140 related articles for article (PubMed ID: 34569065)
21. Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia.
Tang D; Sha Y; Gao Y; Zhang J; Cheng H; Zhang J; Ni X; Wang C; Xu C; Geng H; He X; Cao Y
Reprod Biol Endocrinol; 2021 Feb; 19(1):27. PubMed ID: 33610189
[TBL] [Abstract][Full Text] [Related]
22. Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells.
Funk MC; Bera AN; Menchen T; Kuales G; Thriene K; Lienkamp SS; Dengjel J; Omran H; Frank M; Arnold SJ
EMBO J; 2015 Apr; 34(8):1078-89. PubMed ID: 25712475
[TBL] [Abstract][Full Text] [Related]
23. Constitutive Cyclin O deficiency results in penetrant hydrocephalus, impaired growth and infertility.
Núnez-Ollé M; Jung C; Terré B; Balsiger NA; Plata C; Roset R; Pardo-Pastor C; Garrido M; Rojas S; Alameda F; Lloreta J; Martín-Caballero J; Flores JM; Stracker TH; Valverde MA; Muñoz FJ; Gil-Gómez G
Oncotarget; 2017 Nov; 8(59):99261-99273. PubMed ID: 29245899
[TBL] [Abstract][Full Text] [Related]
24. Mutations in TP73 cause impaired mucociliary clearance and lissencephaly.
Wallmeier J; Bracht D; Alsaif HS; Dougherty GW; Olbrich H; Cindric S; Dzietko M; Heyer C; Teig N; Thiels C; Faqeih E; Al-Hashim A; Khan S; Mogarri I; Almannai M; Al Otaibi W; Alkuraya FS; Koerner-Rettberg C; Omran H
Am J Hum Genet; 2021 Jul; 108(7):1318-1329. PubMed ID: 34077761
[TBL] [Abstract][Full Text] [Related]
25.
Lu H; Anujan P; Zhou F; Zhang Y; Chong YL; Bingle CD; Roy S
Development; 2019 Mar; 146(6):. PubMed ID: 30877126
[TBL] [Abstract][Full Text] [Related]
26. Mcidas and GemC1 are key regulators for the generation of multiciliated ependymal cells in the adult neurogenic niche.
Kyrousi C; Arbi M; Pilz GA; Pefani DE; Lalioti ME; Ninkovic J; Götz M; Lygerou Z; Taraviras S
Development; 2015 Nov; 142(21):3661-74. PubMed ID: 26395491
[TBL] [Abstract][Full Text] [Related]
27. Novel WEE2 gene variants identified in patients with fertilization failure and female infertility.
Zhao S; Chen T; Yu M; Bian Y; Cao Y; Ning Y; Su S; Zhang J; Zhao S
Fertil Steril; 2019 Mar; 111(3):519-526. PubMed ID: 30827524
[TBL] [Abstract][Full Text] [Related]
28. Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection.
Wambergue C; Zouari R; Fourati Ben Mustapha S; Martinez G; Devillard F; Hennebicq S; Satre V; Brouillet S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Amblard F; Arnoult C; Ray PF; Coutton C
Hum Reprod; 2016 Jun; 31(6):1164-72. PubMed ID: 27094479
[TBL] [Abstract][Full Text] [Related]
29. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene.
Dahlmann J; Sahabian A; Drick N; Haase A; Göhring G; Lachmann N; Ringshausen FC; Welte T; Martin U; Olmer R
Stem Cell Res; 2020 Jul; 46():101850. PubMed ID: 32464346
[TBL] [Abstract][Full Text] [Related]
30. The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient.
Li Y; Jiang C; Zhang X; Liu M; Sun Y; Yang Y; Shen Y
J Assist Reprod Genet; 2021 Mar; 38(3):689-696. PubMed ID: 33403504
[TBL] [Abstract][Full Text] [Related]
31. Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.
Olbrich H; Schmidts M; Werner C; Onoufriadis A; Loges NT; Raidt J; Banki NF; Shoemark A; Burgoyne T; Al Turki S; Hurles ME; ; Köhler G; Schroeder J; Nürnberg G; Nürnberg P; Chung EM; Reinhardt R; Marthin JK; Nielsen KG; Mitchison HM; Omran H
Am J Hum Genet; 2012 Oct; 91(4):672-84. PubMed ID: 23022101
[TBL] [Abstract][Full Text] [Related]
32. Homozygous mutations in
Liu C; Lv M; He X; Zhu Y; Amiri-Yekta A; Li W; Wu H; Kherraf ZE; Liu W; Zhang J; Tan Q; Tang S; Zhu YJ; Zhong Y; Li C; Tian S; Zhang Z; Jin L; Ray P; Zhang F; Cao Y
J Med Genet; 2020 Jan; 57(1):31-37. PubMed ID: 31048344
[TBL] [Abstract][Full Text] [Related]
33. Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.
Guo T; Tu CF; Yang DH; Ding SZ; Lei C; Wang RC; Liu L; Kang X; Shen XQ; Yang YF; Tan ZP; Tan YQ; Luo H
Hum Genet; 2021 May; 140(5):761-773. PubMed ID: 33389130
[TBL] [Abstract][Full Text] [Related]
34. Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
Liu R; Yan Z; Fan Y; Qu R; Chen B; Li B; Wu L; Wu H; Mu J; Zhao L; Wang W; Dong J; Zeng Y; Li Q; Wang L; Sang Q; Zhang Z; Kuang Y
Hum Reprod; 2022 Jun; 37(7):1394-1405. PubMed ID: 35551387
[TBL] [Abstract][Full Text] [Related]
35. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.
Wang Y; Tu C; Nie H; Meng L; Li D; Wang W; Zhang H; Lu G; Lin G; Tan YQ; Du J
J Assist Reprod Genet; 2020 Apr; 37(4):811-820. PubMed ID: 32170493
[TBL] [Abstract][Full Text] [Related]
36. CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia.
Liu L; Zhou K; Song Y; Liu X
Medicine (Baltimore); 2021 Dec; 100(51):e28275. PubMed ID: 34941110
[TBL] [Abstract][Full Text] [Related]
37. Point-of-care whole-exome sequencing of idiopathic male infertility.
Fakhro KA; Elbardisi H; Arafa M; Robay A; Rodriguez-Flores JL; Al-Shakaki A; Syed N; Mezey JG; Abi Khalil C; Malek JA; Al-Ansari A; Al Said S; Crystal RG
Genet Med; 2018 Nov; 20(11):1365-1373. PubMed ID: 29790874
[TBL] [Abstract][Full Text] [Related]
38. Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.
Knowles MR; Ostrowski LE; Leigh MW; Sears PR; Davis SD; Wolf WE; Hazucha MJ; Carson JL; Olivier KN; Sagel SD; Rosenfeld M; Ferkol TW; Dell SD; Milla CE; Randell SH; Yin W; Sannuti A; Metjian HM; Noone PG; Noone PJ; Olson CA; Patrone MV; Dang H; Lee HS; Hurd TW; Gee HY; Otto EA; Halbritter J; Kohl S; Kircher M; Krischer J; Bamshad MJ; Nickerson DA; Hildebrandt F; Shendure J; Zariwala MA
Am J Respir Crit Care Med; 2014 Mar; 189(6):707-17. PubMed ID: 24568568
[TBL] [Abstract][Full Text] [Related]
39. Clinical and genetic analysis of patients with primary ciliary dyskinesia caused by novel DNAAF3 mutations.
Guo Z; Chen W; Huang J; Wang L; Qian L
J Hum Genet; 2019 Aug; 64(8):711-719. PubMed ID: 31186518
[TBL] [Abstract][Full Text] [Related]
40. A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder.
Casey JP; Goggin P; McDaid J; White M; Ennis S; Betts DR; Lucas JS; Elnazir B; Lynch SA
BMC Med Genet; 2015 Jun; 16():45. PubMed ID: 26123568
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
