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… (More)

Topic mentions per year

Topic mentions per year

1986-2016
02419862016

Papers overview

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2013
2013
OBJECTIVE Law enforcement represents a large population of workers who may be exposed to electronic control devices (ECDs… (More)
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2011
2011
BACKGROUND Early child health and development (ECD) is important for health in later life. Objectives were to (1) examine the… (More)
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2009
2009
OBJECTIVES RA is associated with endothelial cell dysfunction (ECD) and increased cardiovascular mortality and morbidity… (More)
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2006
2006
The present study used magnetoencephalography (MEG) to investigate human MT/V5 activity when observing changes in eye gaze… (More)
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2000
2000
OBJECTIVES Accurate prediction of outcome in acute stroke would help in identifying subgroups of patients for therapeutic trials… (More)
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1998
1998
In an attempt to elucidate the neural generators of pattern reversal visual evoked potentials (PR-VEPs), we measured the visual… (More)
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1997
1997
The accumulation of 99mTc-HMPAO and 99mTc-ECD was studied in rat (MatB) and human (MCF-7) breast tumor cell lines in vitro as a… (More)
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Highly Cited
1995
Highly Cited
1995
We have isolated and chromosomally fine-mapped 16 novel genes belonging to the human zinc finger Krüppel family (ZNF131-140, 142… (More)
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1994
1994
Split hand/split foot (SHSF; also known as ectrodactyly) is a human developmental disorder characterized by missing central… (More)
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1994
1994
Ectrodactyly (split hand/split foot, SHSF) is characterized by the absence of middle rays of the hand or the foot. Cytogenetic… (More)
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