12p12.3

A chromosome band present on 12p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1981-2018
024619812018

Papers overview

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2014
2014
Colorectal cancer (CRC) is one of the most common cancer worldwide. However, a large number of genetic risk factors involved in… (More)
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2011
2011
Purpose: To study the inheritance and characteristics of familial Meniere disease in Finland and genetic linkage to the… (More)
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2010
2010
Meniere's disease (MD) is a disorder of the inner ear characterized by episodes of vertigo, tinnitus and fluctuating… (More)
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2006
2006
Meniere's disease (MD) is characterized by spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, tinnitus, and… (More)
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2001
2001
Type A receptors of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, contain alpha, beta, delta, gamma, and rho… (More)
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Highly Cited
1999
Highly Cited
1999
Keutel syndrome (KS, MIM 245150) is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral… (More)
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1999
1997
1997
Identification of the key genetic alterations leading to ovarian cancer is in its infancy. Polymerase chain reaction (PCR)-based… (More)
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1997
1997
Cytogenetic deletions of the short arm of chromosome 12 are common recurring alterations found in a wide range of haematological… (More)
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1995
1995
CDKN4/p27Kip1 is a cyclin-dependent kinase (Cdk) inhibitor implicated in G1 phase arrest, which negatively regulates G1 phase… (More)
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