These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 22643004)

  • 1. [Morphological defects of sperm flagellum implicated in human male infertility].
    Escalier D; Touré A
    Med Sci (Paris); 2012 May; 28(5):503-11. PubMed ID: 22643004
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Knockout mouse models of sperm flagellum anomalies.
    Escalier D
    Hum Reprod Update; 2006; 12(4):449-61. PubMed ID: 16565154
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice.
    Wang YY; Ke CC; Chen YL; Lin YH; Yu IS; Ku WC; O'Bryan MK; Lin YH
    PLoS Genet; 2020 Sep; 16(9):e1009020. PubMed ID: 32976492
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Notulae seminologicae. 2. The 'short tail' and 'stump' defect in human spermatozoa.
    Baccetti B; Burrini AG; Capitani S; Collodel G; Moretti E; Piomboni P; Renieri T
    Andrologia; 1993; 25(6):331-5. PubMed ID: 8279704
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Light microscopy morphological characteristics of the sperm flagellum may be related to axonemal abnormalities.
    Mitchell V; Sigala J; Ballot C; Jumeau F; Barbotin AL; Duhamel A; Rives N; Rigot JM; Escalier D; Peers MC
    Andrologia; 2015 Mar; 47(2):214-20. PubMed ID: 24611953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.
    Sha Y; Liu W; Wei X; Zhu X; Luo X; Liang L; Guo T
    Clin Genet; 2019 Nov; 96(5):385-393. PubMed ID: 31278745
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Animal models: Candidate genes for human male infertility].
    Escalier D
    Gynecol Obstet Fertil; 2006 Sep; 34(9):827-30. PubMed ID: 16931095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Morphological sperm defects analyzed by light microscopy and transmission electron microscopy and their correlation with sperm motility.
    Visco V; Raffa S; Elia J; Delfino M; Imbrogno N; Torrisi MR; Mazzilli F
    Int J Urol; 2010 Mar; 17(3):259-66. PubMed ID: 20409218
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
    Dong FN; Amiri-Yekta A; Martinez G; Saut A; Tek J; Stouvenel L; Lorès P; Karaouzène T; Thierry-Mieg N; Satre V; Brouillet S; Daneshipour A; Hosseini SH; Bonhivers M; Gourabi H; Dulioust E; Arnoult C; Touré A; Ray PF; Zhao H; Coutton C
    Am J Hum Genet; 2018 Apr; 102(4):636-648. PubMed ID: 29606301
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypes of sperm pathology: genetic and acquired forms in infertile men.
    Chemes HE
    J Androl; 2000; 21(6):799-808. PubMed ID: 11105905
    [No Abstract]   [Full Text] [Related]  

  • 11. The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertility.
    Linck RW; Chemes H; Albertini DF
    J Assist Reprod Genet; 2016 Feb; 33(2):141-56. PubMed ID: 26825807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sperm tail agenesis in a case of consanguinity.
    Latini M; Gandini L; Lenzi A; Romanelli F
    Fertil Steril; 2004 Jun; 81(6):1688-91. PubMed ID: 15193497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Total asthenospermia with an ultrastructural anomaly of the flagellum in two sterile brothers (author's transl)].
    Alexandre C; Bisson JP; David G
    J Gynecol Obstet Biol Reprod (Paris); 1978 Jan; 7(1):31-8. PubMed ID: 641313
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
    Kherraf ZE; Amiri-Yekta A; Dacheux D; Karaouzène T; Coutton C; Christou-Kent M; Martinez G; Landrein N; Le Tanno P; Fourati Ben Mustapha S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Pernet-Gallay K; Gourabi H; Robinson DR; Crouzy S; Blum M; Thierry-Mieg N; Touré A; Zouari R; Arnoult C; Bonhivers M; Ray PF
    Am J Hum Genet; 2018 Sep; 103(3):400-412. PubMed ID: 30122540
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly.
    Brunner S; Colman D; Travis AJ; Luhmann UF; Shi W; Feil S; Imsand C; Nelson J; Grimm C; Rülicke T; Fundele R; Neidhardt J; Berger W
    Biol Reprod; 2008 Oct; 79(4):608-17. PubMed ID: 18579752
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel homozygous nonsense variant of AK7 is associated with multiple morphological abnormalities of the sperm flagella.
    Chang T; Tang H; Zhou X; He J; Liu N; Li Y; Xiang W; Yao Z
    Reprod Biomed Online; 2024 May; 48(5):103765. PubMed ID: 38492416
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel associations between specific sperm morphological defects and leukocytospermia.
    Aziz N; Agarwal A; Lewis-Jones I; Sharma RK; Thomas AJ
    Fertil Steril; 2004 Sep; 82(3):621-7. PubMed ID: 15374705
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Stiff-tail or midpiece syndrome].
    Schieferstein G; Wolburg H; Adam W
    Andrologia; 1987; 19(1):5-8. PubMed ID: 3688478
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biallelic variants in
    Martinez G; Beurois J; Dacheux D; Cazin C; Bidart M; Kherraf ZE; Robinson DR; Satre V; Le Gac G; Ka C; Gourlaouen I; Fichou Y; Petre G; Dulioust E; Zouari R; Thierry-Mieg N; Touré A; Arnoult C; Bonhivers M; Ray P; Coutton C
    J Med Genet; 2020 Oct; 57(10):708-716. PubMed ID: 32161152
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.
    Zhang B; Khan I; Liu C; Ma A; Khan A; Zhang Y; Zhang H; Kakakhel MBS; Zhou J; Zhang W; Li Y; Ali A; Jiang X; Murtaza G; Khan R; Zubair M; Yuan L; Khan M; Wang L; Zhang F; Wang X; Ma H; Shi Q
    Clin Genet; 2021 Jan; 99(1):176-186. PubMed ID: 33070343
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.