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17q11.1

A chromosome band present on 17q
National Institutes of Health

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3 relations
17qChromosomesKSR1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer
Chromothripsis is an event of genomic instability leading to complex chromosomal alterations in cancer. Frequent long-range… 
2008
2008
Association study of serotonin transporter gene polymorphisms with obstructive sleep apnea syndrome in Chinese Han population.
BACKGROUND Since the serotonin (5-HT) is associated with circadian rhythm and breathing regulation, the serotonin transporter (5… 
Highly Cited
2003
Highly Cited
2003
A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear… 
Highly Cited
2000
Highly Cited
2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
PURPOSE To map the locus for autosomal dominant cataracts (ADCs) in a Brazilian family using candidate gene linkage analyses… 
Highly Cited
1998
Highly Cited
1998
Serotonin Transporter Gene and Risk for Bipolar Affective Disorder: An Association Study in a Spanish Population
1997
1997
Genomic structure and genetic mapping of the human neutral cysteine protease bleomycin hydrolase.
Bleomycin hydrolase (BH) is the only known eukaryotic enzyme that inactivates the widely used antineoplastic agent bleomycin (BLM… 
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