Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 234,145,379 papers from all fields of science
Search
Sign In
Create Free Account
17q25
A chromosome band present on 17q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
13 relations
17q
ASPSCR1 wt Allele
BAIAP2 wt Allele
BIRC5 wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Inherited focal, episodic neuropathies
P. Chance
Neuromolecular medicine
2006
Corpus ID: 43877600
Hereditary neuropathy with liability to pressure palsies (HNPP; also called tomaculous neuropathy) is an autosomal-dominant…
Expand
2006
2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q
C. Pang
,
B. Fan
,
+7 authors
R. Ritch
2006
Corpus ID: 45051917
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle…
Expand
Review
2004
Review
2004
Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites
J. Huret
,
J. Tanzer
,
M. Henry-Amar
Human Genetics
2004
Corpus ID: 7049051
SummaryThree hundred and twenty-five aberrant breakpoints in chronic myelogenous leukaemia (CML) with Philadelphia chromosome…
Expand
Review
2003
Review
2003
Genome-wide characterization of genetic aberrations in pancreatic cancer
E. Mahlamäki
2003
Corpus ID: 53334936
12 INTRODUCTION 14 REVIEW OF THE LITERATURE 16 1. Pathology of pancreatic cancer 16 2. Epidemiology of pancreatic cancer 18 3…
Expand
2002
2002
Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q
M. Hitchins
,
S. Abu-Amero
,
+4 authors
G. Moore
Journal of Medical Genetics
2002
Corpus ID: 33911476
Silver-Russell syndrome (SRS) (MIM 180860) is characterised by intrauterine and postnatal growth restriction, in association with…
Expand
2002
2002
Investigation of the GRB 2 , GRB 7 , and CSH 1 genes as candidates for the Silver-Russell syndrome ( SRS ) on chromosome 17 q
M. Hitchins
,
S. Abu-Amero
,
+4 authors
G. Moore
2002
Corpus ID: 45826603
Silver-Russell syndrome (SRS) (MIM 180860) is characterised by intrauterine and postnatal growth restriction, in association with…
Expand
2001
2001
Epidermodysplasia Verruciformis Defines a Subset of Cutaneous Human Papillomaviruses
G. Orth
,
M. Fãvre
,
S. Majewski
,
S. Jabłońska
Journal of Virology
2001
Corpus ID: 8702402
In a very interesting and provocative article, Antonsson et al. reported a high prevalence of known or as-yet-uncharacterized…
Expand
1997
1997
SHORT COMMUNICATION Molecular Characterization and Localization of the Human MAFG Gene
V. Blank
,
J. Knoll
,
N. Andrews
1997
Corpus ID: 10354399
The human MAFG gene encodes a basic-leucine zip- p45 NF-E2 and suggest that the p45/MAFG heteroper (bZIP) protein that belongs to…
Expand
1995
1995
The gene (LGALS3BP) encoding the serum protein 90K, associated with cancer and infection by the human immunodeficiency virus, maps at 17q25.
G. Calabrese
,
I. Sures
,
F. Pompetti
,
G. Natoli
,
G. Palka
,
S. lacobelli
Cytogenetics and Cell Genetics
1995
Corpus ID: 46880872
Levels of a 90-kDa tumor associated protein, designated 90K (gene symbol LGALS3BP), have been found elevated in the serum of…
Expand
1989
1989
Evolution of multiple cytogenetic clones and leukemic transformation in a case of myelodysplastic syndrome
E. Donti
,
G. V. Donti
,
F. Falzetti
,
A. Rosetti
,
F. Grignani
,
A. Tabilio
Medical Oncology and Tumor Pharmacotherapy
1989
Corpus ID: 36749800
The cytogenetic follow-up of a case of refractory anemia with excess of blasts (RAEB) that rapidly evolved to acute myeloblastic…
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