Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 234,325,640 papers from all fields of science
Search
Sign In
Create Free Account
APC gene
Known as:
Genes, APC
, DP2
, adenomatous polyposis coli
Expand
Tumor suppressor genes located in the 5q21 region on the long arm of human chromosome 5. The mutation of these genes is associated with familial…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
49 relations
APC Gene Mut Anal Bld/T
APC protein, human
Adenocarcinoma of rectum
Adenocarcinoma of the large intestine
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
A genome screen of families at high risk for Hodgkin lymphoma: evidence for a susceptibility gene on chromosome 4
L. Goldin
,
M. McMaster
,
+4 authors
M. Tucker
Journal of Medical Genetics
2005
Corpus ID: 31646356
Hodgkin’s disease was recently designated Hodgkin lymphoma (HL) in the World Health Organization Classification.1 The National…
Expand
2004
2004
Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?
C. Marcelis
,
H. W. van der Putten
,
C. Tops
,
L. Lutgens
,
U. Moog
Familial Cancer
2004
Corpus ID: 20772306
Hereditary Non-Polyposis Colorectal Cancer (HNPCC, Lynch syndrome) is an autosomal dominant condition of cancer susceptibility…
Expand
Review
1994
Review
1994
Silent Adrenal Nodules in von Hippel-Lindau Disease Suggest Pheochromocytoma
B. Aprill
,
A. Drake
,
D. Lasseter
,
K. M. Mohamed Shakir
Annals of Internal Medicine
1994
Corpus ID: 32771566
Von Hippel-Lindau disease is an autosomal-dominant disorder characterized by retinal angiomatosis, cerebellar hemangioblastoma…
Expand
Highly Cited
1993
Highly Cited
1993
Loss of heterozygosity in familial breast carcinomas.
Annika Lindblom
,
Lambert Skoog
,
Sam Rotstein
,
B. Werelius
,
C. Larsson
,
M. Nordenskjöld
Cancer Research
1993
Corpus ID: 20839353
Three loci have been implicated in the etiology of familial breast cancer; the BRCA1 locus on 17q, the p53 gene on 17p, and the…
Expand
1991
1991
Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.
F. Giardiello
,
G. Offerhaus
,
+6 authors
S. R. Hamilton
Gut
1991
Corpus ID: 36098873
Familial adenomatous polyposis is an autosomal dominant disease characterised by the development of hundreds of colorectal…
Expand
1987
1987
Binding of monoclonal antibody (4F2) to its cell surface antigen on dispersed adenomatous parathyroid cells raises cytosolic calcium and inhibits parathyroid hormone secretion.
J. Posillico
,
S. Srikanta
,
G. Eisenbarth
,
V. Quaranta
,
S. Kajiji
,
E. Brown
Journal of Clinical Endocrinology and Metabolism
1987
Corpus ID: 44370852
In the course of characterizing monoclonal antibodies (MAbs) recognizing cell surface antigens on dispersed human parathyroid…
Expand
1986
1986
Analyses of prealbumin mRNAs in individuals with familial amyloidotic polyneuropathy.
S. Mita
,
S. Maeda
,
K. Shimada
,
S. Araki
Journal of Biochemistry (Tokyo)
1986
Corpus ID: 28440196
The distribution of prealbumin mRNA in various tissues of a control subject and an individual with familial amyloidotic…
Expand
Highly Cited
1982
Highly Cited
1982
A familial hemorrhagic diathesis in a Dutch family: an inherited deficiency of alpha 2-antiplasmin.
C. Kluft
,
E. Vellenga
,
E. Brommer
,
G. Wijngaards
Blood
1982
Corpus ID: 21029465
This study concerns a case of congenital homozygous deficiency in alpha 2-antiplasmin associated with a severe hemorrhagic…
Expand
1978
1978
Plasma hormone profiles of young women at risk for familial breast cancer.
J. Fishman
,
D. Fukushima
,
+5 authors
K. Maloney
Cancer Research
1978
Corpus ID: 40054251
The plasma hormone concentrations of 30 young women, who were judged by genetic analysis to be at high risk for familial breast…
Expand
1965
1965
FAMILIAL SUPRAVALVAR AORTIC STENOSIS
W. F. Logan
,
E. Jones
,
E. Walker
,
N. Coulshed
,
E. J. Epstein
,
Walker Coulshed Jones
British heart journal
1965
Corpus ID: 27674086
Though supravalvar aortic stenosis is uncommon and fewer than 80 cases have been described, nevertheless, a clinical picture is…
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