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2 documents found
1: Title: Homozygous in-frame deletion in CATSPERE in a man producing spermatozoa with loss of CatSper function and compromised fertilizing capacity.
Authors: Brown, Sean G, et.al. .
Journal: Human reproduction (Oxford, England) (Hum Reprod), Vol. 33 (10): 1812-1816, 2018 .
Snippet: STUDY DESIGN, SIZE, DURATION: This was a basic medical research study analysing genomic data from a single patient (patient 1) for defects in CATSPERE and CATSPERZ.
Affiliation: School of Science, Engineering & Technology, Abertay University, Dundee, UK. Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA. School of Biosciences, the University of Birmingham, Birmingham, UK. Reproductive and Developmental Biology, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK. Assisted Conception Unit, Ninewells Hospital, Dundee, UK. .
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2: Title: CatSperĪ¶ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility.
Authors: Chung, Jean-Ju, et.al. .
Journal: eLife, Vol. 6, 2017 .
Snippet: Ejaculated CatSperz-null sperm cells retrieved from the mated female uterus partially rescue in vitro fertilization (IVF) that failed with epididymal spermatozoa alone.
Affiliation: Howard Hughes Medical Institute, Boston Children's Hospital, Boston, United States. Department of Neurobiology, Harvard Medical School, Boston, United States. Department of Cellular and Molecular Physiology, Yale School of Medicine, New Haven, United States. Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Harvard University, Cambridge, United States. Department of Physics, Harvard University, Cambridge, United States. Department of Medicine, James J. Perters VA Bronx, Icahn School of Medicine at Mount Sinai, New York, United States. .
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