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Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients

Journal of investigative dermatology, 2002-06, Vol.118 (6), p.972-982

2002

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A Stop Codon in Xeroderma Pigmentosum Group C Families in Turkey and Italy: Molecular Genetic Evidence for a Common Ancestor

Journal of investigative dermatology, 2001-08, Vol.117 (2), p.197-204

2001

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Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

Journal of investigative dermatology, 2008-08, Vol.128 (8), p.2055-2068

2008

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Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

Carcinogenesis (New York), 2006-01, Vol.27 (1), p.84-94

2006

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Increased ultraviolet sensitivity and chromosomal instability related to P53 function in the xeroderma pigmentosum variant

Cancer research (Chicago, Ill.), 1999-03, Vol.59 (5), p.1102-1108

1999

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The Human XRCC9 Gene Corrects Chromosomal Instability and Mutagen Sensitivities in CHO UV40 Cells

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (17), p.9232-9237

1997

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Clinical, Cellular, and Molecular Features of an Israeli Xeroderma Pigmentosum Family with a Frameshift Mutation in the XPC Gene: Sun Protection Prolongs Life

Journal of investigative dermatology, 2000-12, Vol.115 (6), p.974-980

2000

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Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B ( CSB) Gene

American journal of human genetics, 2000-04, Vol.66 (4), p.1221-1228

2000

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Phenotype of FAECB (Facility for Automated Experiments in Cell Biology) Chinese hamster ovary mutants with minimal UV-sensitivity

Mutation research, 2001-11, Vol.487 (1-2), p.31-39

2001

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Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients1

Journal of investigative dermatology, 2002-06, Vol.118 (6), p.972

2002

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Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4

Mutation research, 1997-03, Vol.383 (2), p.91-106

1997

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Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients11An abstract of this study was presented at the annual meeting of the Society for Investigative Dermatology, May 2000, Chicago, IL, and published in J Invest Dermatol 114:825, 2000

Journal of investigative dermatology, 2002-06, Vol.118 (6), p.972-982

2002

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Radiation and chemotherapy injury: pathophysiology, diagnosis, and treatment

Critical reviews in oncology/hematology, 1993-08, Vol.15 (1), p.49-89

Busch, David B.

1993

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Rectal foreign bodies: case reports and a comprehensive review of the world's literature

Surgery, 1986-09, Vol.100 (3), p.512-519

1986

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Genetic Diversity of UV-Sensitive DNA Repair Mutants of Chinese Hamster Ovary Cells

Proceedings of the National Academy of Sciences - PNAS, 1981-06, Vol.78 (6), p.3734-3737

1981

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Recontacting Subjects in Mutagen Exposure Monitoring Studies

IRB, 1986-11, Vol.8 (6), p.1-4

1986

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Follow-up: Recontacting Subjects in Mutagen Exposure Monitoring Studies

IRB, 1988-09, Vol.10 (5), p.9-11

1988

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Human cells with multiple monosomies. An overlooked resource for readily isolating cells with autosomal recessive mutations?

Mutagenesis, 1989-11, Vol.4 (6), p.486-486

Busch, D B

1989

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Presence and measurement of sample histidine in the ames test: Quantification and possible elimination of a source of false-positive mutagenicity test results

Environmental and molecular mutagenesis, 1987, Vol.10 (4), p.397-410

1987

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Recontacting subjects in mutagen-exposure-monitoring studies: II. Results of a questionnaire study of mutagenesis researchers, with review of the pertinent literature

Environmental and molecular mutagenesis, 1988, Vol.11 (3), p.333-358

1988

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Large-scale isolation of UV-sensitive clones of CHO cells

Somatic Cell Genetics, 1980-05, Vol.6 (3), p.407-418

1980

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Collection, Handling, and Disposal of Mutagenic Urine Specimens

IRB, 1989-09, Vol.11 (5), p.11-11

1989

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Drowning of a Friedreich's ataxia patient

The American journal of forensic medicine and pathology, 1987-03, Vol.8 (1), p.64-67

1987

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A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity

Mutation research, 1996-08, Vol.363 (3), p.209-221

1996

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Urine recovery experiments with quercetin and other mutagens using the ames test

Environmental mutagenesis, 1986, Vol.8 (3), p.393-399

1986

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Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients

A Stop Codon in Xeroderma Pigmentosum Group C Families in Turkey and Italy: Molecular Genetic Evidence for a Common Ancestor

Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

Increased ultraviolet sensitivity and chromosomal instability related to P53 function in the xeroderma pigmentosum variant

The Human XRCC9 Gene Corrects Chromosomal Instability and Mutagen Sensitivities in CHO UV40 Cells

Clinical, Cellular, and Molecular Features of an Israeli Xeroderma Pigmentosum Family with a Frameshift Mutation in the XPC Gene: Sun Protection Prolongs Life

Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B ( CSB) Gene

Phenotype of FAECB (Facility for Automated Experiments in Cell Biology) Chinese hamster ovary mutants with minimal UV-sensitivity

Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients1

Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4

Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients11An abstract of this study was presented at the annual meeting of the Society for Investigative Dermatology, May 2000, Chicago, IL, and published in J Invest Dermatol 114:825, 2000

Radiation and chemotherapy injury: pathophysiology, diagnosis, and treatment

Rectal foreign bodies: case reports and a comprehensive review of the world's literature

Genetic Diversity of UV-Sensitive DNA Repair Mutants of Chinese Hamster Ovary Cells

Recontacting Subjects in Mutagen Exposure Monitoring Studies

Follow-up: Recontacting Subjects in Mutagen Exposure Monitoring Studies

Human cells with multiple monosomies. An overlooked resource for readily isolating cells with autosomal recessive mutations?

Presence and measurement of sample histidine in the ames test: Quantification and possible elimination of a source of false-positive mutagenicity test results

Recontacting subjects in mutagen-exposure-monitoring studies: II. Results of a questionnaire study of mutagenesis researchers, with review of the pertinent literature

Large-scale isolation of UV-sensitive clones of CHO cells

Collection, Handling, and Disposal of Mutagenic Urine Specimens

Drowning of a Friedreich's ataxia patient

A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity

Urine recovery experiments with quercetin and other mutagens using the ames test

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