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6p21.2

A chromosome band present on 6p
National Institutes of Health

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5 relations
CDKN1A wt AlleleChromosome 6 Short ArmChromosomesPIM1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
The role of TP53 and p21 gene polymorphisms in breast cancer biology in a well specified and characterized German cohort
ObjectiveAbrogation of the function of TP53 gene is supposed to lead to a more aggressive breast cancer phenotype that produces a… 
Review
2009
Review
2009
[Advances in genetics of restless legs syndrome].
Recent advances in genetic studies on restless legs syndrome (RLS) have led to a series of important discoveries that greatly… 
2006
2006
Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF
Kosuke Izumi, Naohisa Yahagi, Yasushi Fujii, Masataka Higuchi, Rika Kosaki, Yoko Naito, Gen Nishimura, Noboru Hosokai, Takao… 
2006
2006
Loss of heterozygosity at chromosome 6 as a marker of early genetic alterations in cervical intraepithelial neoplasias and microinvasive carcinomas
Oncogenic human papillomaviruses (mostly HPV types 16 and 18) are the major cause of cervical intraepithelial neoplasia (CIN… 
2002
2002
Characterization of a novel hematopoietic marker expressed from early embryonic hematopoietic stem cells to adult mature lineages.
A novel membrane protein has been identified in the course of screening for differentially expressed cDNAs in human embryonic… 
2000
2000
Loss of heterozygosity on chromosome 6p21.2 as a potential marker for recurrence after radiotherapy of human cervical cancer.
Cervical carcinomas develop as a result of multiple genetic alterations, and specific alterations lead to specific clinical… 
2000
2000
Construction of a high-resolution 2.5-Mb transcript map of the human 6p21.2-6p21.3 region immediately centromeric of the major histocompatibility complex.
We have constructed a 2.5-Mb physical and transcription map that spans the human 6p21.2-6p21.3 region and includes the… 
1999
1999
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
FGD1 encodes a guanine nucleotide exchange factor (GEF) that specifically activates the Rho GTPase Cdc42. FGD1 gene mutations… 
1998
1998
Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex.
We have physically mapped and cloned a 2.5-Mb chromosomal segment flanking the centromeric end of the major histocompatibility… 
1996
1996
A rat mutation producing demyelination (dmy) maps to chromosome 17
A recessive mutation exhibiting severe myelin breakdown, mainly at the level of the lumbar segments of the spinal cord and… 
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