118 related articles for article (PubMed ID: 31880374)
21. DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.
Sha Y; Yang X; Mei L; Ji Z; Wang X; Ding L; Li P; Yang S
Fertil Steril; 2017 Jun; 107(6):1312-1318.e2. PubMed ID: 28577616
[TBL] [Abstract][Full Text] [Related]
22. Association of single nucleotide polymorphism c.673C>A/p.Gln225Lys in SEPT12 gene with spermatogenesis failure in male idiopathic infertility in Northeast China.
Geng D; Yang X; Zhang H; Liu X; Yu Y; Jiang Y; Liu R; Zhang G
J Int Med Res; 2019 Feb; 47(2):992-998. PubMed ID: 30488758
[TBL] [Abstract][Full Text] [Related]
23. Phospholipase C zeta parameters in sperm from polymorphic teratozoospermic men.
Azad N; Nazarian H; Ghaffari Novin M; Masteri Farahani R; Piryaei A; Heidari MH
Ann Anat; 2018 Jan; 215():63-70. PubMed ID: 28954206
[TBL] [Abstract][Full Text] [Related]
24. Evaluation of
Mazaheri Moghaddam M; Mazaheri Moghaddam M; Amini M; Bahramzadeh B; Baghbanzadeh A; Biglari A; Sakhinia E
Health Sci Rep; 2021 Dec; 4(4):e436. PubMed ID: 34849407
[TBL] [Abstract][Full Text] [Related]
25. Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.
Wang G; Zhu X; Gao Y; Lv M; Li K; Tang D; Wu H; Xu C; Geng H; Shen Q; Zha X; Duan Z; Zhang J; Hua R; Tao F; Zhou P; Wei Z; Cao Y; Guo R; He X
Hum Mutat; 2022 Dec; 43(12):2079-2090. PubMed ID: 36135717
[TBL] [Abstract][Full Text] [Related]
26. Septins at the annulus of mammalian sperm.
Toure A; Rode B; Hunnicutt GR; Escalier D; Gacon G
Biol Chem; 2011 Aug; 392(8-9):799-803. PubMed ID: 21740329
[TBL] [Abstract][Full Text] [Related]
27. Localization Patterns of RAB3C Are Associated with Murine and Human Sperm Formation.
Tsai YL; Lai TH; Liu HC; Wang YY; Lin YH; Ke CC; Chung MT; Chan CC; Lin YH
Medicina (Kaunas); 2022 Oct; 58(10):. PubMed ID: 36295569
[TBL] [Abstract][Full Text] [Related]
28. An intronic insertion in KPL2 results in aberrant splicing and causes the immotile short-tail sperm defect in the pig.
Sironen A; Thomsen B; Andersson M; Ahola V; Vilkki J
Proc Natl Acad Sci U S A; 2006 Mar; 103(13):5006-11. PubMed ID: 16549801
[TBL] [Abstract][Full Text] [Related]
29. The impact of RABL2B gene (rs144944885) on human male infertility in patients with oligoasthenoteratozoospermia and immotile short tail sperm defects.
Hosseini SH; Sadighi Gilani MA; Meybodi AM; Sabbaghian M
J Assist Reprod Genet; 2017 Apr; 34(4):505-510. PubMed ID: 28138870
[TBL] [Abstract][Full Text] [Related]
30. SEPT12 deficiency causes sperm nucleus damage and developmental arrest of preimplantation embryos.
Lin YH; Chou CK; Hung YC; Yu IS; Pan HA; Lin SW; Kuo PL
Fertil Steril; 2011 Jan; 95(1):363-5. PubMed ID: 20801438
[TBL] [Abstract][Full Text] [Related]
31. Alternative splicing, promoter methylation, and functional SNPs of sperm flagella 2 gene in testis and mature spermatozoa of Holstein bulls.
Guo F; Yang B; Ju ZH; Wang XG; Qi C; Zhang Y; Wang CF; Liu HD; Feng MY; Chen Y; Xu YX; Zhong JF; Huang JM
Reproduction; 2014 Feb; 147(2):241-52. PubMed ID: 24277870
[TBL] [Abstract][Full Text] [Related]
32. Oxidative stress and phenotype frequencies of paraoxonase-1 in teratozoospermia.
Ozer OF; Akbulut H; Guler EM; Caglar HG; Gevher F; Koktasoglu F; Selek S
Andrologia; 2019 Sep; 51(8):e13299. PubMed ID: 31012132
[TBL] [Abstract][Full Text] [Related]
33. Relationship between sperm DNA damage with sperm parameters, oxidative markers in teratozoospermic men.
Ammar O; Haouas Z; Hamouda B; Hamdi H; Hellara I; Jlali A; Cheikh HB; Mehdi M
Eur J Obstet Gynecol Reprod Biol; 2019 Feb; 233():70-75. PubMed ID: 30580226
[TBL] [Abstract][Full Text] [Related]
34. Absence of annulus in human asthenozoospermia: case report.
Lhuillier P; Rode B; Escalier D; Lorès P; Dirami T; Bienvenu T; Gacon G; Dulioust E; Touré A
Hum Reprod; 2009 Jun; 24(6):1296-303. PubMed ID: 19221096
[TBL] [Abstract][Full Text] [Related]
35. [Analysis of sperm chromosomes in infertile males with teratozoospermia].
Szczygieł MA; Kusakabe H; Wiland E; Kurpisz M
Ginekol Pol; 2003 Feb; 74(2):108-15. PubMed ID: 12715419
[TBL] [Abstract][Full Text] [Related]
36. Quantification of sperm specific mRNA transcripts (PRM1, PRM2, and TNP2) in teratozoospermia and normozoospermia: New correlations between mRNA content and morphology of sperm.
Savadi-Shiraz E; Edalatkhah H; Talebi S; Heidari-Vala H; Zandemami M; Pahlavan S; Modarressi MH; Akhondi MM; Paradowska-Dogan A; Sadeghi MR
Mol Reprod Dev; 2015 Jan; 82(1):26-35. PubMed ID: 25536093
[TBL] [Abstract][Full Text] [Related]
37. The expression characteristics of FAM71D and its association with sperm motility.
Ma Q; Li Y; Luo M; Guo H; Lin S; Chen J; Du Y; Jiang Z; Gui Y
Hum Reprod; 2017 Nov; 32(11):2178-2187. PubMed ID: 29025071
[TBL] [Abstract][Full Text] [Related]
38. Expression of NOX5 in human teratozoospermia compared to normozoospermia.
Ghani E; Keshtgar S; Habibagahi M; Ghannadi A; Kazeroni M
Andrologia; 2013 Oct; 45(5):351-6. PubMed ID: 23030296
[TBL] [Abstract][Full Text] [Related]
39. Genetic abnormalities leading to qualitative defects of sperm morphology or function.
Ray PF; Toure A; Metzler-Guillemain C; Mitchell MJ; Arnoult C; Coutton C
Clin Genet; 2017 Feb; 91(2):217-232. PubMed ID: 27779748
[TBL] [Abstract][Full Text] [Related]
40. Analysis of PRM1 and PRM2 Polymorphisms in Iranian Infertile Men with Idiopathic Teratozoospermia.
Dehghanpour F; Fesahat F; Miresmaeili SM; Zare Mehrjardi E; Honarju A; Talebi AR
Int J Fertil Steril; 2019 Apr; 13(1):77-82. PubMed ID: 30644249
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
