Literature DB >> 25872134

HNPCC-associated pheochromocytoma: expanding the tumor spectrum.

Brian P Riff1, Bryson W Katona, Myra Wilkerson, Katherine L Nathanson, David C Metz.   

Abstract

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Year:  2015        PMID： 25872134      PMCID： PMC4399001          DOI： 10.1097/MPA.0000000000000311

Source DB:  PubMed          Journal:  Pancreas        ISSN： 0885-3177            Impact factor:   3.327


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  6 in total

1.  Microsatellite instability and gene mutations in transforming growth factor-beta type II receptor are absent in small bowel carcinoid tumors.

Authors:  Mark Kidd; Geeta Eick; Michael D Shapiro; Robert L Camp; Shrikant M Mane; Irvin M Modlin
Journal:  Cancer       Date:  2005-01-15       Impact factor: 6.860

2.  Frequent promoter methylation of tumor-related genes in sporadic and men2-associated pheochromocytomas.

Authors:  R Dammann; U Schagdarsurengin; C Seidel; C Trümpler; C Hoang-Vu; O Gimm; H Dralle; G P Pfeifer; M Brauckhoff
Journal:  Exp Clin Endocrinol Diabetes       Date:  2005-01       Impact factor: 2.949

3.  Loss of expression of DNA mismatch repair proteins is rare in pancreatic and small intestinal neuroendocrine tumors.

Authors:  Thomas Arnason; Heidi L Sapp; Daniel Rayson; Penelope J Barnes; Magdalena Drewniak; Bassam A Nassar; Weei-Yuarn Huang
Journal:  Arch Pathol Lab Med       Date:  2011-12       Impact factor: 5.534

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

Authors:  Heather Hampel; Wendy L Frankel; Edward Martin; Mark Arnold; Karamjit Khanduja; Philip Kuebler; Hidewaki Nakagawa; Kaisa Sotamaa; Thomas W Prior; Judith Westman; Jenny Panescu; Dan Fix; Janet Lockman; Ilene Comeras; Albert de la Chapelle
Journal:  N Engl J Med       Date:  2005-05-05       Impact factor: 91.245

5.  MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

Authors:  H F Vasen; A Stormorken; F H Menko; F M Nagengast; J H Kleibeuker; G Griffioen; B G Taal; P Moller; J T Wijnen
Journal:  J Clin Oncol       Date:  2001-10-15       Impact factor: 44.544

6.  Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

Authors:  Marjolijn J L Ligtenberg; Roland P Kuiper; Tsun Leung Chan; Monique Goossens; Konnie M Hebeda; Marsha Voorendt; Tracy Y H Lee; Danielle Bodmer; Eveline Hoenselaar; Sandra J B Hendriks-Cornelissen; Wai Yin Tsui; Chi Kwan Kong; Han G Brunner; Ad Geurts van Kessel; Siu Tsan Yuen; J Han J M van Krieken; Suet Yi Leung; Nicoline Hoogerbrugge
Journal:  Nat Genet       Date:  2008-12-21       Impact factor: 38.330
  6 in total
  1 in total

1.  Adrenal pheochromocytoma in a patient with Lynch Syndrome.

Authors:  Katherine M Rodriguez; Kelly T Harris; Nirmish Singla
Journal:  Urol Case Rep       Date:  2022-02-03
  1 in total

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