Sunlight and skin cancer: Another link revealed

Por Kraemer, Kenneth H.
Publicado em 1997

Do not underestimate nucleotide excision repair: It not only predicts melanoma risk but also survival outcome

Por Emmert, Steffen, Kraemer, Kenneth H.
Publicado em 2013

SHINING A LIGHT ON XERODERMA PIGMENTOSUM

Por DiGiovanna, John J., Kraemer, Kenneth H.
Publicado em 2012

Forty Years of Research on Xeroderma Pigmentosum at the US National Institutes of Health()

Por Kraemer, Kenneth H., DiGiovanna, John J.
Publicado no Photochem Photobiol (2015)

Founder Mutations in Xeroderma Pigmentosum

Por Tamura, Deborah, DiGiovanna, John J., Kraemer, Kenneth H.
Publicado em 2010

The xeroderma pigmentosum group C gene leads to selective repair of cyclobutane pyrimidine dimers rather than 6-4 photoproducts

Por Emmert, Steffen, Kobayashi, Nobuhiko, Khan, Sikandar G., Kraemer, Kenneth H.
Publicado em 2000

The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms

Por Emmert, Steffen, Schneider, Thomas D., Khan, Sikandar G., Kraemer, Kenneth H.
Publicado em 2001

Xeroderma pigmentosum and other diseases of human premature aging and DNA repair: Molecules to patients

Por Niedernhofer, Laura J., Bohr, Vilhelm A., Sander, Miriam, Kraemer, Kenneth H.
Publicado em 2011

Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients

Por Ueda, Takahiro, Compe, Emmanuel, Catez, Philippe, Kraemer, Kenneth H., Egly, Jean-Marc
Publicado em 2009

UV-induced histone H2AX phosphorylation and DNA damage related proteins accumulate and persist in nucleotide excision repair-deficient XP-B cells

Por Oh, Kyu-Seon, Bustin, Michael, Mazur, Sharlyn J., Appella, Ettore, Kraemer, Kenneth H.
Publicado em 2010

Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damage

Por Oh, Kyu-Seon, Imoto, Kyoko, Boyle, Jennifer, Khan, Sikandar G., Kraemer, Kenneth H.
Publicado em 2007

Multiple Skin Cancers in Adults with Mutations in the XP-E (DDB2) DNA Repair Gene

Por Oh, Kyu-Seon, Emmert, Steffen, Tamura, Deborah, DiGiovanna, John J., Kraemer, Kenneth H.
Publicado em 2010

Repair of UV photolesions in xeroderma pigmentosum group C cells induced by translational readthrough of premature termination codons

Por Kuschal, Christiane, DiGiovanna, John. J., Khan, Sikandar G., Gatti, Richard A., Kraemer, Kenneth H.
Publicado em 2013

Nucleotide Excision Repair Proteins Rapidly Accumulate but Fail to Persist in Human XP-E (DDB2 Mutant) Cells

Por Oh, Kyu-Seon, Imoto, Kyoko, Emmert, Steffen, Tamura, Deborah, DiGiovanna, John J., Kraemer, Kenneth. H.
Publicado em 2011

Growth and Nutrition in Children with Trichothiodystrophy

Por Atkinson, Emily C., Thiara, Diana, Tamura, Deborah, DiGiovanna, John J., Kraemer, Kenneth H., Hadigan, Colleen
Publicado em 2014

Melanin acts as a potent UVB photosensitizer to cause an atypical mode of cell death in murine skin

Por Takeuchi, Seiji, Zhang, Wengeng, Wakamatsu, Kazumasa, Ito, Shosuke, Hearing, Vincent J., Kraemer, Kenneth H., Brash, Douglas E.
Publicado em 2004

XERODERMA PIGMENTOSUM, TRICHOTHIODYSTROPHY AND COCKAYNE SYNDROME: A COMPLEX GENOTYPE-PHENOTYPE RELATIONSHIP

Por Kraemer, Kenneth H., Patronas, Nicholas J., Schiffmann, Raphael, Brooks, Brian P., Tamura, Deborah, DiGiovanna, John J.
Publicado em 2007

Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotype

Por Heller, Elizabeth R., Khan, Sikandar G., Kuschal, Christiane, Tamura, Deborah, DiGiovanna, John J., Kraemer, Kenneth H.
Publicado no J Invest Dermatol (2014)

Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities

Por Moriwaki, Shinichi, Takigawa, Masahiro, Igarashi, Naoya, Nagai, Yayoi, Amano, Hiroo, Ishikawa, Osamu, Khan, Sikandar G., Kraemer, Kenneth H.
Publicado em 2012

Montagna Symposium 2011: 60th Anniversary—Advances in Science and Medicine Catalyzed By Pioneering Skin Research

Por Yuspa, Stuart H., Kraemer, Kenneth H., Dlugosz, Andrzej A., Roop, Dennis R., Kulesz-Martin, Molly, Bickenbach, Jackie R.
Publicado em 2012