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12p13.2
A chromosome band present on 12p
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosome 12 Short Arm
Chromosomes
TNFRSF1A wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
12p deletion spectrum syndrome: a new case report reinforces the evidence regarding the potential relationship to autism spectrum disorder and related developmental impairments
M. Leyser
,
Bruno Leonardo Dias
,
Ana Luiza Coelho
,
M. Vasconcelos
,
O. Nascimento
Molecular Cytogenetics
2016
Corpus ID: 2092103
Autism Spectrum Disorders (ASD) now encompass a broad heterogeneous group of people who present in the early developmental years…
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Review
2011
Review
2011
KLRK1 (killer cell lectin-like receptor subfamily K, member 1)
L. Lanier
2011
Corpus ID: 84591199
Review on KLRK1 (killer cell lectin-like receptor subfamily K, member 1), with data on DNA, on the protein encoded, and where the…
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2009
2009
Bivariate Genome‐Wide Linkage Analysis of Femoral Bone Traits and Leg Lean Mass: Framingham Study
D. Karasik
,
Yanhua Zhou
,
L. Cupples
,
M. Hannan
,
D. Kiel
,
S. Demissie
Journal of Bone and Mineral Research
2009
Corpus ID: 24594926
The risk of osteoporotic fracture is a function of both applied muscle mass and bone tissue distribution. Leg lean mass (LLM) and…
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2009
2009
Impact of 789Ala/Ala genotype on quantitative type of von Willebrand disease
F. Ahmad
,
M. Kannan
,
A. Biswas
,
R. Saxena
Annals of Hematology
2009
Corpus ID: 23426031
Abstractvon Willebrand factor (VWF) is a complex multimeric plasma glycoprotein encoded by an approximately 178-kb large VWF gene…
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2008
2008
Sequence of Genetic Events in ETV6-RUNX1 Positive B Precursor ALL: Insights from Identical Twins with Concordant Leukaemia
C. Bateman
,
S. Horsley
,
+4 authors
M. Greaves
2008
Corpus ID: 221004190
Monozygotic twin pairs with concordant ALL have provided unique insights into the molecular pathogenesis and natural history of…
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Review
2004
Review
2004
No association between a previously reported OLR1 3′ UTR polymorphism and Alzheimer’s disease in a large family sample
L. Bertram
,
M. Parkinson
,
K. Mullin
,
R. Menon
,
D. Blacker
,
R. Tanzi
Journal of Medical Genetics
2004
Corpus ID: 46065904
Recently, two studies1,2 reported independent evidence of genetic association between a 3′ UTR single nucleotide polymorphism…
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1998
1998
A frequent mutation in the acidic proline‐rich protein gene, PRH2, causing a Q147K change closely adjacent to the bacterial binding domain of the cognate salivary PRP (Pr1′) in Afro‐Americans
E. Azen
Human Mutation
1998
Corpus ID: 29388141
The human salivary proline‐rich proteins (PRPs) are coded by six closely linked genes on chromosome 12p13.2. Two of the PRP genes…
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1996
1996
Cloning, expression pattern and mapping to 12p 13.2 --> p13.1 of CLAPS3, a gene encoding a novel clathrin-adaptor small chain.
T. Watanabe
,
F. Shimizu
,
+5 authors
Y. Hirai
Cytogenetics and Cell Genetics
1996
Corpus ID: 46841612
From a human fetal-brain cDNA library we isolated a novel gene encoding a peptide homologous to clathrin-adaptor small chains in…
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1991
1991
The gene for the type 1 tumor necrosis factor receptor (TNF-R1) is localized on band 12p13
J. Derré
,
O. Kemper
,
D. Chérif
,
Y. Nophar
,
R. Berger
,
D. Wallach
Human Genetics
1991
Corpus ID: 30270670
SummaryThe gene coding for the type I (p55) tumor necrosis factor receptor (TNF-R1) has been localized on human chromosome 12…
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1985
1985
Localization of the human salivary protein complex (SPC) to chromosome band 12p13.2.
P. W. Mamula
,
N. Heerema
,
C. Palmer
,
K. Lyons
,
R. C. Karn
Cytogenetics and Cell Genetics
1985
Corpus ID: 20424017
In situ hybridization of a 3H-labeled probe containing a fragment from PRP-1, a genomic clone with human salivary proline-rich…
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