J. Robbins

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DNA repair in human fibroblasts, as reflected by host-cell reactivation of a transfected UV-irradiated luciferase gene, is not related to donor age.

R. Tarone, P. J. Brooks, T. Merkle, 2004, Mutation research.

Gene specific DNA repair of damage induced in familial Alzheimer disease cells by ultraviolet irradiation or by nitrogen mustard.

C. Link, V. Bohr, J. Robbins, 1995, Mutation research.

Inherent inability of chronic lymphocytic leukaemia lymphocytes to respond to phytohaemagglutinin.

J. Robbins, W. Levis, 1972, International archives of allergy and applied immunology.

Induction by ionizing radiation of the gadd45 gene in cultured human cells: lack of mediation by protein kinase C.

A. Fornace, O. Mcbride, I. Hickson, 1991, Molecular and cellular biology.

DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.

I. Rapin, J. Hoeijmakers, W. Vermeulen, 1996, The Journal of investigative dermatology.

Ultraviolet-stimulated thymidine incorporation in xeroderma pigmentosum lymphocytes.

M. Lutzner, J. Robbins, P. Burk, 1971, The Journal of laboratory and clinical medicine.

RELATION OF D.N.A. REPAIR PROCESSES TO PATHOLOGICAL AGEING OF THE NERVOUS SYSTEM IN XERODERMA PIGMENTOSUM

J. Robbins, A. Andrews, S. Barrett, 1976, The Lancet.

Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates.

K. Kraemer, H. Coon, J. Robbins, 1975, Proceedings of the National Academy of Sciences of the United States of America.

RADIOSENSITIVITY IN ALZHEIMER DISEASE AND PARKINSON DISEASE

R. Tarone, F. Otsuka, R. Brumback, 1983, The Lancet.

Gene-specific DNA repair in xeroderma pigmentosum complementation groups A, C, D, and F. Relation to cellular survival and clinical features.

M. Evans, R. Tarone, V. Bohr, 1993, The Journal of biological chemistry.

Typical xeroderma pigmentosum complementation group A fibroblasts have detectable ultraviolet light-induced unscheduled DNA synthesis.

R. Tarone, J. Robbins, A. Andrews, 1977, Biochimica et biophysica acta.

Colony-forming ability of ultraviolet-irradiated xeroderma pigmentosum fibroblasts from different DNA repair complementation groups.

K. Kraemer, J. Robbins, A. Andrews, 1976, Biochimica et biophysica acta.

Five complementation groups in xeroderma pigmentosum.

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

Evidence for defective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells.

R. Tarone, K. Kraemer, J. Robbins, 1991, Mutation research.

Cockayne syndrome and xeroderma pigmentosum

I. Rapin, K. Kraemer, J. Robbins, 2000, Neurology.

Xeroderma pigmentosum. Defective DNA repair causes skin cancer and neurodegeneration.

J. Robbins, 1988, JAMA.

Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in fibroblasts from patients with Huntington disease, familial dysautonomia, and other primary neuronal degenerations.

D. Scudiero, R. Tarone, S. Meyer, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation.

J. Robbins, A. Andrews, S. Barrett, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Cockayne's syndrome fibroblasts have increased sensitivity to ultraviolet light but normal rates of unscheduled DNA synthesis.

J. Robbins, A. Andrews, S. Barrett, 1978, The Journal of investigative dermatology.

Fluorescent light-induced chromatid breaks distinguish Alzheimer disease cells from normal cells in tissue culture.

M. Schapiro, R. Parshad, R. Tarone, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Skin cancer and chromosomal aberrations induced by ultraviolet radiation. Evidence for lack of correlation in xeroderma pigmentosum variant and group E patients.

R. Tarone, J. Robbins, M. Ganges, 1992, Cancer genetics and cytogenetics.

A Childhood Neurodegeneration Due to Defective DNA Repair: A Novel Concept of Disease Based on Studies of Xeroderma Pigmentosum

J. Robbins, 1989, Journal of child neurology.

No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H

J. Robbins, 1989, Human Genetics.

Xeroderma pigmentosum long-term lymphoid lines with increased ultraviolet sensitivity.

K. Kraemer, D. Buell, J. Robbins, 1974, Journal of the National Cancer Institute.

Induction by ionizing radiation of the gadd45 gene in cultured human cells: lack of mediation by protein kinase C

O. Mcbride, A. Fornace, I. Alamo, 1991 .

Clinically asymptomatic xeroderma pigmentosum neurological disease in an adult: evidence for a neurodegeneration in later life caused by defective DNA repair.

R. Brumback, A. Moshell, J. Robbins, 1993, European neurology.

Adult-onset xeroderma pigmentosum neurological disease--observations in an autopsy case.

S. Merchant, R. Brumback, K. Kraemer, 2002, Clinical neuropathology.

Hypersensitivity to DNA-damaging agents in abiotrophies: a new explanation for degeneration of neurons, photoreceptors, and muscle in Alzheimer, Parkinson and Huntington diseases, retinitis pigmentosa, and Duchenne muscular dystrophy.

D. Scudiero, R. Tarone, F. Otsuka, 1985, Basic life sciences.

FUNCTION OF GLASS-ADHERENT CELLS IN HUMAN MIXED LYMPHOCYTE CULTURES

J. Robbins, W. Levis, 1970 .

DNA repair disorders with overlaps and paradoxes

I. Rapin, K. Kraemer, J. Robbins, 2000 .

Use of lymphoblastoid cell lines to evaluate the hypersensitivity to ultraviolet radiation in Cockayne syndrome.

R. Tarone, F. Otsuka, J. Robbins, 1984, The Journal of investigative dermatology.

Parkinson's disease, twins, and the DNA‐damage hypothesis

J. Robbins, 1987, Annals of neurology.

Ultraviolet light-induced sister chromatid exchanges in xeroderma pigmentosum and in Cockayne's syndrome lymphocyte cell lines.

J. Whang‐Peng, R. Tarone, J. Robbins, 1978, Cancer research.

The Oxidative DNA Lesion 8,5′-(S)-Cyclo-2′-deoxyadenosine Is Repaired by the Nucleotide Excision Repair Pathway and Blocks Gene Expression in Mammalian Cells*

R. Tarone, M. Smerdon, P. J. Brooks, 2000, The Journal of Biological Chemistry.

Ionizing-radiation-induced damage in the DNA of cultured human cells. Identification of 8,5-cyclo-2-deoxyguanosine.

M. Dizdaroglu, J. Robbins, M. Dirksen, 1987, The Biochemical journal.

Xeroderma Pigmentosum: An Inherited Disease with Sun Sensitivity, Multiple Cutaneous Neoplasms, and Abnormal DNA Repair

K. Kraemer, H. Coon, M. Lutzner, 1974 .

The post-UV colony-forming ability of normal fibroblast strains and of the xeroderma pigmentosum group G strain.

R. Tarone, A. Moshell, J. Robbins, 1981, The Journal of investigative dermatology.

Repair of DNA in xeroderma pigmentosum conjunctiva.

K. Kraemer, D. Newsome, J. Robbins, 1975, Archives of ophthalmology.

Xeroderma pigmentosum and D. N. A. repair.

S. Yuspa, M. Lutzner, J. Robbins, 1971, Lancet.

Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell lines.

R. Tarone, F. Otsuka, R. Brumback, 1985, Journal of neurology, neurosurgery, and psychiatry.

Lymphoblastoid lines and skin fibroblasts from patients with tuberous sclerosis are abnormally sensitive to ionizing radiation and to a radiomimetic chemical.

D. Scudiero, R. Tarone, S. Meyer, 1982, The Journal of investigative dermatology.

RADIOSENSITIVITY IN HUNTINGTON'S DISEASE: IMPLICATIONS FOR PATHOGENESIS AND PRESYMPTOMATIC DIAGNOSIS

R. Tarone, A. Moshell, J. Robbins, 1980, The Lancet.

Methods for obtaining purified lymphocytes, glass-adherent mononuclear cells, and a population containing both cell types from human peripheral blood.

J. Robbins, W. Levis, 1972, Blood.

Relationship of DNA repair to carcinogenesis in xeroderma pigmentosum.

J. Robbins, P. Burk, 1973, Cancer research.

Hypersensitivity to ionizing radiation in cultured cells from down syndrome patients

R. Tarone, F. Otsuka, J. Robbins, 1985, Journal of the Neurological Sciences.

HOST CELL REACTIVATION BY FIBROBLASTS FROM PATIENTS WITH PIGMENTARY DEGENERATION OF THE RETINA

R. Tarone, J. Robbins, S. Barrett, 1983, Photochemistry and photobiology.

DNA repair processes protect human beings from premature solar skin damage: evidence from studies on xeroderma pigmentosum.

A. Moshell, J. Robbins, 1979, The Journal of investigative dermatology.

Abnormal rate and duration of ultraviolet-induced thymidine incorporation into lymphocytes from patients with Xeroderma pigmentosum and associated neurological complications.

K. Kraemer, J. Robbins, 1972, Mutation research.

Rapid and sensitive assay for D.N.A. synthesis in leucocyte cultures.

J. Robbins, W. Levis, P. Burk, 1970, Lancet.

Effect of glass-adherent cells on the blastogenic response of 'purified' lymphocytes to phytohemagglutinin.

J. Robbins, W. Levis, 1970, Experimental cell research.

Prolonged ultraviolet-induced thymidine incorporation into xeroderma pigmentosum lymphocytes: studies on its duration, amount, localization and relationship to hydroxyurea.

K. Kraemer, J. Robbins, 1972, Biochimica et biophysica acta.

Significance of repair of human DNA: evidence from studies of xeroderma pigmentosum.

J. Robbins, 1978, Journal of the National Cancer Institute.

Xeroderma pigmentosum epidermal cells with normal UV-induced thymidine incorporation.

J. Robbins, W. Levis, A. E. Miller, 1972, The Journal of investigative dermatology.

Incorrect priority claim for the DNA-damage hypothesis.

J. Robbins, 1987, Archives of neurology.

DNA repair in tumor cells from the variant form of xeroderma pigmentosum.

B. Flaxman, K. Kraemer, J. Robbins, 1975, The Journal of investigative dermatology.

Effects of DNA-damaging agents on Down syndrome cells: implications for defective DNA-repair mechanisms.

R. Tarone, J. Robbins, K. Liao, 1987, Progress in clinical and biological research.

Radiosensitive Down syndrome lymphoblastoid lines have normal ionizing-radiation-induced inhibition of DNA synthesis.

R. Tarone, C. Hauser, J. Robbins, 1988, Mutation research.

A sensitive assay for detecting hypersensitivity to ionizing radiation in lymphoblastoid lines from patients with duchenne muscular dystrophy and primary neuronal degenerations

R. Tarone, F. Otsuka, J. Robbins, 1984, Journal of the Neurological Sciences.

Hypersensitivity to DNA-damaging agents in cultured cells from patients with Usher's syndrome and Duchenne muscular dystrophy.

D. Scudiero, R. Tarone, F. Otsuka, 1984, Journal of neurology, neurosurgery, and psychiatry.

Statistical methods for in vitro cell survival assays.

D. Scudiero, R. Tarone, J. Robbins, 1983, Mutation research.

Evidence that lack of deoxyribonucleic acid repair causes death of neurons in xeroderma pigmentosum

J. Robbins, Ronald J. Polinsky, Alan N. Moshell, 1983, Annals of neurology.

Normal pressure hydrocephalus. Recognition and relationship to neurological abnormalities in Cockayne's syndrome.

R. Brumback, G. Peck, J. Robbins, 1978, Archives of neurology.

Alzheimer's disease fibroblasts have normal repair of N-methyl-N'-nitro-N-nitrosoguanidine-induced DNA damage determined by the alkaline elution technique.

A. Fornace, T. Kinsella, J. Robbins, 1987, Biochemical and biophysical research communications.

Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical.

D. Scudiero, R. Tarone, R. Brumback, 1986, Mutation research.

Cockayne Syndrome: Clinicopathologic and Tissue Culture Studies of Affected Siblings

R. Tarone, F. Otsuka, R. Brumback, 1985, Journal of neuropathology and experimental neurology.

DNA REPAIR NUCLEOTIDE SEQUENCES WHICH PREVENT PREMATURE DEATH OF NEURONS IN HUMANS: EVIDENCE FROM STUDIES ON XERODERMA PIGMENTOSUM

A. Moshell, J. Robbins, A. Andrews, 1978 .

Ultraviolet light-induced chromosomal aberrations in cultured cells from Cockayne syndrome and complementation group C xeroderma pigmentosum patients: lack of correlation with cancer susceptibility.

R. Tarone, J. Robbins, K. Liao, 1988, American journal of human genetics.

A simple and rapid method for evaluating the survival of xeroderma pigmentosum lymphoid lines after irradiation with ultraviolet light

R. Tarone, A. Moshell, J. Robbins, 1981, In Vitro.

NEW FORMS OF DISEASES WITH DNA REPAIR DEFECTS

J. Robbins, 1979, Photochemistry and photobiology.

Radiation sensitivity of fibroblast strains from patients with Usher's syndrome, Duchenne muscular dystrophy, and Huntington's disease.

R. Tarone, J. Little, J. Robbins, 1987, Mutation research.

The millipore filter assay technique for measuring tritiated thymidine incorporation into DNA in leucocyte cultures.

J. Gart, J. Robbins, W. Levis, 1972, Clinical and experimental immunology.

A 32P-Postlabeling Assay for the Oxidative DNA Lesion 8,5′-Cyclo-2′-deoxyadenosine in Mammalian Tissues

P. J. Brooks, G. Zhou, K. Randerath, 2001, The Journal of Biological Chemistry.

Human fibroblast strain with normal survival but abnormal postreplication repair after ultraviolet light irradiation.

J. Doniger, J. Robbins, S. Barrett, 1980, Cancer research.

Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D

J. Robbins, 1991, Human Genetics.

Chapter 10 – Xeroderma Pigmentosum

J. Robbins, 1987 .

The Cockayne syndrome--an inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA. Comparison with xeroderma pigmentosum.

F. Otsuka, J. Robbins, 1985, The American Journal of dermatopathology.

Neurological disease in xeroderma pigmentosum. Documentation of a late onset type of the juvenile onset form.

J. Carl, M. Denckla, L. Gerber, 1991, Brain : a journal of neurology.

Complementing xeroderma pigmentosum fibroblasts restore biological activity to UV-damaged DNA.

R. Day, K. Kraemer, J. Robbins, 1975, Mutation research.

Contents, Vol. 39, 1970

F. Hecht, R. Winkelmann, A. M. Davies, 1970 .

Identification of the novel lesion 8,5'-cyclo-2'-deoxyguanosine in DNA isolated from. gamma. -irradiated human cells

M. Dizdaroglu, J. Robbins, M. Simic, 1986 .

Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases.

D. Dickson, I. Rapin, K. Kraemer, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

THE RELATIONSHIP BETWEEN NEUROLOGIC DISEASE, ACUTE SUN SENSITIVITY, AND POST-ULTRAVIOLET COLONY-FORMING ABILITY IN XERODERMA PIGMENTOSUM

J. Robbins, A. Andrews, S. Barrett, 1978 .