BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 24228726)

  • 1. Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.
    Farag HG; Froehler S; Oexle K; Ravindran E; Schindler D; Staab T; Huebner A; Kraemer N; Chen W; Kaindl AM
    Orphanet J Rare Dis; 2013 Nov; 8():178. PubMed ID: 24228726
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation.
    Miyamoto T; Akutsu SN; Fukumitsu A; Morino H; Masatsuna Y; Hosoba K; Kawakami H; Yamamoto T; Shimizu K; Ohashi H; Matsuura S
    Hum Mol Genet; 2017 Nov; 26(22):4429-4440. PubMed ID: 28973348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.
    Issa L; Mueller K; Seufert K; Kraemer N; Rosenkotter H; Ninnemann O; Buob M; Kaindl AM; Morris-Rosendahl DJ
    Orphanet J Rare Dis; 2013 Apr; 8():59. PubMed ID: 23587236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations.
    Bhat V; Girimaji SC; Mohan G; Arvinda HR; Singhmar P; Duvvari MR; Kumar A
    Clin Genet; 2011 Dec; 80(6):532-40. PubMed ID: 21496009
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Novel mutations c.28G>T (p.Ala10Ser) and c.189G>T (p.Glu63Asp) in WDR62 associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly type 2.
    Banerjee S; Chen H; Huang H; Wu J; Yang Z; Deng W; Chen D; Deng J; Su Y; Li Y; Wu C; Wang Y; Zeng H; Wang Y; Li X
    Oncotarget; 2016 Nov; 7(48):78363-78371. PubMed ID: 27852057
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability.
    Nardello R; Fontana A; Antona V; Beninati A; Mangano GD; Stallone MC; Mangano S
    Brain Dev; 2018 Jan; 40(1):58-64. PubMed ID: 28756000
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the
    Slezak R; Smigiel R; Obersztyn E; Pollak A; Dawidziuk M; Wiszniewski W; Bekiesinska-Figatowska M; Rydzanicz M; Ploski R; Gawlinski P
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33921653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aurora A phosphorylation of WD40-repeat protein 62 in mitotic spindle regulation.
    Lim NR; Yeap YY; Ang CS; Williamson NA; Bogoyevitch MA; Quinn LM; Ng DC
    Cell Cycle; 2016; 15(3):413-24. PubMed ID: 26713495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.
    Sgourdou P; Mishra-Gorur K; Saotome I; Henagariu O; Tuysuz B; Campos C; Ishigame K; Giannikou K; Quon JL; Sestan N; Caglayan AO; Gunel M; Louvi A
    Sci Rep; 2017 Mar; 7():43708. PubMed ID: 28272472
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WD40-repeat protein 62 is a JNK-phosphorylated spindle pole protein required for spindle maintenance and timely mitotic progression.
    Bogoyevitch MA; Yeap YY; Qu Z; Ngoei KR; Yip YY; Zhao TT; Heng JI; Ng DC
    J Cell Sci; 2012 Nov; 125(Pt 21):5096-109. PubMed ID: 22899712
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development.
    Shohayeb B; Lim NR; Ho U; Xu Z; Dottori M; Quinn L; Ng DCH
    Mol Neurobiol; 2018 Jul; 55(7):5409-5424. PubMed ID: 28940170
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly.
    Kousar R; Hassan MJ; Khan B; Basit S; Mahmood S; Mir A; Ahmad W; Ansar M
    BMC Neurol; 2011 Oct; 11():119. PubMed ID: 21961505
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel WDR62 mutation causes primary microcephaly in a Pakistani family.
    Memon MM; Raza SI; Basit S; Kousar R; Ahmad W; Ansar M
    Mol Biol Rep; 2013 Jan; 40(1):591-5. PubMed ID: 23065275
    [TBL] [Abstract][Full Text] [Related]  

  • 17. WDR62 is associated with the spindle pole and is mutated in human microcephaly.
    Nicholas AK; Khurshid M; Désir J; Carvalho OP; Cox JJ; Thornton G; Kausar R; Ansar M; Ahmad W; Verloes A; Passemard S; Misson JP; Lindsay S; Gergely F; Dobyns WB; Roberts E; Abramowicz M; Woods CG
    Nat Genet; 2010 Nov; 42(11):1010-4. PubMed ID: 20890279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Microcephaly-Associated Protein Wdr62/CG7337 Is Required to Maintain Centrosome Asymmetry in Drosophila Neuroblasts.
    Ramdas Nair A; Singh P; Salvador Garcia D; Rodriguez-Crespo D; Egger B; Cabernard C
    Cell Rep; 2016 Feb; 14(5):1100-1113. PubMed ID: 26804909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size.
    Chen JF; Zhang Y; Wilde J; Hansen KC; Lai F; Niswander L
    Nat Commun; 2014 May; 5():3885. PubMed ID: 24875059
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel compound heterozygous mutations in
    Naseer MI; Rasool M; Abdulkareem AA; Chaudhary AG; Zaidi SK; Al-Qahtani MH
    Pak J Med Sci; 2019; 35(3):764-770. PubMed ID: 31258591
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.