D. Bootsma

J. Hoeijmakers, W. Vermeulen, G. V. D. van der Horst, 1998, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

Recombining DNA Damage Repair, Basal Transcription, and Human Syndromes

J. Hoeijmakers, W. D. Laat, W. Vermeulen, 1997 .

Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein.

S. Keeney, T. Brody, J. Hoeijmakers, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

S. Humbert, J. Hoeijmakers, W. Vermeulen, 1994, The EMBO journal.

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.

R. Gatti, C. Baan, D. Bootsma, 1988, Cytogenetics and cell genetics.

UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice.

S. Velasco-Miguel, J. Hoeijmakers, J. Richardson, 2002, DNA repair.

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas.

A. Hagemeijer, C. Avezaat, B. Seizinger, 1994, American journal of human genetics.

A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene.

A. Hagemeijer, E. Zwarthoff, C. Avezaat, 1991, American journal of human genetics.

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

R. Scott, J. Hoeijmakers, W. Vermeulen, 1994, American journal of human genetics.

Mutational analysis of the human nucleotide excision repair gene ERCC1.

P. J. van der Spek, J. Hoeijmakers, D. Bootsma, 1996, Nucleic acids research.

Unscheduled DNA synthesis in xeroderma pigmentosum cells after microinjection of yeast photoreactivating enzyme.

W. Vermeulen, A. Eker, D. Bootsma, 1986, Mutation research.

Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids.

A. Hagemeijer, D. Bootsma, A. von dem Borne, 1983, Proceedings of the National Academy of Sciences of the United States of America.

The genetic defect in the de Sanctis-Cacchione syndrome.

V. D. Der Kaloustian, D. Bootsma, W. Kleijer, 1974, The Journal of investigative dermatology.

International system for human gene nomenclature (1979) ISGN (1979).

N E Morton, T H Roderick, P J McAlpine, 1979, Cytogenetics and cell genetics.

International System for Human Gene Nomenclature (1979) ISGN (1979).

N E Morton, T H Roderick, P J McAlpine, 1980, Birth defects original article series.

Improved identification of chromosomes of leukemic cells in methotrexate-treated cultures.

A. Hagemeijer, D. Bootsma, E. Smit, 1979, Cytogenetics and cell genetics.

Incorporation of isolated chromosomes and induction of hypoxanthine phosphoribosyltransferase in chinese hamster cells

D. Bootsma, J. Horst, G. Wullems, 1975, Somatic cell genetics.

Claim that two human linkage groups carry different loci for GPT and LDH withdrawn

D. Bootsma, A. Westerveld, P. Khan, 1974, Nature.

α-Galactosidase in man-Chinese hamster somatic cell hybrids

D. Bootsma, A. Westerveld, P. Khan, 1975 .

Expression of human hypoxanthine phosphoribosyl transferase in Chinese hamster cells treated with isolated human chromosomes

D. Bootsma, J. Horst, G. Wullems, 1976, Somatic cell genetics.

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

D. Bootsma, H. Someren, W. Burgerhout, 2004, Humangenetik.

Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.

H. Galjaard, A. Reuser, A. Hoogeveen, 1974, Experimental cell research.

Transfer of the human genes coding for thymidine kinase and galactokinase to Chinese hamster cells and human-Chinese hamster cell hybrids

D. Bootsma, J. Horst, G. Wullems, 1977, Somatic cell genetics.

Synteny of the human loci for fumarate hydratase and udpg pyrophosphorylase with chromosome 1 markers in somatic cell hybrids.

D. Bootsma, A. Westerveld, H. van Someren, 1974, Cytogenetics and cell genetics.

Assignment of the AK1:Np:ABO linkage group to human chromosome 9.

A. Jongsma, D. Bootsma, A. Westerveld, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Molecular cloning and biological characterization of the human excision repair gene ERCC-3

J. Hoeijmakers, R. V. van Ham, A. van der Eb, 1990, Molecular and cellular biology.

Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

J. Hoeijmakers, W. Vermeulen, J. Jaeken, 1993, American journal of human genetics.

c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia

J. Stephenson, N. Heisterkamp, J. Groffen, 1983, The Journal of experimental medicine.

Genetical studied on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids.

P. Pearson, D. Bootsma, A. Westerveld, 1974, Human heredity.

Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6.

J. Hoeijmakers, L. Prakash, S. Prakash, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.

J. Garssen, J. Hoeijmakers, H. van Steeg, 1999, Cancer research.

Genes controlling nucleotide excision repair in eukaryotic cells

J. Hoeijmakers, D. Bootsma, G. Weeda, 1993, BioEssays : news and reviews in molecular, cellular and developmental biology.

XerodermaPigmentosum Complementation GroupG Associated withCockayne Syndrome

W. Vermeulen, H. J. Hoeijmakers, J. Jaeken, 1993 .

Xeroderma pigmentosum complementation group H falls into complementation group D.

S. Giliani, J. Hoeijmakers, W. Vermeulen, 1991, Mutation research.

A seventh complementation group in excision-deficient xeroderma pigmentosum.

P. J. Abrahams, D. Bootsma, C. Arlett, 1979, Mutation research.

Five complementation groups in xeroderma pigmentosum.

D. Bootsma, K. Kraemer, J. Robbins, 1975, Mutation research.

Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B.

J. Hoeijmakers, D. Bootsma, C. Troelstra, 1993, Nucleic acids research.

The genetic defect in DNA repair deficiency syndromes. EACR--Mühlbock Memorial Lecture, 1993.

D. Bootsma, Dirk Bootsma, 1993, European journal of cancer.

Isolation and Characterization of Genes Involved in Mammalian Excision Repair

A. Yasui, J. Hoeijmakers, D. Bootsma, 1989 .

Molecular Genetic Dissection of Mammalian Excision Repair

A. V. D. Eb, J. Hoeijmakers, D. Bootsma, 1989 .

Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line.

L. Roza, D. Bootsma, A. Westerveld, 1987, Mutation research.

The genetic basis of xeroderma pigmentosum.

J. Hoeijmakers, D. Bootsma, 1991, Annales de genetique.

Xeroderma pigmentosum complementation group XP-I withdrawn.

E. Jung, D. Bootsma, W. Keijzer, 1989, Mutation research.

Identification and characterization of XPC-binding domain of hHR23B

P. J. van der Spek, J. Hoeijmakers, K. Sugasawa, 1997, Molecular and cellular biology.

A ninth complementation group in xeroderma pigmentosum, XP I.

E. Jung, L. Edler, D. Bootsma, 1985, Mutation research.

Defective DNA Repair and Cancer

D. Bootsma, 1977 .

UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes.

D. Bootsma, J. de Wit, W. Kleijer, 1973, Mutation research.

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

J. Hoeijmakers, W. Vermeulen, D. Bootsma, 1992, Cell.

Nomenclature of human DNA repair genes.

R. Wood, L. Thompson, A. Lehmann, 1994, Mutation research.

The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.

J. Hoeijmakers, W. Vermeulen, D. Bootsma, 1989, Mutation research.

Constitutional DNA‐level aberrations in chromosome 22 in a patient with multiple meningiomas

T. H. van der Kwast, A. Hagemeijer, E. Zwarthoff, 1994, Genes, chromosomes & cancer.

Molecular Cloning andBiological Characterization oftheHuman Excision Repair GeneERCC-3

D. Bootsma, G. Weeda, A. Westerveld, 1990 .

Complementation analysis of xeroderma pigmentosum variants

D. Bootsma, N. Jaspers, Gerard van de Kuilen, 1981 .

Dhr6, a Drosophila homolog of the yeast DNA-repair gene RAD6.

J. Hoeijmakers, L. Prakash, S. Prakash, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation.

J. Cohen, D. Bootsma, M. Mulder, 1970, Mutation research.

Xeroderma pigmentosum group A correcting protein from calf thymus.

K. Tanaka, J. Hoeijmakers, W. Vermeulen, 1992, Mutation research.

GENES CONTROLLING NUCLEOTIDE EXCISION REPAIR IN MAMMALIAN CELLS

J. Hoeijmakers, W. Vermeulen, D. Bootsma, 1992 .

DNA repair: two pieces of the puzzle

J. Hoeijmakers, D. Bootsma, 1992, Nature Genetics.

A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A.

D. Bootsma, M. Sabour, J. Parrington, 1976, Mutation research.

Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23.

K. Tanaka, J. Hoeijmakers, K. Sugasawa, 1994, The EMBO journal.

GENES CONTROLLING DNA REPAIR

D. Bootsma, 1992 .

Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity

R. Wood, P. J. van der Spek, J. Hoeijmakers, 1997, Molecular and cellular biology.

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.

J. Hoeijmakers, L. Thompson, D. Bootsma, 1988, Mutation research.

Regional mapping of the human immunoglobulin lambda light chain to the Philadelphia chromosome in chronic myeloid leukaemia.

C. Bartram, G. Grosveld, A. de Klein, 1984, Leukemia research.

Establishment and Characterization of a Melanoma Cell Line from a Xeroderma Pigmentosum Patient: Activation of N-ras at a Potential Pyrimidine Dimer Site1

J. Hoeijmakers, J. Bos, D. Bootsma, 2006 .

Is the chromosomal region 9q34 always involved in variants of the Ph1 translocation?

A. Hagemeijer, C. Bartram, D. Bootsma, 1984, Cancer genetics and cytogenetics.

The Role of the Ph Chromosome in Chronic Myelocytic Leukemia

N. Heisterkamp, J. Groffen, G. Grosveld, 1987 .

Breakpoint Analysis in CML: Potentials for Detection of Minimal Residual Disease

N. Heisterkamp, J. Groffen, G. Grosveld, 1986 .

Replication pattern of the X chromosomes in three X/autosomal translocations.

A. Hagemeijer, D. Bootsma, J. Hoovers, 1977, Cytogenetics and cell genetics.

Synchronization of mammalian cells in vitro by inhibition of the DNA synthesis. I. Optimal conditions.

D. Bootsma, H. Schenk, G. Galavazi, 1966, Experimental cell research.

Genomic characterization of the human DNA excision repair gene ERCC-1.

J. Hoeijmakers, P. ten Dijke, D. Bootsma, 1987, Nucleic acids research.

The influence of 5-bromodeoxyuridine on the induction of breaks in the deoxyribonucleic acid of cultivated human cells by x-irradiation and ultraviolet light.

D. Bootsma, P. Lohman, A. Hey, 1972, Radiation research.

CHANGES INDUCED IN THE FIRST POST-IRRADIATION GENERATION CYCLE OF HUMAN CELLS STUDIES BY DOUBLE LABELING.

D. Bootsma, 1965, Experimental cell research.

Microinjected photoreactivating enzymes from Anacystis and Saccharomyces monomerize dimers in chromatin of human cells.

A. Yasui, J. Hoeijmakers, W. Vermeulen, 1985, Mutation research.

Expression of human hprt gene on the inactive X chromosome after DNA-mediated gene transfer

P. J. Abrahams, D. Bootsma, A. Westerveld, 1982, Nature.

Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia

N. Heisterkamp, J. Groffen, G. Grosveld, 1987, Cell.

Molecular Cloning of the Human DNA Excision Repair

L. Thompson, D. Bootsma, C. Troelstra, 2022 .

Third International Congress of Histochemistry and Cytochemistry: August 18–22, 1968, New York, N.Y.

W. D. Selles, W. W. Doane, J. E. Kephart, 1968 .

Third International Congress of Histochemistry and Cytochemistry

Richard E. Cornell, W. D. Selles, W. W. Doane, 1968 .

Induction of sister chromatid exchanges in xeroderma pigmentosum cells after exposure to ultraviolet light.

D. Bootsma, G. Rainaldi, W. Keijzer, 1977, Mutation research.

Clinical characteristics, DNA repair, and complementation groups in xeroderma pigmentosum patients from Egypt.

G. Thomas, D. Bootsma, J. Cleaver, 1980, Cancer research.

Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation.

M. Paterson, A. Lehmann, D. Bootsma, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Xeroderma pigmentosum: biochemical and genetic characteristics.

D. Bootsma, J. Cleaver, 1975, Annual review of genetics.

Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma.

P H Riegman, P. D. de Jong, P. Riegman, 1995, Oncogene.

Phenotypic correction of the defect in xeroderma pigmentosum cells after fusion with isolated cytoplasts.

D. Bootsma, A. Verkerk, W. Keijzer, 1982, Experimental cell research.

Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion.

D. Bootsma, N. Jaspers, 1982, Proceedings of the National Academy of Sciences of the United States of America.

STUDIES ON SYNCHRONOUS DIVISION OF TISSUE CULTURE CELLS INITIATED BY EXCESS THYMIDINE.

D. Bootsma, O. Vos, L. Budke, 1964, Experimental cell research.

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

A. V. D. Eb, J. Hoeijmakers, W. Vermeulen, 1990, Cell.

Genetic heterogeneity of xeroderma pigmentosum demonstrated by somatic cell hybridization.

D. Bootsma, W. Keijzer, E. A. de Weerd-Kastelein, 1972, Nature: New biology.

Synchronization of mammalian cells in vitro by inhibition of the DNA synthesis. II. Population dynamics.

D. Bootsma, G. Galavazi, 1966, Experimental cell research.

Isolation of Chinese hamster ovary cells with reduced unscheduled DNA synthesis after UV irradiation

A. Reuser, D. Bootsma, M. Stefanini, 1982, Somatic cell genetics.

The progression of mammalian cells through the division cycle following ultraviolet irradiation.

R. Humphrey, D. Bootsma, 1968, Mutation research.

Repair of x-ray damage in DNA of cultivated cells from patients having xeroderma pigmentosum.

D. Bootsma, P. Lohman, W. Kleijer, 1970, Mutation research.

A third complementation group in xeroderma pigmentosum.

D. Bootsma, W. Keijzer, E. A. de Weerd-Kastelein, 1974, Mutation research.

Effects of inhibitors on repair of DNA in normal human and xeroderma pigmentosum cells after exposure to x-rays and ultraviolet irradiation.

D. Bootsma, W. Kleijer, M. Sluyter, 1973, Mutation research.

Repair mechanisms in mammalian cells

D. Bootsma, P. Lohman, 1974 .

Abnormal Regulation of DMA Replication and Increased Lethality in Ataxia Telangiectasia Cells Exposed to Carcinogenic Agents 1

M. Regulski, D. Bootsma, N. Jaspers, 2006 .

Abnormal regulation of DNA replication and increased lethality in ataxia telangiectasia cells exposed to carcinogenic agents.

M. Regulski, D. Bootsma, J. de Wit, 1982, Cancer research.

Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair

D. Bootsma, N. Jaspers, J. Boué, 1979, Clinical genetics.

Human diseases with genetically altered DNA repair processes.

E. Friedberg, D. Bootsma, J. Cleaver, 1975, Genetics.

Normal chiasma formation in a male with xeroderma pigmentosum.

N. Skakkebaek, D. Bootsma, M. Hultén, 2009, Hereditas.

SYNTHESIS OF RIBONUCLEIC ACID IN REGENERATING RAT LIVER AFTER PARTIAL HEPATECTOMY.

D. Bootsma, W. Welling, Van Muiswinkel, 1965, Biochimica et biophysica acta.

The regulation of cell proliferation and differentiation in intestinal epithelium. II. A quantitative histochemical and autoradiographic study after low doses of x-irradiation.

H. Galjaard, D. Bootsma, 1969, Experimental cell research.

Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification

J. Hoeijmakers, J. Grootegoed, D. Bootsma, 1996, Cell.

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

J. Stephenson, A. Hagemeijer, N. Heisterkamp, 1982, Nature.

Genetic complementation analysis of xeroderma pigmentosum.

D. Bootsma, W. Kleijer, E. A. de Weerd-Kastelein, 1975, Basic life sciences.

The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation.

D. Bootsma, J. de Wit, N. Jaspers, 1981, Mutation research.

Repair of DNA damage after exposure to 4-nitroquinoline-1-oxide in heterokaryons derived from xeroderma pigmentosum cells.

D. Bootsma, B. Zelle, 1980, Mutation research.

Interaction of human and chick DNA repair functions in UV-irradiated xeroderma pigmentosum-chick erythrocyte heterokaryons.

D. Bootsma, G. Rainaldi, E. P. van der Veer, 1982, Experimental cell research.

XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes

Chikahide Masutani, Fumio Hanaoka, Peter J. van der Spek, 1996, Nucleic Acids Res..

Survival of excess thymidine synchronized cell populations in vitro after x-irradiation in various phases of the cell cycle.

D. Bootsma, O. Vos, H. Schenk, 1966, International journal of radiation biology and related studies in physics, chemistry, and medicine.

Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous Recombination

J. Hoeijmakers, R. Kanaar, J. Essers, 1997, Cell.

Evolution and mutagenesis of the mammalian excision repair gene ERCC-1.

J. Hoeijmakers, D. Meijer, D. Bootsma, 1988, Nucleic acids research.

Conserved pattern of antisense overlapping transcription in the homologous human ERCC-1 and yeast RAD10 DNA repair gene regions

J. Hoeijmakers, Satya Prakash, L. Prakash, 1989, Molecular and cellular biology.

Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10

A. Yasui, J. Hoeijmakers, D. Bootsma, 1986, Cell.

Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia

J. Stephenson, A. Hagemeijer, M. Ferguson-Smith, 1983, Nature.

Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line

G. Lenoir, C. Turc‐Carel, G. Grosveld, 1985, Molecular and cellular biology.

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.

F. Ruddle, D. Bootsma, 1978, Cytogenetics and cell genetics.

Preferential expression of cellular retinoic acid binding protein in a subpopulation of neural cells in the developing mouse embryo.

C. Mummery, A. V. van Kessel, D. Bootsma, 1989, Differentiation; research in biological diversity.

Translocation t(6;9) in acute non-lymphocytic leukaemia results in the formation of a DEK-CAN fusion gene.

M. Fornerod, A. Hagemeijer, G. Grosveld, 1992, Bailliere's clinical haematology.

Oncogenes and Chromosomal Aberrations

A. Hagemeijer, D. Bootsma, 1986 .

Chromosome and DNA-mediated gene transfer in cultured mammalian cells.

D. Bootsma, A. D. de Jonge, 1984, International review of cytology.

The cellular retinoic-acid-binding protein is expressed in tissues associated with retinoic-acid-induced malformations.

A. V. van Kessel, D. Bootsma, J. Meijers, 1990, Development.

Establishment and Characterization of a Melanoma Cell Line from a Xeroderma Pigmentosum Patient : Activation of N-ras at a Potential Pyrimidine Dimer Site 1

J. Bos, J. Hoeijmakers, D. Bootsma, 2006 .

The Cockayne syndrome B protein, involved in transcription‐coupled DNA repair, resides in an RNA polymerase II‐containing complex

J. Hoeijmakers, A. Constantinou, W. Vermeulen, 1997, The EMBO journal.

Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential pyrimidine dimer site.

J. Bos, J. Hoeijmakers, D. Bootsma, 1989, Cancer research.

Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function

A. Jochemsen, J. Hoeijmakers, A. van der Eb, 1994, Molecular and cellular biology.

DNA repair defects in genetic diseases in man.

D. Bootsma, 1979, Biochimie.

Loss of human genetic markers in man--Chinese hamster somatic cell hybrids.

D. Bootsma, A. Westerveld, P. Khan, 1971, Nature: New biology.

The Role of the Philadelphia Translocation in Chronic Myelocytic Leukemia

N. Heisterkamp, J. Groffen, G. Grosveld, 1987, Annals of clinical research.

Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition

F. Gruijl, H. Morreau, J. Hoeijmakers, 1997, Cell.

Report of the Committee on the Genetic Constitution of Chromosomes 2, 3, 4, and 5.

D. Bootsma, P. McAlpine, Kenneth K. Kidd, 1984, Cytogenetics and cell genetics.

Sequence conservation of the rad21 Schizosaccharomyces pombe DNA double-strand break repair gene in human and mouse.

A. Hagemeijer, M. McKay, P. J. van der Spek, 1996, Genomics.

RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.

Jaap, J. Hoeijmakers, D. Bootsma, 1994, The EMBO journal.

Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23.

A. Hagemeijer, P. J. van der Spek, J. Hoeijmakers, 1996, Genomics.

X-Linkage of Human α-Galactosidase

K. Grzeschik, G. Romeo, D. Bootsma, 1972 .

Abstracts of meeting presentations (Part 3 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Abstracts of meeting presentations (Part 2 of 11)

R. L. Miller, D. Cox, K. Kidd, 1982 .

Molecular genetics of eukaryotic DNA excision repair.

J. Hoeijmakers, D. Bootsma, D Bootsma, 1990, Cancer cells.

Leaps in Treatment of High-risk Breast Cancer? Prove it!

D. Bootsma, 1993 .

Cytogenetics and Cell Genetics

H. Klinger, D. Bootsma, 2010 .

Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids.

P. Pearson, D. Bootsma, A. Westerveld, 1976, Cytogenetics and cell genetics.

Late-replicating ring X-chromosomes identified by r-banding after BrdU pulse

A. Hagemeijer, D. Bootsma, J. Hoovers, 1976, Human Genetics.

Abstract of papers presented at the second international workshop, May 2–6, 1976, Noordwijkerhout (The Netherlands)

D. Bootsma, P. Lohman, B. Bridges, 1977 .

Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome.

J. Hoeijmakers, A. van der Eb, D. Bootsma, 1991, Carcinogenesis.

Different rates of restoration of the repair capacity in complementing xeroderma pigmentosum cells after fusion.

D. Bootsma, F. Berends, W. Keijzer, 1981, Experimental cell research.

DNA repair. Engagement with transcription.

J. Hoeijmakers, D. Bootsma, D Bootsma, 1993, Nature.

Summary of the Workshop on DNA Repair Defects

D. Bootsma, 1987 .

In Vitro Correction of Cells from Patients with Mutagen Hypersensitivity

J. Hoeijmakers, W. Vermeulen, L. Roza, 1989 .

Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells.

D. Bootsma, M. Stefanini, A. Westerveld, 1985, Experimental cell research.

Identification of DNA repair genes in the human genome.

A. Yasui, J. Hoeijmakers, D. Bootsma, 1986, Cold Spring Harbor symposia on quantitative biology.

Abstracts of meeting presentations (Part 10 of 11)

R. L. Miller, D. Cox, K. Kidd, 1984 .

Inhibition of DNA synthesis in ataxia telangiectasia fibroblasts after exposure to DNA-damaging agents

M. James, A. Lehmann, D. Bootsma, 1982 .

Abnormal levels of UV-induced unscheduled DNA synthesis in ataxia telangiectasia cells after exposure to ionizing radiation.

D. Bootsma, N. Jaspers, 1982, Mutation research.

Genetic complementation analysis of ataxia telangiectasia by somatic cell fusion.

D. Bootsma, N. Jaspers, 1982, IARC scientific publications.

Assignment of structural β-galactosidase loci to human chromosomes 3 and 22

D. Bootsma, A. Westerveld, J. Wit, 1979, Human Genetics.

Mammalian cell culture studies

D. Bootsma, A. Westerveld, J. Wit, 1973 .

Abstracts of meeting presentations (Part 5 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations.

D. Bootsma, J. German, M. Niermeijer, 1984, American journal of human genetics.

RAPID DIAGNOSTIC TEST FOR ATAXIA TELANGIECTASIA

D. Bootsma, N. Jaspers, J. Wit, 1981, The Lancet.

Regional localization of aβ-galactosidase locus on human chromosome 22

A. Hagemeijer, D. Halley, D. Bootsma, 1977 .

Abstracts of meeting presentations (Part 11 of 11)

R. L. Miller, D. Cox, K. Kidd, 1984 .

X Linkage of Human Galactosidase

K. Grzeschik, G. Romeo, D. Bootsma, 1972, Nature.

Two new linkage groups in man, both carrying different loci for lactate dehydrogenase and glutamic-pyruvic transaminase.

D. Bootsma, A. Westerveld, P. Meera Khan, 1972, Nature: New biology.

DNA repair in human cells: from genetic complementation to isolation of genes.

J. Hoeijmakers, D. Bootsma, A. Westerveld, 1988, Cancer surveys.

ONCOGENES AND ANTI-ONCOGENES

D. Bootsma, 1986, Pediatric Research.

Transfer of the human X chromosome to human-Chinese hamster cell hybrids via isolated HeLa metaphase chromosomes

D. Bootsma, J. Horst, G. Wullems, 1976, Somatic cell genetics.

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.

W. Vermeulen, A. Lehmann, J. Egly, 1994, Cold Spring Harbor symposia on quantitative biology.

Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site.

A. Jochemsen, J. Hoeijmakers, A. Eb, 1992, Nucleic Acids Research.

Cloning of a putative meningioma tumor suppressor gene

P. Riegman, A. Hagemeijer, E. Zwarthoff, 1994 .

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

D. Bootsma, A. Westerveld, M. A. Freeke, 1972, Biochemical Genetics.

Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1.

D. Bootsma, M. Stefanini, A. Westerveld, 1987, Experimental cell research.

Assignment of the AK 1 : Np : ABO linkage group to human chromosome 9 ( somatic cell hybrids / enzyme markers / gene localization )

A. Jongsma, D. Bootsma, A. Westerveld, 2022 .

XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes

J. Hoeijmakers, K. Sugasawa, F. Hanaoka, 1996, Nucleic Acids Res..