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SHFM1 wt Allele

Known as: Split Hand/Foot Malformation (Ectrodactyly) Type 1 wt Allele, ECD, Deleted In Split-Hand/Split-Foot 1 Region 
Human SHFM1 wild-type allele is located within 7q21.3-q22.1 and is approximately 21 kb in length. This allele, which encodes 26 proteasome complex… Expand
National Institutes of Health

Papers overview

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2014
2014
UNLABELLED Semen enhances HIV infection in vitro, but how long it retains this activity has not been carefully examined… Expand
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Split hand and foot malformation (SHFM) refers to a genetically heterogeneous developmental disorder of the hands and… Expand
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Highly Cited
2009
Highly Cited
2009
The evolutionarily conserved protein Sem1/Dss1 is a subunit of the regulatory particle (RP) of the proteasome, and, in mammalian… Expand
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Highly Cited
2008
Highly Cited
2008
We used a quantitative, high-density genetic interaction map, or E-MAP (Epistatic MiniArray Profile), to interrogate the… Expand
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Highly Cited
2004
Highly Cited
2004
Degradation of polyubiquitinated proteins by the proteasome often requires accessory factors; these include receptor proteins… Expand
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Highly Cited
2004
Highly Cited
2004
The 26 S proteasome, which catalyzes degradation of polyubiquitinated proteins, is composed of the 20 S proteasome and the 19 S… Expand
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2004
2004
Split hand/foot malformation type I (SHFM1, OMIM *183600) is an autosomal dominant developmental disorder of limb formation that… Expand
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Highly Cited
2001
Highly Cited
2001
The disease-specific survival (DSS) of 151 patients with chronic graft-versus-host disease (cGVHD) was studied in an attempt to… Expand
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Highly Cited
1994
Highly Cited
1994
Split hand/split foot (ectrodactyly; SHSF) is a human developmental malformation characterized by missing digits and claw-like… Expand
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Review
1994
Review
1994
Split hand/split foot (SHFD) is a human developmental defect characterized by missing digits, fusion of remaining digits, and a… Expand
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