dirk Bootsma

Biology

#3985

World Rank

#6014

Historical Rank

Genetics

#655

World Rank

#739

Historical Rank

Molecular Biology

#738

World Rank

#755

Historical Rank

biology Degrees

Download Badge

Biology

Dirk Bootsma's Degrees

Bachelors Biology University of Amsterdam
Masters Genetics Leiden University
PhD Genetics Utrecht University

Similar Degrees You Can Earn

Best Online Bachelor's in Biology

Why Is Dirk Bootsma Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Dirk Bootsma was a Dutch geneticist. He was a professor at the Erasmus University Rotterdam between 1969 and 2002. He and his research group discovered the cause of chronic myelogenous leukemia and furthered the understanding of the nucleotide excision repair.

(See a Problem?)

Dirk Bootsma'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

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia (1982) (1354)
Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms (1999) (1327)
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair. (1998) (932)
Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia (1983) (715)
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes (1992) (669)
Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. (1975) (631)
Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous Recombination (1997) (463)
Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification (1996) (409)
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome (1990) (404)
Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23. (1994) (400)
Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia (1987) (395)
Xeroderma pigmentosum: biochemical and genetic characteristics. (1975) (379)
Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence (1997) (356)
STUDIES ON SYNCHRONOUS DIVISION OF TISSUE CULTURE CELLS INITIATED BY EXCESS THYMIDINE. (1964) (336)
Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition (1997) (331)
Genetic heterogeneity of xeroderma pigmentosum demonstrated by somatic cell hybridization. (1972) (299)
Molecular cloning of a human DNA repair gene (1984) (293)
Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10 (1986) (262)
The Cockayne syndrome B protein, involved in transcription‐coupled DNA repair, resides in an RNA polymerase II‐containing complex (1997) (256)
RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6. (1994) (250)
Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6. (1991) (244)
Engagement with transcription (1993) (216)
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients. (1988) (189)
Five complementation groups in xeroderma pigmentosum. (1975) (187)
HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro (1996) (173)
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F. (1993) (167)
Loss of human genetic markers in man--Chinese hamster somatic cell hybrids. (1971) (166)
International system for human gene nomenclature (1979) ISGN (1979). (1979) (161)
A seventh complementation group in excision-deficient xeroderma pigmentosum. (1979) (159)
Is the chromosomal region 9q34 always involved in variants of the Ph1 translocation? (1984) (156)
Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation. (1970) (149)
Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma. (1995) (147)
Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. (1994) (142)
Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity (1997) (140)
Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas. (1994) (135)
Synchronization of mammalian cells in vitro by inhibition of the DNA synthesis. I. Optimal conditions. (1966) (134)
XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes (1996) (126)
Mutational analysis of the human nucleotide excision repair gene ERCC1. (1996) (124)
Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein. (1994) (123)
Induction of sister chromatid exchanges in xeroderma pigmentosum cells after exposure to ultraviolet light. (1977) (117)
Improved identification of chromosomes of leukemic cells in methotrexate-treated cultures. (1979) (116)
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH). (1994) (116)
Molecular cloning and biological characterization of the human excision repair gene ERCC-3 (1990) (111)
Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion. (1982) (111)
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome. (1993) (111)
Molecular cloning of the human DNA excision repair gene ERCC-6 (1990) (110)
Identification and characterization of XPC-binding domain of hHR23B (1997) (108)
UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice. (2002) (106)
The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation. (1981) (106)
c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia (1983) (100)
A ninth complementation group in xeroderma pigmentosum, XP I. (1985) (98)
The cellular retinoic-acid-binding protein is expressed in tissues associated with retinoic-acid-induced malformations. (1990) (97)
Replication pattern of the X chromosomes in three X/autosomal translocations. (1977) (91)
Molecular genetics of eukaryotic DNA excision repair. (1990) (89)
Sequence conservation of the rad21 Schizosaccharomyces pombe DNA double-strand break repair gene in human and mouse. (1996) (87)
Synchronization of mammalian cells in vitro by inhibition of the DNA synthesis. II. Population dynamics. (1966) (83)
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes. (1973) (81)
A third complementation group in xeroderma pigmentosum. (1974) (80)
Abnormal regulation of DNA replication and increased lethality in ataxia telangiectasia cells exposed to carcinogenic agents. (1982) (79)
Cloning, tissue expression, and mapping of a human photolyase homolog with similarity to plant blue-light receptors. (1996) (76)
Repair of x-ray damage in DNA of cultivated cells from patients having xeroderma pigmentosum. (1970) (74)
Xeroderma pigmentosum complementation group H falls into complementation group D. (1991) (73)
Dhr6, a Drosophila homolog of the yeast DNA-repair gene RAD6. (1991) (73)
Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition. (1999) (71)
Nucleotide excision repair syndromes: molecular basis and clinical symptoms. (1995) (71)
Translocation t(6;9) in acute non-lymphocytic leukaemia results in the formation of a DEK-CAN fusion gene. (1992) (69)
Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B. (1993) (68)
Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization. (1974) (66)
Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23. (1996) (65)
The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. (1989) (64)
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids. (1983) (62)
Genomic characterization of the human DNA excision repair gene ERCC-1. (1987) (62)
A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene. (1991) (58)
Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31. (1992) (58)
Clinical characteristics, DNA repair, and complementation groups in xeroderma pigmentosum patients from Egypt. (1980) (58)
Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function (1994) (57)
Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line. (1987) (55)
Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. (1988) (54)
DNA repair. Engagement with transcription. (1993) (49)
Incorporation of isolated chromosomes and induction of hypoxanthine phosphoribosyltransferase in chinese hamster cells (1975) (49)
Conserved pattern of antisense overlapping transcription in the homologous human ERCC-1 and yeast RAD10 DNA repair gene regions (1989) (48)
The genetic basis of xeroderma pigmentosum. (1991) (47)
Preferential expression of cellular retinoic acid binding protein in a subpopulation of neural cells in the developing mouse embryo. (1989) (47)
Genes controlling nucleotide excision repair in eukaryotic cells (1993) (46)
Microinjection of Micrococcus luteus UV-endonuclease restores UV-induced unscheduled DNA synthesis in cells of 9 xeroderma pigmentosum complementation groups. (1985) (46)
Assignment of the AK1:Np:ABO linkage group to human chromosome 9. (1976) (45)
Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations. (1984) (45)
Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1979) (44)
The progression of mammalian cells through the division cycle following ultraviolet irradiation. (1968) (44)
The regulation of cell proliferation and differentiation in intestinal epithelium. II. A quantitative histochemical and autoradiographic study after low doses of x-irradiation. (1969) (43)
Mammalian nucleotide excision repair and syndromes. (1997) (42)
The molecular basis of nucleotide excision repair syndromes. (1994) (42)
Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line (1985) (41)
International System for Human Gene Nomenclature (1979) ISGN (1979). (1980) (39)
A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A. (1976) (38)
Effects of inhibitors on repair of DNA in normal human and xeroderma pigmentosum cells after exposure to x-rays and ultraviolet irradiation. (1973) (38)
Nomenclature of human DNA repair genes. (1994) (36)
X-Linkage of Human α-Galactosidase (1972) (36)
Transfection of the cloned human excision repair gene ERCC-1 to UV-sensitive CHO mutants only corrects the repair defect in complementation group-2 mutants. (1988) (34)
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair (1979) (32)
CHANGES INDUCED IN THE FIRST POST-IRRADIATION GENERATION CYCLE OF HUMAN CELLS STUDIES BY DOUBLE LABELING. (1965) (32)
Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential pyrimidine dimer site. (1989) (31)
Repair of DNA damage after exposure to 4-nitroquinoline-1-oxide in heterokaryons derived from xeroderma pigmentosum cells. (1980) (31)
Human diseases with genetically altered DNA repair processes. (1975) (31)
The genetic defect in DNA repair deficiency syndromes. EACR--Mühlbock Memorial Lecture, 1993. (1993) (31)
Incisions for excision (1994) (29)
Isolation of Chinese hamster ovary cells with reduced unscheduled DNA synthesis after UV irradiation (1982) (28)
Xeroderma pigmentosum complementation group XP-I withdrawn. (1989) (27)
Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome. (1991) (27)
Transfer of the human X chromosome to human-Chinese hamster cell hybrids via isolated HeLa metaphase chromosomes (1976) (25)
Cytogenetics and Cell Genetics (2010) (24)
Expression of human hypoxanthine phosphoribosyl transferase in Chinese hamster cells treated with isolated human chromosomes (1976) (23)
Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells. (1985) (22)
Survival of excess thymidine synchronized cell populations in vitro after x-irradiation in various phases of the cell cycle. (1966) (22)
Xeroderma pigmentosum group A correcting protein from calf thymus. (1992) (21)
Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site. (1992) (21)
Microinjected photoreactivating enzymes from Anacystis and Saccharomyces monomerize dimers in chromatin of human cells. (1985) (20)
Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. (1976) (20)
Transfer of the human genes coding for thymidine kinase and galactokinase to Chinese hamster cells and human-Chinese hamster cell hybrids (1977) (19)
Different rates of restoration of the repair capacity in complementing xeroderma pigmentosum cells after fusion. (1981) (18)
Complementation analysis of xeroderma pigmentosum variants (1981) (18)
Phenotypic correction of the defect in xeroderma pigmentosum cells after fusion with isolated cytoplasts. (1982) (17)
Chromosome and DNA-mediated gene transfer in cultured mammalian cells. (1984) (16)
Synteny of the human loci for fumarate hydratase and udpg pyrophosphorylase with chromosome 1 markers in somatic cell hybrids. (1974) (15)
Unscheduled DNA synthesis in xeroderma pigmentosum cells after microinjection of yeast photoreactivating enzyme. (1986) (15)
RAPID DIAGNOSTIC TEST FOR ATAXIA TELANGIECTASIA (1981) (15)
4th International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, 5, 7, 8, 10, 11, and 12. (1978) (14)
The influence of 5-bromodeoxyuridine on the induction of breaks in the deoxyribonucleic acid of cultivated human cells by x-irradiation and ultraviolet light. (1972) (14)
Mammalian cell culture studies (1973) (14)
α-Galactosidase in man-Chinese hamster somatic cell hybrids (1975) (14)
The genetic defect in the de Sanctis-Cacchione syndrome. (1974) (13)
Constitutional DNA‐level aberrations in chromosome 22 in a patient with multiple meningiomas (1994) (12)
Genetical studied on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids. (1974) (12)
Expression of human hprt gene on the inactive X chromosome after DNA-mediated gene transfer (1982) (12)
Identification of DNA repair genes in the human genome. (1986) (12)
DNA repair in human cells: from genetic complementation to isolation of genes. (1988) (11)
DNA repair: two pieces of the puzzle (1992) (11)
Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase, and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity (1972) (10)
Repair mechanisms in mammalian cells (1974) (10)
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1. (1987) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
Genetic complementation analysis of xeroderma pigmentosum. (1975) (9)
Normal chiasma formation in a male with xeroderma pigmentosum. (2009) (9)
DNA repair. Incisions for excision. (1994) (9)
Cytological mapping of the genes assigned to the human A 1 chromosome by use of radiation-induced chromosome breakage in a human-Chinese hamster hybrid cell line (2004) (9)
Regional mapping of the human immunoglobulin lambda light chain to the Philadelphia chromosome in chronic myeloid leukaemia. (1984) (8)
SYNTHESIS OF RIBONUCLEIC ACID IN REGENERATING RAT LIVER AFTER PARTIAL HEPATECTOMY. (1965) (8)
The Role of the Philadelphia Translocation in Chronic Myelocytic Leukemia (1987) (8)
X Linkage of Human Galactosidase (1972) (8)
Two new linkage groups in man, both carrying different loci for lactate dehydrogenase and glutamic-pyruvic transaminase. (1972) (7)
Abnormal levels of UV-induced unscheduled DNA synthesis in ataxia telangiectasia cells after exposure to ionizing radiation. (1982) (7)
The "Dutch DNA Repair Group", in retrospect. (2001) (7)
Interaction of human and chick DNA repair functions in UV-irradiated xeroderma pigmentosum-chick erythrocyte heterokaryons. (1982) (7)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
Assignment of structural β-galactosidase loci to human chromosomes 3 and 22 (1979) (6)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
MammalianCry 1 andCry 2 areessential formaintenance of circadian rhythms (1999) (5)
MITOTIC DELAY OF HUMAN CELLS IN TISSUE CULTURE IRRADIATED AT DIFFERENT PHASES OF THE GENERATION CYCLE. (1968) (5)
DNA repair defects in genetic diseases in man. (1979) (5)
Abstract of papers presented at the second international workshop, May 2–6, 1976, Noordwijkerhout (The Netherlands) (1977) (5)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
Defective DNA Repair and Cancer (1977) (4)
Alcohol Withdrawal: Possible Risk of Latent Scurvy Appearing as Tiredness: A STROBE-Compliant Study (1983) (4)
Molecular Genetic Dissection of Mammalian Excision Repair (1989) (4)
Claim that two human linkage groups carry different loci for GPT and LDH withdrawn (1974) (4)
Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. (1975) (4)
Cloning of a putative meningioma tumor suppressor gene (1994) (4)
Molecular basis of DNA repair mechanisms and syndromes. (1998) (4)
Third International Congress of Histochemistry and Cytochemistry (1968) (4)
Excision repair in human cells (1975) (3)
Inhibition of DNA synthesis in ataxia telangiectasia fibroblasts after exposure to DNA-damaging agents (1982) (3)
Genetic complementation analysis of ataxia telangiectasia by somatic cell fusion. (1982) (3)
Report of the Committee on the Genetic Constitution of Chromosomes 2, 3, 4, and 5. (1984) (3)
Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. (1976) (3)
Late-replicating ring X-chromosomes identified by r-banding after BrdU pulse (1976) (3)
Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. (1975) (2)
[The dual function of the proliferating cell nuclear antigen (PCNA) in the response of human cells to UV damages]. (1996) (2)
Molecular Cloning of the Human DNA Excision Repair (2)
Proceedings: Report of the Committee on the Genetic Constitution of Autosomes other than Chromosome 1. (1974) (2)
Molecular cloning of part of the human excision repair gene ercc 3 (1988) (2)
Repair DNA synthesis in heterokaryons during reactivation of chick erythrocytes fused with human diploid fibroblasts or HeLa cells. (1982) (2)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. (1975) (1)
Human Genetic Mutant Cell Repository Index / Book Review Index (1974) (1)
Workshop on mapping by somatic cell hybridization. (1982) (1)
Complement analysis of xeroderma pigmentosum variants. (1981) (1)
Localization of Genes Involved in DNA Repair on Human Chromosomes by Using Cell Fusion (1983) (1)
Specific breakpoint analysis: Potentials for detection of minimal residual disease (1986) (1)
Abstract of the 16th annual meeting of the European environmental mutagen society (EEMS) 25–30 August 1986, Brussels (Belgium)Biological and biochemical consequences of the human ERCC1 repair gene in a repair-deficient Chinese hamster ovary cell line (1987) (1)
In Vitro Correction of Cells from Patients with Mutagen Hypersensitivity (1989) (1)
Repair of uv-damaged DNA in normal human and xeroderma pigmentosum cells (1973) (1)
Synchronization of a Definite Number of Cells in Tissue Culture by Excess Thymidine Exposures (1967) (1)
DNA repair and mutagenesis: edited by E.C. Friedberg, G.C. Walker and W. Siede ASM Press, 1995. £79.00 hbk (698 pages) ISBN 1 55581 088 8 (1996) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1982) (1)
The role of the Philadelphia translocation in chronic myelocytic leukemia. (1987) (1)
42 Deficiencies in DNA repair and its clinical impacts (1995) (0)
Localization of the meningioma tumor suppressor gene using a translocation (1991) (0)
Mitotic dealy caused by irradiation at different phases of the generation cycle (1963) (0)
Transcription-coupled Repair as a Biodefence Mechanism (1998) (0)
Contents, Vol. 32, 1982 (1982) (0)
Mammalian blue-light photoreceptor homologs CRY1 and CRY2 are involved in maintenance of circadian rhythms (1999) (0)
Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1980) (0)
Breakpoint Analysis in CML: Potentials for Detection of Minimal Residual Disease (1986) (0)
S21 02 WA – GENES CONTROLLING DNA REPAIR IN MAMMALIAN CELLS (1991) (0)
Contents, Vol. 37, 1984 (1984) (0)
Subject Index Vol. 13, 1974 (1974) (0)
Human gene mapping 2 : Rotterdam Conference (1974) (1975) (0)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. (1976) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Summary of the Workshop on DNA Repair Defects (1987) (0)
The Role of the Ph Chromosome in Chronic Myelocytic Leukemia (1987) (0)
Author Index / Subject Index Vol. 49, 1988 (1988) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Establishment and Characterization of a Melanoma Cell Line from a Xeroderma Pigmentosum Patient : Activation of N-ras at a Potential Pyrimidine Dimer Site 1 (2006) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. (1976) (0)
Molecular and cellular basis of genome instability in cancer (1988) (0)
Oncogenes and Chromosomal Aberrations (1986) (0)
Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
Poster sessionGeneration of antibodies against the neurofibromatosis type 2 gene product utilising the synthetic peptide strategy (1994) (0)
Conserved Pattern ofAntisense Overlapping Transcription inthe Homologous HumanERCC-IandYeastRADIODNA Repair GeneRegions (1989) (0)
Catalog of mapped human gene markers. (1980) (0)
XerodermaPigmentosum Complementation GroupG Associated withCockayne Syndrome (1993) (0)
Cloning of the mouse “bcr” gene (1986) (0)
Partial Characterization of Genes and Gene Products Involved in Excision Repair of Human Cells (1985) (0)
[The determination of the complementation groups for the cells of patients with xeroderma pigmentosum and the Cockayne syndrome found in Russia]. (1996) (0)
Subject Index Vol. 32, 1982 (1982) (0)
Repair mechanisms in mamalian cells. (1974) (0)
[Gene therapy: from fiction to reality?]. (1987) (0)
ON HUMAN CHROMOSOMES BY USING CELL FUSION (1983) (0)
Cytogenetic Follow-up Studies of Patients with Acute Non-Lymphocytic Leukemia and Chronic Myeloid Leukemia (2008) (0)
Genetics-Expression of-human myeloid-associated surface antigens in human-mouse myeloid cell hybrids ( chronic myeloid leukemia / Philadelphia chromosome / monoclonal antibodies / chromosome 11 ) (2003) (0)
NF2 gene mutations in meningiomas and vestibular schwannomas (1994) (0)
GENES CONTROLLING NUCLEOTIDE EXCISION REPAIR IN MAMMALIAN CELLS (1992) (0)
ONCOGENES AND ANTI-ONCOGENES (1986) (0)
[Decreased survivability and a DNA repair defect in the cells of patients with xeroderma pigmentosum and Cockayne syndrome under the action of radiation and chemical mutagens]. (1997) (0)
Microarray analysis of the response of the genome upon exposure to UV using genetically defined mouse models for DNA repair (2001) (0)
Leaps in Treatment of High-risk Breast Cancer? Prove it! (1993) (0)
Contents, Vol. 18, 1977 (1977) (0)
Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. (1976) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
GENES CONTROLLING DNA REPAIR (1992) (0)
Contents, Vol. 13, 1974 (1974) (0)
Isolation and Characterization of Genes Involved in Mammalian Excision Repair (1989) (0)
Recombining DNA Damage Repair, Basal Transcription, and Human Syndromes (1997) (0)
Abnormal Regulation of DMA Replication and Increased Lethality in Ataxia Telangiectasia Cells Exposed to Carcinogenic Agents 1 (2006) (0)
Spatio-temporally restricted expression of the cellular retinoic acid binding protein in the developing embryo (1989) (0)
Genetic heterogeneity in patients having ataxia telangiectasia (1982) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Molecular Cloning andBiological Characterization oftheHuman Excision Repair GeneERCC-3 (1990) (0)
Assignment of the AK 1 : Np : ABO linkage group to human chromosome 9 ( somatic cell hybrids / enzyme markers / gene localization ) (0)
Chanfes in the cell-cycle of mammalian cells induced by ultra-violet light (1967) (0)
References to the committee reports (1975) (0)
Regional localization of a beta-galactosidase locus on human chromosome 22. (1977) (0)
Conference report: 10th International Congress of Radiation Research, Würzburg, Germany, August 27-September 1, 1995. (1996) (0)
Third International Congress of Histochemistry and Cytochemistry: August 18–22, 1968, New York, N.Y. (1968) (0)
Establishment and Characterization of a Melanoma Cell Line from a Xeroderma Pigmentosum Patient: Activation of N-ras at a Potential Pyrimidine Dimer Site1 (2006) (0)
The role of the c-abl oncogene in Philadelphia chromosome positive chronic myelogenous leukaemia (1987) (0)
Human Genetic Mutant Cell Repository Index Vol. 18, 1977 (1977) (0)
68 Conservation of the rad21 Schizosaccharomyces pombe DNA double-strand break repair gene in mammals (1996) (0)
Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. (1976) (0)
Assignment of structural beta-galactosidase loci to human chromosomes 3 and 22. (1979) (0)
Nucleotide excision repair, transcription and human repair syndromes (1993) (0)

This paper list is powered by the following services:

Other Resources About Dirk Bootsma

en.wikipedia.org

What Schools Are Affiliated With Dirk Bootsma?

Dirk Bootsma is affiliated with the following schools: