Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland-Reference-Cited by-同舟云学术

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland

Published:2015-02 Issue:1 Volume:29 Page:31-34
ISSN:0890-8508
Container-title:Molecular and Cellular Probes
language:en
Short-container-title:Molecular and Cellular Probes

Author:

Schubert Stephanie,Haas Cordula,Bartsch Christine,Mirshekarnejad Mandana,Kohrs Sarah,Roettinger Irene,Grosshennig Anika,Stuhrmann Manfred,Scholz Caroline,Schmidtke Jörg

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference14 articles.

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2. Concurrent risks in sudden infant death syndrome;Ostfeld;Pediatrics,2010

3. Genetics of the sudden infant death syndrome;Courts;Forensic Sci Int,2010

4. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome;Van Norstrand;Circulation,2007

5. Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function;Puffenberger;Proc Natl Acad Sci U S A,2004

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1. Using Selenium-enriched Mutated Probiotics as Enhancer for Fertility Parameters in Mice;Biological Trace Element Research;2024-02-07

2. Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants;American Journal of Medical Genetics Part A;2022-09-09

3. TSPYL1 regulates steroidogenic gene expression and male factor fertility in mice;F&S Science;2020-11

4. Unravelling the disease mechanism for TSPYL1 deficiency;Human Molecular Genetics;2020-10-15

5. Battle of the sexes: contrasting roles of testis-specific protein Y-encoded (TSPY) and TSPX in human oncogenesis;Asian Journal of Andrology;2019