Hampel H - Search Results

1

Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis.

Haraldsdottir S, Roth R, Pearlman R, Hampel H, Arnold CA, Frankel WL. Haraldsdottir S, et al. Among authors: hampel h. Fam Cancer. 2016 Apr;15(2):253-60. doi: 10.1007/s10689-015-9856-2. Fam Cancer. 2016. PMID: 26666765

2

Gene expression in papillary thyroid carcinoma reveals highly consistent profiles.

Huang Y, Prasad M, Lemon WJ, Hampel H, Wright FA, Kornacker K, LiVolsi V, Frankel W, Kloos RT, Eng C, Pellegata NS, de la Chapelle A. Huang Y, et al. Among authors: hampel h. Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15044-9. doi: 10.1073/pnas.251547398. Proc Natl Acad Sci U S A. 2001. PMID: 11752453 Free PMC article.

3

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.

Nakagawa H, Yan H, Lockman J, Hampel H, Kinzler KW, Vogelstein B, De La Chapelle A. Nakagawa H, et al. Among authors: hampel h. Cancer Res. 2002 Aug 15;62(16):4579-82. Cancer Res. 2002. PMID: 12183410

4

Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.

Pyatt RE, Nakagawa H, Hampel H, Sedra M, Fuchik MB, Comeras I, de la Chapelle A, Prior TW. Pyatt RE, et al. Among authors: hampel h. Clin Genet. 2003 Mar;63(3):215-8. doi: 10.1034/j.1399-0004.2003.00040.x. Clin Genet. 2003. PMID: 12694232

5

Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques.

Nakagawa H, Hampel H, de la Chapelle A. Nakagawa H, et al. Among authors: hampel h. Hum Mutat. 2003 Sep;22(3):258. doi: 10.1002/humu.9171. Hum Mutat. 2003. PMID: 12938096

6

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation.

Nakagawa H, Lockman JC, Frankel WL, Hampel H, Steenblock K, Burgart LJ, Thibodeau SN, de la Chapelle A. Nakagawa H, et al. Among authors: hampel h. Cancer Res. 2004 Jul 15;64(14):4721-7. doi: 10.1158/0008-5472.CAN-03-2879. Cancer Res. 2004. PMID: 15256438

7

MSH6 missense mutations are often associated with no or low cancer susceptibility.

Kariola R, Hampel H, Frankel WL, Raevaara TE, de la Chapelle A, Nyström-Lahti M. Kariola R, et al. Among authors: hampel h. Br J Cancer. 2004 Oct 4;91(7):1287-92. doi: 10.1038/sj.bjc.6602129. Br J Cancer. 2004. PMID: 15354210 Free PMC article.

8

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Hampel H, et al. N Engl J Med. 2005 May 5;352(18):1851-60. doi: 10.1056/NEJMoa043146. N Engl J Med. 2005. PMID: 15872200 Free article.

9

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

Hampel H, Stephens JA, Pukkala E, Sankila R, Aaltonen LA, Mecklin JP, de la Chapelle A. Hampel H, et al. Gastroenterology. 2005 Aug;129(2):415-21. doi: 10.1016/j.gastro.2005.05.011. Gastroenterology. 2005. PMID: 16083698

10

Somatic acquisition and signaling of TGFBR1*6A in cancer.

Pasche B, Knobloch TJ, Bian Y, Liu J, Phukan S, Rosman D, Kaklamani V, Baddi L, Siddiqui FS, Frankel W, Prior TW, Schuller DE, Agrawal A, Lang J, Dolan ME, Vokes EE, Lane WS, Huang CC, Caldes T, Di Cristofano A, Hampel H, Nilsson I, von Heijne G, Fodde R, Murty VV, de la Chapelle A, Weghorst CM. Pasche B, et al. Among authors: hampel h. JAMA. 2005 Oct 5;294(13):1634-46. doi: 10.1001/jama.294.13.1634. JAMA. 2005. PMID: 16204663

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