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FAM123B wt Allele

Known as: FLJ39827, RP11-403E24.2, Family with Sequence Similarity 123B wt Allele 
Human FAM123B wild-type allele is located in the vicinity of Xq11.1 and is approximately 21 kb in length. This allele, which encodes protein FAM123B… 
National Institutes of Health

Papers overview

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2018
2018
Monolithically integrated millimeter-wave wavelet transmitters are presented and analyzed in this paper. Two designs that include… 
2016
2016
Objective: Wilms’ tumor gene on the X chromosome (WTX) was reported to be a tumor-suppression gene for various cancers. The… 
2014
2014
WTX is a tumor suppressor gene expressed during embryonic development and inactivated in 20–30% of cases of Wilms tumor, the most… 
2014
2014
An integrated millimeter-wave wavelet transmitter has been fabricated and characterized. It consists of a generator core on a co… 
Highly Cited
2012
Highly Cited
2012
Somatic defects at five loci, WT1, CTNNB1, WTX, TP53 and the imprinted 11p15 region, are implicated in Wilms tumor, the commonest… 
2012
2012
BACKGROUND Wilms' tumor (nephroblastoma) is the most common pediatric kidney cancer. Only one Wilms' tumor gene is known, WT1 at… 
Review
2011
Review
2011
To the Editor: WTX is an X-linked gene found to be altered in Wilms tumor (WT) and proposed as an example of a tumor suppressor… 
Highly Cited
2008
Highly Cited
2008
For many years the precise genetic etiology of the majority of Wilms’ tumors has remained unexplained. Recently, the WTX gene… 
2008
2008
WTX (Wilms’ tumor gene on the X chromosome) is inactivated in 30% of Wilms’ tumors, mostly by chromosomal deletion.[1][1] The WTX…