All you wanted to know about spermatogonia but were afraid to ask.
By D. G. Rooij, L. Russell. Journal of Andrology, 2000
940 citations recorded by the source corpus.
Subfields: General Health Professions, Philosophy
View Paper: https://www.semanticscholar.org/paper/9efcde93e959d4dfb8f2245142211c78498a892f
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- C. Tomasetti
- Christina Ernst
- Nils Eling
- Bert Vogelstein
- P. Boer
- C. Martinez-Jimenez
- Duncan T. Odom
- John C. Marioni
Citations in the corpus
- Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis (2018, background): “These cells have competency to undergo spermatogonial differentiation, which involves six transit-amplifying mitotic divisions generating A1-4, Intermediate, and B spermatogonia, which then give rise to pre-leptotene spermatocytes (pL) (de Rooij and Russell, 2000).”
- In vitro cytotoxicity of nanoparticles in mammalian germline stem cells. (2005, neutral): “The cells were immortalized using the large T antigen gene and exhibit a phenotype characteristic of germline stem cells in vivo, such as the expression of the Ret and GFRa-1 surface receptors and of the nuclear factor Oct-4 (de Rooij and Russell, 2000; Pesce et al., 1998; Hofmann et al., 2005b).”
- Specific arrests of spermatogenesis in genetically modified and mutant mice (2004, background): “Spermatogonial stem cells are single cells located on the basal membrane of the seminiferous tubules and are called A-single (As) spermatogonia (review de Rooij and Russell, 2000).”
- Variation in cancer risk among tissues can be explained by the number of stem cell divisions (2015, background): “03%) (142, 143), the average number of spermatozoa present in a human male can be calculated to be ~2.”