TSPYL1 抗体
(TSPY-Like 1 (TSPYL1))
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009].
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Latest Publications for our TSPYL1 抗体
: "Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells." in: Nature methods, Vol. 10, Issue 4, pp. 315-23, (2013) (PubMed).: "Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility." in: Fertility and sterility, Vol. 92, Issue 4, pp. 1347-50, (2009) (PubMed).
: "Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster." in: Blood cells, molecules & diseases, Vol. 37, Issue 2, pp. 82-90, (2006) (PubMed).
: "Genetic investigation of the TSPYL1 gene in sudden infant death syndrome." in: Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 8, Issue 1, pp. 55-8, (2006) (PubMed).
: "Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags." in: Biochemical and biophysical research communications, Vol. 345, Issue 3, pp. 1022-32, (2006) (PubMed).
: "Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 101, Issue 32, pp. 11689-94, (2004) (PubMed).
Aliases for TSPYL1 抗体
testis-specific protein, Y-encoded-like 1 (Tspyl1) 抗体TSPY like 1 (TSPYL1) 抗体
Tspyl 抗体
TSPYL 抗体
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