Mehenni H - Search Results

1

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

Mehenni H, Lin-Marq N, Buchet-Poyau K, Reymond A, Collart MA, Picard D, Antonarakis SE. Mehenni H, et al. Hum Mol Genet. 2005 Aug 1;14(15):2209-19. doi: 10.1093/hmg/ddi225. Epub 2005 Jun 29. Hum Mol Genet. 2005. PMID: 15987703

2

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

Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, Guex N, Blouin JL, Scott HS, Antonarakis SE. Mehenni H, et al. Am J Hum Genet. 1998 Dec;63(6):1641-50. doi: 10.1086/302159. Am J Hum Genet. 1998. PMID: 9837816 Free PMC article.

3

Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.

Mehenni H, Resta N, Guanti G, Mota-Vieira L, Lerner A, Peyman M, Chong KA, Aissa L, Ince A, Cosme A, Costanza MC, Rossier C, Radhakrishna U, Burt RW, Picard D. Mehenni H, et al. Dig Dis Sci. 2007 Aug;52(8):1924-33. doi: 10.1007/s10620-006-9435-3. Epub 2007 Apr 3. Dig Dis Sci. 2007. PMID: 17404884

4

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

Mehenni H, Blouin JL, Radhakrishna U, Bhardwaj SS, Bhardwaj K, Dixit VB, Richards KF, Bermejo-Fenoll A, Leal AS, Raval RC, Antonarakis SE. Mehenni H, et al. Am J Hum Genet. 1997 Dec;61(6):1327-34. doi: 10.1086/301644. Am J Hum Genet. 1997. PMID: 9399902 Free PMC article.

5

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.

Buchet-Poyau K, Mehenni H, Radhakrishna U, Antonarakis SE. Buchet-Poyau K, et al. Among authors: mehenni h. Cytogenet Genome Res. 2002;97(3-4):171-8. doi: 10.1159/000066620. Cytogenet Genome Res. 2002. PMID: 12438709

6

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

Radhakrishna U, Blouin JL, Mehenni H, Patel UC, Patel MN, Solanki JV, Antonarakis SE. Radhakrishna U, et al. Among authors: mehenni h. Am J Hum Genet. 1997 Mar;60(3):597-604. Am J Hum Genet. 1997. PMID: 9042919 Free PMC article.

7

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.

Marneros AG, Mehenni H, Reichenberger E, Antonarakis SE, Krieg T, Olsen BR. Marneros AG, et al. Among authors: mehenni h. Cytogenet Cell Genet. 2001;92(3-4):213-6. doi: 10.1159/000056905. Cytogenet Cell Genet. 2001. PMID: 11435690

8

Cancer risks in LKB1 germline mutation carriers.

Mehenni H, Resta N, Park JG, Miyaki M, Guanti G, Costanza MC. Mehenni H, et al. Gut. 2006 Jul;55(7):984-90. doi: 10.1136/gut.2005.082990. Epub 2006 Jan 11. Gut. 2006. PMID: 16407375 Free PMC article.

9

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

Radhakrishna U, Blouin JL, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE. Radhakrishna U, et al. Among authors: mehenni h. Am J Med Genet. 1997 Jul 11;71(1):80-6. doi: 10.1002/(sici)1096-8628(19970711)71:1<80::aid-ajmg15>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9215774

10

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

Mehenni H, Friedl W, Nelen MR, Hutter P, Brundler MA. Mehenni H, et al. Eur J Gastroenterol Hepatol. 2005 Dec;17(12):1407-12. doi: 10.1097/01.meg.0000184983.38398.b6. Eur J Gastroenterol Hepatol. 2005. PMID: 16292097

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