FBXW4 gene

Known as: DACTYLIN, F-box and WD repeat domain containing 4, SHFM3, FORMERLY 
This gene plays a role in both protein turnover and embryonic limb development.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2017
02419992017

Papers overview

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2017
2017
OBJECTIVE To determine the genomic signatures of human uterine leiomyomas and prevalence of MED12 mutations in human uterine… (More)
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2013
2013
Identification of novel proteins that can potentially contribute to carcinogenesis is a requisite venture. Herein, we report the… (More)
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2012
2012
Split hand/foot malformation (SHFM) is a congenital disorder characterized by a cleft of the hands and/or feet due to dificiency… (More)
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2007
2007
Dactylaplasia, characterized by missing central digital rays, is an inherited mouse limb malformation that depends on two genetic… (More)
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2005
2005
Split-hand/split-foot malformation (SHFM) is a congenital limb malformation characterized by a median cleft of hand and/or foot… (More)
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2005
2005
RECENT investigations of the relationship of various constituents of pollens to the allergic diseases for which they are… (More)
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2003
2003
Split hand-split foot malformation (SHFM) is characterized by hypoplasia/aplasia of the central digits with fusion of the… (More)
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2003
2003
Split hand foot malformation (SHFM) is a congenital limb malformation presenting with a median cleft of the hand and/or foot… (More)
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2000
2000
Suppressor of fused (Sufu) is a negative regulator of the Hedgehog pathway both in Drosophila and vertebrates. Here, we report… (More)
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1999
1999
Early outgrowth of the vertebrate embryonic limb requires signalling by the apical ectodermal ridge (AER) to the progress zone… (More)
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