Kenneth H Kraemer
Kraemer, Kenneth H.
VIAF ID: 50775652 (Personal)
Permalink: http://viaf.org/viaf/50775652
Preferred Forms
- 100 0 _ ‡a Kenneth H Kraemer
- 100 1 _ ‡a Kraemer, Kenneth H.
- 100 1 _ ‡a Kraemer, Kenneth H. (sparse)
- 100 1 _ ‡a Kraemer, Kenneth H.
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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BASE COMPOSITION OF RNA SYNTHESIZED DURING CLEAVAGE OF THE SEA URCHIN EMBRYO | |
Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiency | |
Chromosomal protein HMGN1 enhances the rate of DNA repair in chromatin | |
Clearing of melanoma in situ with intralesional interferon alfa in a patient with xeroderma pigmentosum | |
Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life | |
Complementing xeroderma pigmentosum fibroblasts restore biological activity to UV-damaged DNA | |
Cornifying Darier disease--a unique variant. II. Surgical treatment | |
Decreased thymidine incorporation in circulating leukocytes after treatment of psoriasis with psoralen and long-wave ultraviolet light | |
DNA repair and mutagenesis in Werner syndrome. | |
The DNA Repair Interest Group: a global village | |
Do not underestimate nucleotide excision repair: it predicts not only melanoma risk but also survival outcome. | |
Dysplastic naevi and cutaneous melanoma risk | |
Dysplastic nevi as precursors to hereditary melanoma | |
Dysplastic nevi on the scalp of prepubertal children from melanoma-prone families | |
Early onset of skin and oral cavity neoplasms in xeroderma pigmentosum | |
The effect of donor age on the processing of UV-damaged DNA by cultured human cells: reduced DNA repair capacity and increased DNA mutability | |
Expression of a transfected DNA repair gene (XPA) in xeroderma pigmentosum group A cells restores normal DNA repair and mutagenesis of UV-treated plasmids. | |
For the record: the history of precursors to malignant melanoma | |
Forty years of research on xeroderma pigmentosum at the US National Institutes of Health. | |
From proteomics to disease | |
Global contributions to the understanding of DNA repair and skin cancer | |
Growth and nutrition in children with trichothiodystrophy. | |
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy | |
Heritable genetic alterations in a xeroderma pigmentosum group G/Cockayne syndrome pedigree | |
Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population | |
High-risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies. | |
Hydroa vacciniforme-like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites | |
In vitro radiosensitivity in a patient with dermatomyositis and cancer | |
Influence of ataxia telangiectasia gene dosage on bleomycin-induced chromosome breakage and inhibition of replication in human lymphoblastoid cell lines | |
Inhibition of mixed leukocyte culture reaction by 8-methoxypsoralen and long-wavelength ultraviolet radiation | |
Isotretinoin does prevent skin cancer. | |
Lessons learned from xeroderma pigmentosum. | |
Living with xeroderma pigmentosum: comprehensive photoprotection for highly photosensitive patients. | |
Managing the dysplastic naevus syndrome | |
Melanin acts as a potent UVB photosensitizer to cause an atypical mode of cell death in murine skin | |
Montagna Symposium 2011: 60th Anniversary--Advances in Science and Medicine Catalyzed by Pioneering Skin Research. | |
Mutational hotspot variability in an ultraviolet-treated shuttle vector plasmid propagated in xeroderma pigmentosum and normal human lymphoblasts and fibroblasts. | |
Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotype | |
N-methyl-N-nitrosourea-induced mutations in a shuttle plasmid replicated in human cells. | |
No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma | |
Normal vitamin D levels can be maintained despite rigorous photoprotection: six years' experience with xeroderma pigmentosum | |
A novel complex insertion/deletion mutation in the XPC DNA repair gene leads to skin cancer in an Iraqi family | |
NRAS hypermutability in familial melanoma with CDKN2A mutations--cause and effect? | |
Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literature | |
Pembrolizumab treatment of a patient with xeroderma pigmentosum with disseminated melanoma and multiple nonmelanoma skin cancers | |
Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 | |
Precursor naevi in cutaneous malignant melanoma: a proposed nomenclature | |
Psoralen plus ultraviolet radiation-induced inhibition of DNA synthesis and viability in human lymphoid cells in vitro | |
Rapid assessment of repair of ultraviolet DNA damage with a modified host-cell reactivation assay using a luciferase reporter gene and correlation with polymorphisms of DNA repair genes in normal human lymphocytes. | |
Rare diseases provide rare insights into DNA repair pathways, TFIIH, aging and cancer center | |
Recurrent scarring papulovesicular lesions on sun-exposed skin in a 22-year-old man. | |
Relationship of DNA strand breakage produced by bromodeoxyuridine to topoisomerase II activity in Bloom-syndrome fibroblasts | |
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. | |
Repair of UV photolesions in xeroderma pigmentosum group C cells induced by translational readthrough of premature termination codons. | |
Retinoid protection against x-ray-induced chromatid damage in human peripheral blood lymphocytes. | |
Semiautomated autoradiographic measurement of DNA repair in normal and xeroderma pigmentosum cultured human fibroblasts | |
Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2). | |
Structural and molecular hair abnormalities in trichothiodystrophy. | |
Survival of human lymphoblastoid cells after DNA damage measured by growth in microtiter wells | |
Thyroid nodules in xeroderma pigmentosum patients: a feature of premature aging | |
Transcriptional signatures of full-spectrum and non-UVB-spectrum solar irradiation in human skin. | |
Ultraviolet-induced mutations in Cockayne syndrome cells are primarily caused by cyclobutane dimer photoproducts while repair of other photoproducts is normal. | |
Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew. | |
UV-induced histone H2AX phosphorylation and DNA damage related proteins accumulate and persist in nucleotide excision repair-deficient XP-B cells | |
Xeroderma pigmentosum. A prototype disease of environmental-genetic interaction | |
Xeroderma pigmentosum and the role of UV-induced DNA damage in skin cancer. | |
Xeroderma pigmentosum--bridging a gap between clinic and laboratory. | |
Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities. | |
Xeroderma pigmentosum knockout mice: an immunologic tale | |
Xeroderma pigmentosum long-term lymphoid lines with increased ultraviolet sensitivity | |
XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients. |