Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 238,226,766 papers from all fields of science
Search
Sign In
Create Free Account
1q23
A chromosome band present on 1q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
12 relations
Chromosomes
F5 Leiden Allele
F5 wt Allele
FASLG wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Expression Profiling of FasL Gene in Human Blood Tissues and its Correlation with Severe Acute Pancreatitis (SAP)
Saurav Biswas
,
M. Singh
International Journal of Life-Sciences Scientific…
2018
Corpus ID: 92359646
Blood leukocytes have a vital role in easing general inflammation through acute pancreatitis. Irrespective of topical growths in…
Expand
2014
2014
Exploring novel system biology approaches to understand the molecular mechanisms of immune responses
C. Garbutt
2014
Corpus ID: 83330200
2013
2013
A NOVEL LMNA MUTATION IN TWO SOUTH INDIAN SIBLINGS WITH HUTCHINSON-GILFORD PROGERIA SYNDROME
A. Munshi
,
U. Satyanarayana
,
+5 authors
A. Jyothy
2013
Corpus ID: 76381041
Hutchinson-Gilford progeria syndrome (HGPS: MIM 176670), first described over a century ago, is an extremely rare genetic…
Expand
2009
2009
Genome-wide association study to search for SNPs affecting gene expression in a general population
D. Mehta
2009
Corpus ID: 91170626
The aim of this study was to identify SNPs affecting gene expression in the general population. To achieve this, a genome-wide…
Expand
2005
2005
Gly392Cys missense mutation in the A2 domain of factor V causing severe factor V deficiency: molecular characterization by expression of the recombinant protein
Tsai-Yun Chen
,
Tsun-Mei Lin
,
Hsiao-Yen Chen
,
Chiy-Lin Wu
,
C. Tsao
Thrombosis and Haemostasis
2005
Corpus ID: 4979502
Gly392Cys missense mutation in the A2 domain of factor V causing severe factor V deficiency: molecular characterization by…
Expand
2004
2004
TO JMG A novel mutation in the ATP 1 A 2 gene causes alternating hemiplegia of childhood
M. Bassi
,
N. Bresolin
,
+9 authors
G. Casari
2004
Corpus ID: 6740792
A lternating hemiplegia of childhood (AHC, MIM 104290) is a rare syndrome, characterised by early onset of episodic hemior…
Expand
2003
2003
Identification of a novel candidate gene PBX1 within the putative systemic lupus erythematosus susceptibility locus at 1q23-24 in a Chinese cohort
Shun Chen
2003
Corpus ID: 87361184
Objective To identify candidate genes within the putative systemic lupus erythematosus (SLE) susceptibility locus at 1q23 24…
Expand
1997
1997
Human Gene Mapping Report: Proteinase inhibitor 8 Map position 18q21.3
Fiona L. Scott
,
H. Eyre
,
Lisa M. Ooms
,
Jiu-Ru Sun
,
Phillip I. Bird
,
Grant R. Sutherland
Chromosome Research
1997
Corpus ID: 33038560
Functional T-cell antigen receptors are diverse structures in obligate association with CD3 proteins and the zeta chain protein…
Expand
1984
1984
[Is there a functional equivalence between abnormalities of the long arm of chromosome 1 and the presence of Epstein-Barr virus in continuous lines of Burkitt's lymphoma?].
R. Berger
,
A. Bernheim
Comptes rendus de l'Academie des sciences. Serie…
1984
Corpus ID: 19669838
Chromosome 1 long arm abnormalities (translocations, partial of complete trisomies) are non-randomly but inconstantly associated…
Expand
1982
1982
Cytogenetic studies on four cases of non-endemic Burkitt lymphoma.
R. Slater
,
H. Behrendt
,
P. van Heerde
Medical and Pediatric Oncology
1982
Corpus ID: 39889819
Cytogenetic studies carried out on four children with non-endemic Burkitt lymphoma showed: 1) Two with the typical translocation…
Expand