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2. High-resolution mapping of sperm function defects in the t complex fourth inversion. Redkar AA; Olds-Clarke P; Dugan LM; Pilder SH Mamm Genome; 1998 Oct; 9(10):825-30. PubMed ID: 9745038 [TBL] [Abstract][Full Text] [Related]
3. An axonemal dynein at the Hybrid Sterility 6 locus: implications for t haplotype-specific male sterility and the evolution of species barriers. Fossella J; Samant SA; Silver LM; King SM; Vaughan KT; Olds-Clarke P; Johnson KA; Mikami A; Vallee RB; Pilder SH Mamm Genome; 2000 Jan; 11(1):8-15. PubMed ID: 10602986 [TBL] [Abstract][Full Text] [Related]
4. Hst7: a male sterility mutation perturbing sperm motility, flagellar assembly, and mitochondrial sheath differentiation. Pilder SH; Olds-Clarke P; Orth JM; Jester WF; Dugan L J Androl; 1997; 18(6):663-71. PubMed ID: 9432139 [TBL] [Abstract][Full Text] [Related]
5. The mouse T complex gene Tsga2, encoding polypeptides located in the sperm tail and anterior acrosome, maps to a locus associated with sperm motility and sperm-egg interaction abnormalities. Hui L; Lu J; Han Y; Pilder SH Biol Reprod; 2006 Apr; 74(4):633-43. PubMed ID: 16354795 [TBL] [Abstract][Full Text] [Related]
6. Hybrid sterility-6: a mouse t complex locus controlling sperm flagellar assembly and movement. Pilder SH; Olds-Clarke P; Phillips DM; Silver LM Dev Biol; 1993 Oct; 159(2):631-42. PubMed ID: 8405685 [TBL] [Abstract][Full Text] [Related]
7. The molecular basis of "curlicue": a sperm motility abnormality linked to the sterility of t haplotype homozygous male mice. Pilder SH; Lu J; Han Y; Hui L; Samant SA; Olugbemiga OO; Meyers KW; Cheng L; Vijayaraghavan S Soc Reprod Fertil Suppl; 2007; 63():123-33. PubMed ID: 17566267 [TBL] [Abstract][Full Text] [Related]
8. A novel mouse chromosome 17 hybrid sterility locus: implications for the origin of t haplotypes. Pilder SH; Hammer MF; Silver LM Genetics; 1991 Sep; 129(1):237-46. PubMed ID: 1936961 [TBL] [Abstract][Full Text] [Related]
9. Genes in the first and fourth inversions of the mouse t complex synergistically mediate sperm capacitation and interactions with the oocyte. Redkar AA; Si Y; Twine SN; Pilder SH; Olds-Clarke P Dev Biol; 2000 Oct; 226(2):267-80. PubMed ID: 11023686 [TBL] [Abstract][Full Text] [Related]
10. The cellular basis for interaction of sterility factors in the mouse t haplotype. Johnson LR; Pilder SH; Olds-Clarke P Genet Res; 1995 Dec; 66(3):189-93. PubMed ID: 8600017 [TBL] [Abstract][Full Text] [Related]
11. Genetic analysis of X-linked hybrid sterility in the house mouse. Storchová R; Gregorová S; Buckiová D; Kyselová V; Divina P; Forejt J Mamm Genome; 2004 Jul; 15(7):515-24. PubMed ID: 15366371 [TBL] [Abstract][Full Text] [Related]
12. The lack of Tex44 causes severe subfertility with flagellar abnormalities in male mice. Dupuis S; Girault MS; Le Beulze M; Ialy-Radio C; Bermúdez-Guzmán L; Ziyyat A; Barbaux S Cell Mol Biol Lett; 2024 May; 29(1):74. PubMed ID: 38750428 [TBL] [Abstract][Full Text] [Related]
13. The mouse t complex distorter/sterility candidate, Dnahc8, expresses a gamma-type axonemal dynein heavy chain isoform confined to the principal piece of the sperm tail. Samant SA; Ogunkua OO; Hui L; Lu J; Han Y; Orth JM; Pilder SH Dev Biol; 2005 Sep; 285(1):57-69. PubMed ID: 16054618 [TBL] [Abstract][Full Text] [Related]
14. Models for male infertility: the t haplotypes. Olds-Clarke P Rev Reprod; 1997 Sep; 2(3):157-64. PubMed ID: 9414479 [TBL] [Abstract][Full Text] [Related]
15. Mutations in a novel locus on mouse chromosome 11 resulting in male infertility associated with defects in microtubule assembly and sperm tail function. Clark AT; Firozi K; Justice MJ Biol Reprod; 2004 May; 70(5):1317-24. PubMed ID: 14711786 [TBL] [Abstract][Full Text] [Related]
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18. Male Infertility Is Responsible for Nearly Half of the Extinction Observed in the Mouse Collaborative Cross. Shorter JR; Odet F; Aylor DL; Pan W; Kao CY; Fu CP; Morgan AP; Greenstein S; Bell TA; Stevans AM; Feathers RW; Patel S; Cates SE; Shaw GD; Miller DR; Chesler EJ; McMillian L; O'Brien DA; Villena FP Genetics; 2017 Jun; 206(2):557-572. PubMed ID: 28592496 [TBL] [Abstract][Full Text] [Related]
19. Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia. Rashid S; Grzmil P; Drenckhahn JD; Meinhardt A; Adham I; Engel W; Neesen J Reproduction; 2010 Jan; 139(1):99-111. PubMed ID: 19778998 [TBL] [Abstract][Full Text] [Related]
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