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ST7 wt Allele

Known as: RAY1, TSG7, Suppression of Tumorigenicity 7 wt Allele 
Human ST7 wild-type allele is located within 7q31.1-q31.3 and is approximately 277 kb in length. This allele, which encodes suppressor of… Expand
National Institutes of Health

Related topics

Related topics

7 relations
7q31.1-q31.3Cell Proliferation Regulatory ProcessHomo sapiensInhibition of Cancer Cell Growth
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Broader (1)

ST7 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
The novel helicase helG (DHX30) is expressed during gastrulation in mice and has a structure similar to a human DExH box helicase.
The gene trap method for embryonic stem cells is an efficient method for identifying new genes that are involved in development… Expand
2015
2015
The Novel Helicase helG (DHX30) Is Expressed During Gastrulation in Mice and Has a Structure Similar to a Human DExH Box Helicase
The gene trap method for embryonic stem cells is an efficient method for identifying new genes that are involved in development… Expand
2013
2013
Arabinosylation of a Yariv-precipitable cell wall polymer impacts plant growth as exemplified by the Arabidopsis glycosyltransferase mutant ray1.
 
2010
2010
Power dissipation for systems with junctions of multiple quantum wires
We study power dissipation for systems of multiple quantum wires meeting at a junction, in terms of a current splitting matrix (M… Expand
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2004
2004
La formación de valores en la historia de la educación colombiana
En esta época la universidad colonial se orientó a formar a la elite criolla y española en profesiones como el Derecho y el… Expand
2002
2002
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.
We recently identified a novel gene, RAY1 (FAM4A1), which spans a translocation breakpoint at 7q31 in a patient with autism. This… Expand
Highly Cited
2001
Highly Cited
2001
Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31
Loss of heterozygosity (LOH) of markers on human chromosome 7q31 is frequently encountered in a variety of human neoplasias… Expand
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Highly Cited
2000
Highly Cited
2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.
The results of genetic linkage studies for autism have suggested that a susceptibility locus for the disease is located on the… Expand
1949
1949
Matrix representation of models for the analysis of variance and covariance
  • P. Rulon
  • Psychometrika
  • 1949
    • Corpus ID: 38670169
Beginning students of analysis of variance frequently find that the explanations concerning numbers of degrees of freedom are… Expand
1936
1936
Estimation of Ascorbic Acid (Vitamin C) by Titration
METHODS for the determination of ascorbic acid have recently been much discussed. Tillmans' method, as modified by Harris and… Expand
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