72 related articles for article (PubMed ID: 38576530)
1. Functional analysis of a novel intronic variant of
Luo S; Ren L; Wang R; Hu J; Wei W; Feng Y; Huang S
Heliyon; 2024 May; 10(10):e30285. PubMed ID: 38818167
[TBL] [Abstract][Full Text] [Related]
2. Microcephaly-associated protein WDR62 shuttles from the Golgi apparatus to the spindle poles in human neural progenitors.
Dell'Amico C; Angulo Salavarria MM; Takeo Y; Saotome I; Dell'Anno MT; Galimberti M; Pellegrino E; Cattaneo E; Louvi A; Onorati M
Elife; 2023 Jun; 12():. PubMed ID: 37272619
[TBL] [Abstract][Full Text] [Related]
3. Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disability.
Saima ; Khan A; Ali S; Jiang J; Miao Z; Kamil A; Khan SN; Arold ST
Neurogenetics; 2024 May; ():. PubMed ID: 38795246
[TBL] [Abstract][Full Text] [Related]
4. A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.
Zombor M; Kalmár T; Nagy N; Berényi M; Telcs B; Maróti Z; Brandau O; Sztriha L
J Appl Genet; 2019 May; 60(2):151-162. PubMed ID: 30706430
[TBL] [Abstract][Full Text] [Related]
5. Autosomal recessive primary microcephaly type 2 associated with a novel
Chen H; Zheng Y; Wu H; Cai N; Xu G; Lin Y; Li JJ
Front Neurol; 2024; 15():1341864. PubMed ID: 38576530
[TBL] [Abstract][Full Text] [Related]
6. Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephaly.
Aslam K; Saeed A; Saeed HI; Bashir R; Abid H; Akhtar R; Habib N; Khan R; Asif R; Rafiq S; Asif M; Makhdoom EUH; Hussain MS; Baig SM; Anjum I
Mol Biol Rep; 2024 Jun; 51(1):783. PubMed ID: 38926176
[TBL] [Abstract][Full Text] [Related]
7. Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly.
Aryan H; Zokaei S; Farhud D; Keykhaei M; Ashrafi MR; Rasulinezhad M; Hosseini SMM; Razmara E; Tavasoli AR
Ir J Med Sci; 2022 Dec; 191(6):2733-2741. PubMed ID: 35031939
[TBL] [Abstract][Full Text] [Related]
8. Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in
Bolat H; Sağer SG; Türkyılmaz A; Çebi AH; Akın Y; Onay H; Özkınay F; Ünsel-Bolat G
Mol Syndromol; 2022 Dec; 13(5):363-369. PubMed ID: 36588751
[TBL] [Abstract][Full Text] [Related]
9. A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.
Naseer MI; Rasool M; Sogaty S; Chaudhary RA; Mansour HM; Chaudhary AG; Abuzenadah AM; Al-Qahtani MH
Ann Saudi Med; 2017; 37(2):148-153. PubMed ID: 28377545
[TBL] [Abstract][Full Text] [Related]
10. A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report.
Cherkaoui Jaouad I; Zrhidri A; Jdioui W; Lyahyai J; Raymond L; Egéa G; Taoudi M; El Mouatassim S; Sefiani A
BMC Med Genet; 2018 Jul; 19(1):118. PubMed ID: 30021525
[TBL] [Abstract][Full Text] [Related]
11. The impact of TP53 activation and apoptosis in primary hereditary microcephaly.
Iegiani G; Ferraro A; Pallavicini G; Di Cunto F
Front Neurosci; 2023; 17():1220010. PubMed ID: 37457016
[TBL] [Abstract][Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]