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1p36.12

A chromosome band present on 1p
National Institutes of Health

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4 relations
C1QA wt AlleleChromosome 1 Short ArmChromosomesKDM1A wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk
There is a growing body of evidence suggesting that type 1 diabetes (T1D) is a genetically heterogeneous disease. However, the… 
2018
2018
Analyse génétique de patients consanguins Marocains atteints de la maladie de Parkinson combinant puce à ADN et panel de gènes
2016
2016
Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.
Genome-wide association studies (GWAS) have identified markers within the WNT4 region on chromosome 1p36.12 showing consistent… 
2008
2008
Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1–PRDM16 fusion in a case of progressive chronic myeloid leukemia: A complex chromosomal rearrangement of…
Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by the presence in leukemic stem cells of the… 
2005
2005
Genetic and Expressional Studies of Alzheimer's Disease
The aging of the population as result of elongated life expectancy will increase also the number of individuals affected by… 
2004
2004
Characterization and expression of the human WNT4; lack of associated germline mutations in high--to moderate--risk breast and ovarian cancer.
2003
2003
A novel ubiquitin‐specific protease, synUSP, is localized at the post‐synaptic density and post‐synaptic lipid raft
Recent reports suggest an important role for protein ubiquitination in synaptic plasticity. We cloned, from the rat brain, a… 
2001
2001
KUOPION YLIOPISTO UNIVERSITY OF KUOPIO
Alzheimer’s disease (AD) is the most common cause of progressive neurological disorder leading to dementia. It is… 
2000
2000
Genome-wide linkage disequilibrium mapping of late onset Alzheimer's disease in Finland
1995
1995
Determination and regional assignment of grouped sets of microclones in chromosome 1pter-p35.
In an approach to mapping physically the most distal 30 Mb of human chromosome 1p, region-specific clone libraries were generated… 
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