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Model organisms[edit]

Model organisms have been used in the study of CADM1 function. A conditional knockout mouse line, called Cadm1tm1.2Brd[4] was generated.[5] Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[3][6] Twenty six tests were carried out on homozygous mutant mice and one significant abnormality was observed: males were infertile.[3] Further analysis showed spermatogenesis had arrested in these mice.[5]

References[edit]

  1. ^ "Salmonella infection data for Cadm1". Wellcome Trust Sanger Institute.
  2. ^ "Citrobacter infection data for Cadm1". Wellcome Trust Sanger Institute.
  3. ^ a b c Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Opthalmologica 88: 925-7.doi:10.1111/j.1755-3768.2010.4142.x: Wiley.{{cite web}}: CS1 maint: location (link)
  4. ^ "Mouse Genome Informatics".
  5. ^ a b Van Der Weyden, L.; Arends, M. J.; Chausiaux, O. E.; Ellis, P. J.; Lange, U. C.; Surani, M. A.; Affara, N.; Murakami, Y.; Adams, D. J.; Bradley, A. (2006). "Loss of TSLC1 Causes Male Infertility Due to a Defect at the Spermatid Stage of Spermatogenesis". Molecular and Cellular Biology. 26 (9): 3595–3609. doi:10.1128/MCB.26.9.3595-3609.2006. PMC 1447413. PMID 16611999.
  6. ^ van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biol. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMID 21722353.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)