Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 224,979,790 papers from all fields of science
Search
Sign In
Create Free Account
1p22.1
A chromosome band present on 1p
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
8 relations
ARHGAP29 wt Allele
BCAR3 wt Allele
BRDT wt Allele
Chromosome 1 Short Arm
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
mBAND and mFISH analysis of chromosomal aberrations and breakpoint distribution in chromosome 1 of AG01522 human fibroblasts that were exposed to radiation of different qualities.
F. Berardinelli
,
M. D. Vitis
,
+6 authors
A. Antoccia
Mutation Research. Genetic Toxicology and…
2015
Corpus ID: 37491081
2013
2013
Polymorphisms at Regions 1p22.1 (rs560426) and 8q24 (rs1530300) Are Risk Markers for Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population
Elizabete Bagordakis
,
Lívia-Ribeiro Paranaíba
,
+7 authors
R. Coletta
American Journal of Medical Genetics. Part A
2013
Corpus ID: 36970819
Polymorphisms at Regions 1p22.1 (rs560426) and 8q24 (rs1530300) Are Risk Markers for Nonsyndromic Cleft Lip and/or Palate in the…
Expand
2013
2013
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample
A. Böhmer
,
E. Mangold
,
+12 authors
K. Ludwig
American Journal of Medical Genetics. Part A
2013
Corpus ID: 5688662
Nonsyndromic cleft lip with or without cleft palate (NSCL/P), the most common type of orofacial clefting, is one of the most…
Expand
2003
2003
Age-Stratified QTL Genome Scan Analyses for Anthropometric Measures
S. Beck
,
W. M. Brown
,
A. Williams
,
J. Pierce
,
S. Rich
,
C. Langefeld
BMC Genetics
2003
Corpus ID: 11210093
With the availability of longitudinal data, age-specific (stratified) or age-adjusted genetic analyses have the potential to…
Expand
2000
2000
Nucleotide insertions and deletions within the homopolymeric runs of adenines and thymidines of BCL10 cDNAs in normal peripheral blood leukocytes.
Hidenobu Takahashi
,
Yumiko Maeda
,
Masao Seto
,
Yoshitaka Hosokawa
Blood
2000
Corpus ID: 42546752
The BCL10 gene was isolated from the breakpoint region of the t(1;14) in mucosa-associated lymphoid tissue (MALT) lymphomas,[1][1…
Expand
1998
1998
Structure and refinement of the physical mapping of the γ-glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant…
J. Rozet
,
S. Gerber
,
+7 authors
J. Kaplan
Cytogenetic and Genome Research
1998
Corpus ID: 46772373
Abstract. Glutathione is a ubiquitous antioxidant in mammalian tissues. The first step of its synthesis is catalyzed by the…
Expand
1990
1990
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic.
J. Kidd
,
Y. Matsubara
,
C. Castiglione
,
K. Tanaka
,
K. Kidd
Genomics
1990
Corpus ID: 2310215
1988
1988
The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1.
K. Kidd
,
J. Kidd
,
C. Castiglione
,
R. Sparkes
,
J. Egeland
,
E. Bakker
Human Heredity
1988
Corpus ID: 46835593
D1S2 was one of the first restriction fragment length polymorphisms (RFLPs) assigned to chromosome 1, but its regional location…
Expand
1987
1987
The Yt Blood Group System (ISBT No. 011)
M. Lewis
,
H. Kaita
,
+4 authors
J. Anderson
Vox Sanguinis
1987
Corpus ID: 28844595
Abstract. Allele frequencies of Yta (YT*1) and Ytb (YT*2) in a series of 659 random Canadian Caucasians are comparable to those…
Expand
1978
1978
Regional mapping on human genes for phosphoglucomutase-1 on chromosome 1 and beta-glucuronidase on chromosome 7 using mouse x human hybrids.
D. George
,
U. Francke
Human Heredity
1978
Corpus ID: 3313426
Two independent mouse-human somatic cell hybrid clones contained different, de novo chromosome rearrangements involving the short…
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