H. Mehenni

发表

Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome

S. Antonarakis, B. Olsen, T. Krieg, 2001, Cytogenetic and Genome Research.

Peutz-Jeghers Syndrome: Confirmation of Linkage to Chromosome 19p1 3.3 and Identification of a Potential Second Locus, on 1 9q1 3.4

S. Antonarakis, A. Bermejo-Fenoll, Richards, 2006 .

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

U. C. Patel, J. Blouin, U. Radhakrishna, 1997, American journal of human genetics.

Abstracts of the 37th American Cytogenetics Conference

C. Steinlein, M. Schmid, S. Antonarakis, 2002, Cytogenetic and Genome Research.

An unexpected Cowden syndrome case found among members of a large familial adenomatous polyposis kindred.

P. Hutter, M. Nelen, M. Brundler, 2005, European journal of gastroenterology & hepatology.

LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.

A. Reymond, S. Antonarakis, D. Picard, 2005, Human molecular genetics.

Molecular and Clinical Characteristics in 46 Families Affected with Peutz–Jeghers Syndrome

M. Costanza, C. Rossier, R. Burt, 2007, Digestive Diseases and Sciences.

Cancer risks in LKB1 germline mutation carriers

M. Costanza, M. Miyaki, G. Guanti, 2006, Gut.

Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2

S. Antonarakis, U. Radhakrishna, K. Buchet-Poyau, 2002, Cytogenetic and Genome Research.

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.

N. Guex, S. Antonarakis, C. Rossier, 1998, American journal of human genetics.

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

S. Antonarakis, A. Bermejo-Fenoll, J. Blouin, 1997, American journal of human genetics.

The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.

J. Blouin, U. Radhakrishna, F. Sheth, 1997, American journal of medical genetics.