224 related articles for article (PubMed ID: 19897936)
1. Characterization and linkage mapping of an ENU-induced mutant mouse with defective spermatogenesis.
Asano Y; Akiyama K; Tsuji T; Takahashi S; Noguchi J; Kunieda T
Exp Anim; 2009 Oct; 58(5):525-32. PubMed ID: 19897936
[TBL] [Abstract][Full Text] [Related]
2. A new ENU-induced mutant mouse with defective spermatogenesis caused by a nonsense mutation of the syntaxin 2/epimorphin (Stx2/Epim) gene.
Akiyama K; Akimaru S; Asano Y; Khalaj M; Kiyosu C; Masoudi AA; Takahashi S; Katayama K; Tsuji T; Noguchi J; Kunieda T
J Reprod Dev; 2008 Apr; 54(2):122-8. PubMed ID: 18277055
[TBL] [Abstract][Full Text] [Related]
3. Leydig cell hyperplasia in an ENU-induced mutant mouse with germ cell depletion.
Khalaj M; Abbasi AR; Nishimura R; Akiyama K; Tsuji T; Noguchi J; Okuda K; Kunieda T
J Reprod Dev; 2008 Jun; 54(3):225-8. PubMed ID: 18385543
[TBL] [Abstract][Full Text] [Related]
4. Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene.
Rinchik EM; Carpenter DA; Handel MA
Proc Natl Acad Sci U S A; 1995 Jul; 92(14):6394-8. PubMed ID: 7604002
[TBL] [Abstract][Full Text] [Related]
5. An ENU-induced mutation in the mouse Rnf212 gene is associated with male meiotic failure and infertility.
Fujiwara Y; Matsumoto H; Akiyama K; Srivastava A; Chikushi M; Ann Handel M; Kunieda T
Reproduction; 2015 Jan; 149(1):67-74. PubMed ID: 25342176
[TBL] [Abstract][Full Text] [Related]
6. Arrest of spermatogenesis at the early meiotic stage in the small testis mutant (Smt) mice.
Bolor H; Zhao WD; Ishikawa A; Wakasugi N
Exp Anim; 2005 Jul; 54(4):327-37. PubMed ID: 16093646
[TBL] [Abstract][Full Text] [Related]
7. Abnormal spermatogenesis and male infertility in testicular zinc finger protein Zfp318-knockout mice.
Ishizuka M; Ohtsuka E; Inoue A; Odaka M; Ohshima H; Tamura N; Yoshida K; Sako N; Baba T; Kashiwabara S; Okabe M; Noguchi J; Hagiwara H
Dev Growth Differ; 2016 Sep; 58(7):600-8. PubMed ID: 27385512
[TBL] [Abstract][Full Text] [Related]
8. Mea2/Golga3 gene is disrupted in a line of transgenic mice with a reciprocal translocation between Chromosomes 5 and 19 and is responsible for a defective spermatogenesis in homozygotes.
Matsukuma S; Kondo M; Yoshihara M; Matsuda M; Utakoji T; Sutou S
Mamm Genome; 1999 Jan; 10(1):1-5. PubMed ID: 9892724
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel genetic loci for bone size and mechanosensitivity in an ENU mutant exhibiting decreased bone size.
Srivastava AK; Kapur S; Mohan S; Yu H; Kapur S; Wergedal J; Baylink DJ
J Bone Miner Res; 2005 Jun; 20(6):1041-50. PubMed ID: 15883645
[TBL] [Abstract][Full Text] [Related]
10. Seipin deficiency increases chromocenter fragmentation and disrupts acrosome formation leading to male infertility.
El Zowalaty AE; Baumann C; Li R; Chen W; De La Fuente R; Ye X
Cell Death Dis; 2015 Jul; 6(7):e1817. PubMed ID: 26181198
[TBL] [Abstract][Full Text] [Related]
11. Transgene insertion induced dominant male sterility and rescue of male fertility using round spermatid injection.
Meng X; Akutsu H; Schoene K; Reifsteck C; Fox EP; Olson S; Sariola H; Yanagimachi R; Baetscher M
Biol Reprod; 2002 Mar; 66(3):726-34. PubMed ID: 11870080
[TBL] [Abstract][Full Text] [Related]
12. The Hsp70 homolog gene, Hsc70t, is expressed under translational control during mouse spermiogenesis.
Tsunekawa N; Matsumoto M; Tone S; Nishida T; Fujimoto H
Mol Reprod Dev; 1999 Apr; 52(4):383-91. PubMed ID: 10092118
[TBL] [Abstract][Full Text] [Related]
13. Usp26 mutation in mice leads to defective spermatogenesis depending on genetic background.
Sakai K; Ito C; Wakabayashi M; Kanzaki S; Ito T; Takada S; Toshimori K; Sekita Y; Kimura T
Sci Rep; 2019 Sep; 9(1):13757. PubMed ID: 31551464
[TBL] [Abstract][Full Text] [Related]
14. Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis.
Endo T; Freinkman E; de Rooij DG; Page DC
Proc Natl Acad Sci U S A; 2017 Nov; 114(47):E10132-E10141. PubMed ID: 29109271
[TBL] [Abstract][Full Text] [Related]
15. Targeted disruption of Nphp1 causes male infertility due to defects in the later steps of sperm morphogenesis in mice.
Jiang ST; Chiou YY; Wang E; Lin HK; Lee SP; Lu HY; Wang CK; Tang MJ; Li H
Hum Mol Genet; 2008 Nov; 17(21):3368-79. PubMed ID: 18684731
[TBL] [Abstract][Full Text] [Related]
16. Mutation of Eif4g3, encoding a eukaryotic translation initiation factor, causes male infertility and meiotic arrest of mouse spermatocytes.
Sun F; Palmer K; Handel MA
Development; 2010 May; 137(10):1699-707. PubMed ID: 20430745
[TBL] [Abstract][Full Text] [Related]
17. Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility.
Dix DJ; Allen JW; Collins BW; Mori C; Nakamura N; Poorman-Allen P; Goulding EH; Eddy EM
Proc Natl Acad Sci U S A; 1996 Apr; 93(8):3264-8. PubMed ID: 8622925
[TBL] [Abstract][Full Text] [Related]
18. Systematic characterization of human testis-specific actin capping protein β3 as a possible biomarker for male infertility.
Soda T; Miyagawa Y; Ueda N; Takezawa K; Okuda H; Fukuhara S; Fujita K; Kiuchi H; Uemura M; Okamoto Y; Tsujimura A; Tanaka H; Nonomura N
Hum Reprod; 2017 Mar; 32(3):514-522. PubMed ID: 28104696
[TBL] [Abstract][Full Text] [Related]
19. A spontaneous smc1b mutation causes cohesin protein dysfunction and sterility in mice.
Takabayashi S; Yamauchi Y; Tsume M; Noguchi M; Katoh H
Exp Biol Med (Maywood); 2009 Aug; 234(8):994-1001. PubMed ID: 19491376
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic characterization of a new Grin1 mutant mouse generated by ENU mutagenesis.
Furuse T; Wada Y; Hattori K; Yamada I; Kushida T; Shibukawa Y; Masuya H; Kaneda H; Miura I; Seno N; Kanda T; Hirose R; Toki S; Nakanishi K; Kobayashi K; Sezutsu H; Gondo Y; Noda T; Yuasa S; Wakana S
Eur J Neurosci; 2010 Apr; 31(7):1281-91. PubMed ID: 20345915
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
