Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,317,621 papers from all fields of science
Search
Sign In
Create Free Account
DSG2 gene
Known as:
DESMOGLEIN 2
, DSG2
, CDHF5
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
desmoglein 2
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Therapeutic and prophylactic gastrectomy in a family with hereditary diffuse gastric cancer secondary to a CDH1 mutation: a case series
O. Gjyshi
,
P. Vashi
,
+5 authors
H. Halabi
World Journal of Surgical Oncology
2018
Corpus ID: 51626898
BackgroundGastric cancer is the fifth most prevalent and the third most lethal cancer worldwide, causing approximately 720,000…
Expand
2014
2014
Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome
Valeria Molinaro
,
V. Pensotti
,
+8 authors
G. Ranzani
Genes, Chromosomes and Cancer
2014
Corpus ID: 20950013
Germline inactivation of the E‐cadherin gene (CDH1) is associated with hereditary diffuse gastric cancer (HDGC), a rare autosomal…
Expand
2014
2014
Presymptomatic Identification of CDH1 Germline Mutation in a Healthy Korean Individual with Family History of Gastric Cancer
H. Choi
,
C. Ki
,
S. Suh
,
Jong-Won Kim
Annals of Laboratory Medicine
2014
Corpus ID: 19150924
Gastric cancer (GC) is one of the most common cancers with high morbidity and mortality. Familial GC is seen in 10% of cases, and…
Expand
2011
2011
ADP-Ribosylation Factor 6 Mediates E-Cadherin Recovery by Chemical Chaperones
J. Figueiredo
,
J. Simões-Correia
,
O. Söderberg
,
G. Suriano
,
R. Seruca
PLoS ONE
2011
Corpus ID: 248833
E-cadherin plays a powerful tumor suppressor role. Germline E-cadherin mutations justify 30% of Hereditary Diffuse Gastric Cancer…
Expand
2010
2010
Germline mutation of the E-cadherin gene in three sibling cases with advanced gastric cancer: clinical consequences for the other family members
B. Mayrbaeurl
,
G. Keller
,
+7 authors
J. Thaler
European Journal of Gastroenterology and…
2010
Corpus ID: 29171333
Background and aims Germline mutations in the E-cadherin (CDH1) gene have been found in families with hereditary diffuse gastric…
Expand
Review
2010
Review
2010
Arrhythmogenic right ventricular cardiomyopathy is a disease of cardiac stem cells
R. Lombardi
,
A. Marian
Current Opinion in Cardiology
2010
Corpus ID: 13543863
Purpose To review recent developments in clinical aspects, molecular genetics and pathogenesis of arrhythmogenic right…
Expand
2010
2010
A novel truncating mutation in the E-cadherin gene in the first Iranian family with hereditary diffuse gastric cancer.
Saeed Reza Ghaffari
,
M. Rafati
,
T. Sabokbar
,
J. Dastan
European Journal of Surgical Oncology
2010
Corpus ID: 11391344
Review
2008
Review
2008
Hereditary diffuse gastric cancer: prophylactic surgical oncology implications.
H. Lynch
,
Edibaldo Silva
,
D. Wirtzfeld
,
P. Hebbard
,
J. Lynch
,
D. Huntsman
Surgical Clinics of North America
2008
Corpus ID: 45857012
2000
2000
The amino- and carboxyl-terminal tails of (beta)-catenin reduce its affinity for desmoglein 2.
James K. Wahl
,
J. E. Nieset
,
P. Sacco-Bubulya
,
Tammy M. Sadler
,
Keith R. Johnson
,
M. Wheelock
Journal of Cell Science
2000
Corpus ID: 20745450
beta-catenin and plakoglobin are members of the armadillo family of proteins and were first identified as components of…
Expand
2000
2000
Expression of a single pair of desmosomal glycoproteins renders the corneal epithelium unique amongst stratified epithelia.
A. Messent
,
M. Blissett
,
+5 authors
M. Boulton
Investigative Ophthalmology and Visual Science
2000
Corpus ID: 12063564
PURPOSE To determine desmosomal glycoprotein isoform expression in bovine corneal, limbal, and conjunctival epithelium and…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE