Zobrazeno 1 - 10
of 62
pro vyhledávání: '"G J, Offerhaus"'
Autor:
E B, Conemans, G M, Raicu-Ionita, C R C, Pieterman, K M A, Dreijerink, O M, Dekkers, A R, Hermus, W W, de Herder, M L, Drent, A N A, van der Horst-Schrivers, B, Havekes, P H, Bisschop, G J, Offerhaus, I H M, Borel Rinkes, G D, Valk, H Th M, Timmers, M R, Vriens
Publikováno v:
Journal of endocrinological investigation. 41(6)
Pancreatic neuroendocrine tumors are a major manifestation of multiple endocrine neoplasia type 1 (MEN1). This tumor syndrome is caused by germline mutations in MEN1, encoding menin. Insight into pathogenesis of these tumors might lead to new biomark
Publikováno v:
Familial Cancer. 1:181-185
PARTIIPARTII Molecular andPhenotvvic Studies of Peutz-Jeshers Syndrome Chapte rr 7 Jann Peutz, Harold Jeghers and a remarkable combination of polyposis andd pigmentatio n of the skin and mucous membranes Josbertt J. Keller , G, Johan A, Offerhaus, Fr
Autor:
G J Offerhaus, Ralph H. Hruban, Wolter J. Mooi, Robbert J.C. Slebos, Otilia Dalesio, Sjoerd Rodenhuis
Publikováno v:
JNCI: Journal of the National Cancer Institute. 83:1024-1027
To investigate a possible relationship between the exposure to tobacco smoke and the presence of ras point mutations, we examined lung adenocarcinoma samples from 27 smokers and from 27 nonsmokers. Activating point mutations in K-ras (also known as K
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(7)
To provide an embryological explanation for the presence of ovarian stroma in cystadenomas of the liver and pancreas.Investigation of patients and embryos.From 1997 to 2001 in the Academic Medical Centre, Amsterdam, the Netherlands, nine women were t
Publikováno v:
Familial cancer. 1(3-4)
Autor:
J J, Keller, G J, Offerhaus, P, Drillenburg, E, Caspers, A, Musler, A, Ristimäki, F M, Giardiello
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(12)
Sulindac causes the reduction of adenomas in familial adenomatous polyposis (FAP) patients, but complete regression is unusual, and breakthrough of colorectal carcinoma during sulindac treatment has been described. The molecular features related to s
Autor:
A C, Tersmette, G M, Petersen, G J, Offerhaus, F C, Falatko, K A, Brune, M, Goggins, E, Rozenblum, R E, Wilentz, C J, Yeo, J L, Cameron, S E, Kern, R H, Hruban
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(3)
It has been estimated that familial aggregation and genetic susceptibility play a role in as many as 10% of patients with pancreatic cancer (PC). The quantified prospective risk of PC among first-degree relatives of PC patients has not been investiga
Autor:
J W, van Sandick, J J, van Lanschot, F J, ten Kate, G J, Offerhaus, P, Fockens, G N, Tytgat, H, Obertop
Publikováno v:
Cancer. 88(11)
As an alternative to surgical resection, endoscopic treatment modalities are being explored for the treatment of patients with early esophageal carcinoma. This study aimed to evaluate patterns of local growth and regional dissemination of early adeno
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(5)
Sebaceous gland carcinomas (SGCs) are rare malignant skin tumors occurring sporadically or as a phenotypic feature of the Muir-Torre syndrome (MTS). A subset of patients with MTS have a variant of the hereditary nonpolyposis colorectal cancer syndrom
Autor:
R E, Wilentz, M, Goggins, M, Redston, V A, Marcus, N V, Adsay, T A, Sohn, S S, Kadkol, C J, Yeo, M, Choti, M, Zahurak, K, Johnson, M, Tascilar, G J, Offerhaus, R H, Hruban, S E, Kern
Publikováno v:
The American journal of pathology. 156(5)
Medullary carcinomas of the pancreas are a recently described, histologically distinct subset of poorly differentiated adenocarcinomas that may have a unique pathogenesis and clinical course. To further evaluate these neoplasms, we studied genetic, p