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TBC1D25 gene

Known as: TBC1 DOMAIN FAMILY, MEMBER 25, TBC1D25, ORNITHINE AMINOTRANSFERASE-LIKE 1 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
A possible role of Atg8 homologs as a scaffold for signal transduction
Atg8 and its homologs are essential for autophagosome formation in various species. In animal cells, Atg8 homologs have an… 
2010
2010
Association of Polyaminergic Loci With Anxiety, Mood Disorders, and Attempted Suicide
Background The polyamine system has been implicated in a number of psychiatric conditions, which display both alterations in… 
1995
1995
Long-range organization of reiterated sequences, including the SSX1 cDNA at the OATL1 cluster in Xp11.23.
Analysis of four YACs at the OATL1 locus was undertaken to determine the organization of locally repeated sequences within the… 
1995
1995
A high-resolution map of genes, microsatellite markers, and new dinucleotide repeats from UBE1 to the GATA locus in the region Xp11.23.
Several new genes and markers have recently been identified on the proximal short arm of the human X chromosome in the area of… 
Highly Cited
1994
Highly Cited
1994
The t(X;18)(p11.2;q11.2) translocation found in human synovial sarcomas involves two distinct loci on the X chromosome.
A high proportion of synovial sarcomas contain the reciprocal translocation t(X;18)(p11.2;q11.2). We have previously localized… 
1994
1994
Refined mapping of the human Ets-related gene Elk-1 to Xp11.2–p11.4, distal to the OATL1 region
The gene for human Elk-1, an Ets-related transcription factor, has previously been localized to a region that lies on the short… 
1993
1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YAC.
Using an ornithine-delta-aminotransferase (OAT) cDNA, we identified five YACs that cover two nonadjacent OAT-related loci in Xp11… 
1993
1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.
Norrie disease is a rare disease of newborn males caused by prenatal or perinatal retinal detachment, which may be associated… 
1993
1993
Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome.
Nonspecific X-linked mental retardation (MRX) includes several distinct entities with mental retardation but without additional… 
1991
1991
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm.
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