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4q13.3

A chromosome band present on 4q
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Cystic fibrosis (CF) is a monogenic disease due to mutations in the CFTR gene. Yet, variability in CF disease presentation is… Expand
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Highly Cited
2008
Highly Cited
2008
Integration of human papillomavirus (HPV) DNA into the host genome is a frequent event in cervical carcinogenesis and is reported… Expand
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2007
2007
In this study, we have elucidated the chromosomal imbalances in the multistep pathogenesis and delineated several critical tumor… Expand
2006
2006
Susceptibility to multiple sclerosis (MS) is believed to result from the complex interaction of a number of genes, each with… Expand
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2004
2004
We report the identification and functional analysis of a type II transmembrane serine protease encoded by the mouse… Expand
Highly Cited
2003
Highly Cited
2003
The genetic basis of non-syndromic autosomal recessive forms of amelogenesis imperfecta (AI) is unknown. To evaluate five… Expand
2003
2003
The amelogenesis imperfectas (AI) are a group of hereditary enamel defects characterized by clinical and genetic diversity. The… Expand
Highly Cited
2002
Highly Cited
2002
Seasonal allergic rhinitis (SAR) is an inflammatory disease of the nose and eyes that follows sensitization to air-born pollens… Expand
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Highly Cited
2000
Highly Cited
2000
Glucuronidation is a major pathway of androgen metabolism and is catalyzed by UDP-glucuronosyltransferase (UGT) enzymes. UGT2B15… Expand
Highly Cited
1998
Highly Cited
1998
In the fission yeast Schizosaccharomyces pombe the rad17 + gene is required for both the DNA damage-dependent and the DNA… Expand
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