Literature DB >> 7979204

The International Collaborative Group on HNPCC.

H F Vasen1, J P Mecklin, P M Khan, H T Lynch.   

Abstract

The international collaborative group on HNPCC (ICG-HNPCC) was established in 1989. The original aims of the group were: (1) to develop minimal criteria for the identification of HNPCC, to provide a basis for uniformity in collaborative studies; (2) to improve patient and physician education about HNPCC; (3) to establish international collaborative studies, and (4) to promote the establishment of national (or regional) HNPCC registries. The administrative base of the group is attached to the Netherlands Foundation for the Detection of Hereditary Tumours at Leiden. The Netherlands. An International Informational Center on HNPCC was established at Creighton University in Omaha. The Hereditary Colon Cancer Newsletter (previously the Polyposis Newsletter) serves as a medium for communication about activities of the Group. At present, the Group has about 70 members from 23 countries, and its meetings are held annually. After a period of five years, it can be concluded that the objectives of the ICG-HNPCC have been successfully accomplished. The existence of the ICG-HNPCC has contributed to an increase in awareness of HNPCC among specialists throughout the world. Due to the rapid developments in molecular genetics in HNPCC, it seems very likely that HNPCC will be the first common hereditary cancer syndrome, which can be identified by simple blood DNA tests. The value of the ICG-HNPCC will be extremely important in finding a uniform answer to the question how to utilize DNA technology for the benefit of the human race.

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Mesh:

Year:  1994        PMID: 7979204

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  14 in total

1.  Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.

Authors:  Scott M Weissman; Randall Burt; James Church; Steve Erdman; Heather Hampel; Spring Holter; Kory Jasperson; Matt F Kalady; Joy Larsen Haidle; Henry T Lynch; Selvi Palaniappan; Paul E Wise; Leigha Senter
Journal:  J Genet Couns       Date:  2011-12-14       Impact factor: 2.537

Review 2.  Molecular basis for subdividing hereditary colon cancer?

Authors:  W M Grady
Journal:  Gut       Date:  2005-12       Impact factor: 23.059

3.  Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients.

Authors:  Francesc Balaguer; Judith Balmaña; Sergi Castellví-Bel; Ewout W Steyerberg; Montserrat Andreu; Xavier Llor; Rodrigo Jover; Sapna Syngal; Antoni Castells
Journal:  Gastroenterology       Date:  2007-10-26       Impact factor: 22.682

4.  Mismatch repair deficiency screening via immunohistochemical staining in young Asians with colorectal cancers.

Authors:  Min-Hoe Chew; Poh-Koon Koh; Melinda Tan; Kiat-Hon Lim; Loi Carol; Choong-Leong Tang
Journal:  World J Surg       Date:  2013-10       Impact factor: 3.352

5.  Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome.

Authors:  Julie Bouquier; Hélène Blons; Céline Narjoz; Fabrice Lécuru; Pierre Laurent-Puig; Anne-Sophie Bats
Journal:  Fam Cancer       Date:  2011-12       Impact factor: 2.375

6.  Microsatellite instability in gastric intestinal metaplasia in patients with and without gastric cancer.

Authors:  W K Leung; J J Kim; J G Kim; D Y Graham; A R Sepulveda
Journal:  Am J Pathol       Date:  2000-02       Impact factor: 4.307

Review 7.  Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management.

Authors:  Gregory Kouraklis; Evangelos P Misiakos
Journal:  Dig Dis Sci       Date:  2005-02       Impact factor: 3.199

8.  Genetic detection of Chinese hereditary nonpolyposis colorectal cancer.

Authors:  Long Cui; Hei-Ying Jin; Hui-Yu Cheng; Yu-Di Yan; Rong-Gui Meng; De-Hong Yu
Journal:  World J Gastroenterol       Date:  2004-01-15       Impact factor: 5.742

9.  First report of a de novo germline mutation in the MLH1 gene.

Authors:  Rein P Stulp; Yvonne J Vos; Bart Mol; Arend Karrenbeld; Monique de Raad; Huub J C van der Mijle; Rolf H Sijmons
Journal:  World J Gastroenterol       Date:  2006-02-07       Impact factor: 5.742

10.  Strategies for endometrial screening in the Lynch syndrome population: a patient acceptability study.

Authors:  K Elmasry; A J Davies; D G Evans; M N Seif; K Reynolds
Journal:  Fam Cancer       Date:  2009-06-13       Impact factor: 2.375

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