A. Gast

发表

TERT Promoter Mutations in Familial and Sporadic Melanoma

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2013, Science.

Highly Recurrent TERT Promoter Mutations in Human Melanoma

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2022 .

The SUMO E3 ligase RanBP2 promotes modification of the HDAC4 deacetylase

E. Miska, A. Dejean, S. Müller, 2002, The EMBO journal.

Opposed regulation of corepressor CtBP by SUMOylation and PDZ binding.

F. Melchior, Xin-Hua Feng, J. Hildebrand, 2003, Molecular cell.

B‐RAF mutations in tumors from melanoma‐breast cancer families

K. Hemminki, Rajiv Kumar, A. Försti, 2005, International journal of cancer.

ARLTS1 variants and melanoma risk

K. Hemminki, Rajiv Kumar, B. Burwinkel, 2006, International journal of cancer.

B-RAF and N-RAS Mutations Are Preserved during Short Time In Vitro Propagation and Differentially Impact Prognosis

D. Schadendorf, J. Becker, S. Ugurel, 2007, PloS one.

Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.

E. Papaemmanuil, J. Vijayakrishnan, R. Houlston, 2010, Blood.

lymphoblastic leukemia genetic polymorphisms and susceptibility to childhood acute MTHFR

D. Labuda, Rajiv Kumar, B. Burwinkel, 2011 .

MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia.

K. Hemminki, Rajiv Kumar, B. Burwinkel, 2005, Blood.

Association of Inherited Variation in Toll-Like Receptor Genes with Malignant Melanoma Susceptibility and Survival

D. Schadendorf, C. Plass, K. Hemminki, 2011, PloS one.

N-terminal sequences of the human androgen receptor in DNA binding and transrepressing functions

A. Gast, J. Schneikert, A. Cato, 1998, The Journal of Steroid Biochemistry and Molecular Biology.

ARLTS1 polymorphisms and basal cell carcinoma of the skin

K. Hemminki, Rajiv Kumar, P. Rudnai, 2007, Hereditary cancer in clinical practice.

ARLTS 1 polymorphisms and basal cell carcinoma of the skin

K. Hemminki, Rajiv Kumar, P. Rudnai, 2007 .

Multiple melanomas after treatment for Hodgkin lymphoma in a non-Dutch p16-Leiden mutation carrier with 2 MC1R high-risk variants.

D. Schadendorf, S. Ugurel, K. Hemminki, 2006, Archives of dermatology.

Epigenetic deregulation of TCF21 inhibits metastasis suppressor KISS1 in metastatic melanoma.

Dirk Schadendorf, Thomas Hielscher, Dieter Weichenhan, 2011, Carcinogenesis.

Brief report Veriﬁcation of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood

E. Papaemmanuil, M. Greaves, J. Vijayakrishnan, 2010 .

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk

James Allan, E. Papaemmanuil, J. Vijayakrishnan, 2010, Nature Genetics.

A distinct modulating domain in glucocorticoid receptor monomers in the repression of activity of the transcription factor AP‐1.

P. Herrlich, H. Rahmsdorf, S. Heck, 1994, The EMBO journal.

Somatic alterations in the melanoma genome: A high‐resolution array‐based comparative genomic hybridization study

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2010, Genes, chromosomes & cancer.

The Nucleoporin RanBP2 Has SUMO1 E3 Ligase Activity

A. Dejean, F. Melchior, J. Seeler, 2002, Cell.

Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma.

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2010, Mutation research.

A case–control study of childhood acute lymphoblastic leukaemia and polymorphisms in the TGF‐β and receptor genes

K. Hemminki, Rajiv Kumar, M. Schrappe, 2009, Pediatric blood & cancer.

Activation of two mutant androgen receptors from human prostatic carcinoma by adrenal androgens and metabolic derivatives of testosterone.

H. Klocker, G. Bartsch, A. Gast, 1996, Cancer detection and prevention.

Differential gene expression in melanocytic nevi with the V600E BRAF mutation

R. Wellenreuther, K. Hemminki, Rajiv Kumar, 2007, Genes, chromosomes & cancer.

Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case–control study

K. Hemminki, Rajiv Kumar, B. Burwinkel, 2007, Leukemia.

Increases in Adult Life Expectancy in Rural South Africa : Valuing the Scale-Up of HIV Treatment

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2022 .

Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2009, Cancer Immunology, Immunotherapy.

Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients.

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2009, Mutation research.

Integrin genes and susceptibility to human melanoma.

D. Schadendorf, K. Hemminki, Rajiv Kumar, 2012, Mutagenesis.

CAG-repeat expansion in androgen receptor in Kennedy's disease is not a loss of function mutation

H. Klocker, G. Bartsch, G. Ransmayr, 1996, Molecular and Cellular Endocrinology.

A single amino acid exchange abolishes dimerization of the androgen receptor and causes Reifenstein syndrome

H. Klocker, A. Gast, A. Cato, 1995, Molecular and Cellular Endocrinology.

Association between the B-RAF/N-RAS mutations, the CDKN2A alterations and the MC1R variants in melanoma

D. Schadendorf, S. Ugurel, K. Hemminki, 2006 .