Robbins JH - Search Results

1

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

Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH. Moriwaki S, et al. Among authors: robbins jh. J Invest Dermatol. 1996 Oct;107(4):647-53. doi: 10.1111/1523-1747.ep12584287. J Invest Dermatol. 1996. PMID: 8823375 Free article.

2

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

Robbins JH, Kraemer KH, Flaxman BA. Robbins JH, et al. J Invest Dermatol. 1975 Mar;64(3):150-5. doi: 10.1111/1523-1747.ep12533310. J Invest Dermatol. 1975. PMID: 1117174 Free article.

3

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.

Barrett SF, Robbins JH, Tarone RE, Kraemer KH. Barrett SF, et al. Among authors: robbins jh. Mutat Res. 1991 Nov;255(3):281-91. doi: 10.1016/0921-8777(91)90032-k. Mutat Res. 1991. PMID: 1719400

4

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

Day RS, Kraemer KH, Robbins JH. Day RS, et al. Among authors: robbins jh. Mutat Res. 1975 May;28(2):251-5. doi: 10.1016/0027-5107(75)90103-7. Mutat Res. 1975. PMID: 166304

5

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

Kraemer KH, Andrews AD, Barrett SF, Robbins JH. Kraemer KH, et al. Among authors: robbins jh. Biochim Biophys Acta. 1976 Aug 18;442(2):147-53. doi: 10.1016/0005-2787(76)90485-8. Biochim Biophys Acta. 1976. PMID: 953007

6

Repair of DNA in xeroderma pigmentosum conjunctiva.

Newsome DA, Kraemer KH, Robbins JH. Newsome DA, et al. Among authors: robbins jh. Arch Ophthalmol. 1975 Aug;93(8):660-2. doi: 10.1001/archopht.1975.01010020626012. Arch Ophthalmol. 1975. PMID: 1164219

7

Cockayne syndrome and xeroderma pigmentosum.

Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH. Rapin I, et al. Among authors: robbins jh. Neurology. 2000 Nov 28;55(10):1442-9. doi: 10.1212/wnl.55.10.1442. Neurology. 2000. PMID: 11185579 Free PMC article. Review.

8

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

Robbins JH, Kraemer KH, Merchant SN, Brumback RA. Robbins JH, et al. Clin Neuropathol. 2002 Jan-Feb;21(1):18-23. Clin Neuropathol. 2002. PMID: 11846040

9

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

Kraemer KH, Coon HG, Petinga RA, Barrett SF, Rahe AE, Robbins JH. Kraemer KH, et al. Among authors: robbins jh. Proc Natl Acad Sci U S A. 1975 Jan;72(1):59-63. doi: 10.1073/pnas.72.1.59. Proc Natl Acad Sci U S A. 1975. PMID: 164028 Free PMC article.

10

Five complementation groups in xeroderma pigmentosum.

Kraemer KH, De Weerd-Kastelein EA, Robbins JH, Keijzer W, Barrett SF, Petinga RA, Bootsma D. Kraemer KH, et al. Among authors: robbins jh. Mutat Res. 1975 Dec;33(2-3):327-40. doi: 10.1016/0027-5107(75)90208-0. Mutat Res. 1975. PMID: 1243579

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