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12p12.3

A chromosome band present on 12p
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Urolithiasis, a complex multifactorial disease, results from interactions between environmental and genetic factors… 
Highly Cited
2015
Highly Cited
2015
IMPORTANCE Use of aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with lower risk of colorectal… 
Highly Cited
2006
Highly Cited
2006
Meniere's disease (MD) is characterized by spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, tinnitus, and… 
Highly Cited
2001
Highly Cited
2001
Type A receptors of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, contain alpha, beta, delta, gamma, and rho… 
Highly Cited
1999
Highly Cited
1999
Keutel syndrome (KS, MIM 245150) is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral… 
1999
1999
FISH analyses and loss of heterozygosity studies have delineated a commonly deleted region in hematological malignancies flanked… 
Review
1999
Review
1999
Cytogenetic deletions on the short arm of chromosome 12 are common, recurring alterations found in a wide range of hematological… 
Highly Cited
1997
Highly Cited
1997
Identification of the key genetic alterations leading to ovarian cancer is in its infancy. Polymerase chain reaction (PCR)-based… 
Highly Cited
1996
Highly Cited
1996
Together with the 31-kDa microfibril-associated glycoprotein (MAGP), four polypeptides designated MP340 (340 kDa), MP78 (78 kDa…