M. Stark

发表

Identification of novel aberrant methylation of BASP1 and SRD5A2 for early diagnosis of hepatocellular carcinoma by genome-wide search.

Yoshihiko Hamamoto, Toshiaki Miura, Markus Stark, 2008, International journal of oncology.

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.

D E Goldgar, M. Papotti, F. Canzian, 2001, American journal of human genetics.

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

F. Canzian, M. Schlumberger, D. Goldgar, 1999, The Journal of clinical endocrinology and metabolism.

A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene

W. Krone, G. Assum, M. Stark, 1991, Human Genetics.

EVI2B, a gene lying in an intron of the neurofibromatosis type 1 (NF1) gene, is as the NF1 gene involved in differentiation of melanocytes and keratinocytes and is overexpressed in cells derived from NF1 neurofibromas.

D. Kaufmann, S. Hoffmeyer, J. Griesser, 1999, DNA and cell biology.

A new candidate region for the positional cloning of the XLP gene

Jack R. Davis, A. Coffey, G. Lenoir, 1998, European Journal of Human Genetics.

Single-cell PCR performed with neurofibroma Schwann cells reveals the presence of both alleles of the neurofibromatosis type 1 (NF1) gene

W. Krone, G. Assum, M. Stark, 1995, Human Genetics.

Analysis of segregation and expression of an identified mutation at the neuroflbromatosis type 1 locus

W. Krone, G. Assum, D. Kaufmann, 1992, Human Genetics.

Elevated levels of circulating cell-free DNA in the blood of patients with hepatitis C virus-associated hepatocellular carcinoma.

N. Iizuka, M. Oka, T. Tamesa, 2006, Anticancer research.

Investigations of neurofibromin expression in the skin of patients with NF 1 (neurofibromatosis type 1)

I. Eisenbarth, W. Krone, G. Assum, 1994 .

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.

M. Stratton, G. Bignell, W. Foulkes, 1997, American journal of human genetics.

At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family.

F. Canzian, F. Lesueur, G. Romeo, 1999, European journal of endocrinology.