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Journal Abstract Search

472 related items for PubMed ID: 25548773

  • 41. Cdk5rap2 interacts with pericentrin to maintain the neural progenitor pool in the developing neocortex.
    Buchman JJ, Tseng HC, Zhou Y, Frank CL, Xie Z, Tsai LH.
    Neuron; 2010 May 13; 66(3):386-402. PubMed ID: 20471352
    [Abstract] [Full Text] [Related]

  • 42. D40/KNL1/CASC5 and autosomal recessive primary microcephaly.
    Takimoto M.
    Congenit Anom (Kyoto); 2017 Nov 13; 57(6):191-196. PubMed ID: 28901661
    [Abstract] [Full Text] [Related]

  • 43. A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.
    Hussain MS, Baig SM, Neumann S, Nürnberg G, Farooq M, Ahmad I, Alef T, Hennies HC, Technau M, Altmüller J, Frommolt P, Thiele H, Noegel AA, Nürnberg P.
    Am J Hum Genet; 2012 May 04; 90(5):871-8. PubMed ID: 22521416
    [Abstract] [Full Text] [Related]

  • 44. Genetic interaction between PLK1 and downstream MCPH proteins in the control of centrosome asymmetry and cell fate during neural progenitor division.
    González-Martínez J, Cwetsch AW, Gilabert-Juan J, Gómez J, Garaulet G, Schneider P, de Cárcer G, Mulero F, Caleiras E, Megías D, Porlan E, Malumbres M.
    Cell Death Differ; 2022 Aug 04; 29(8):1474-1485. PubMed ID: 35058575
    [Abstract] [Full Text] [Related]

  • 45. 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 18; 19(1):118. PubMed ID: 30021525
    [Abstract] [Full Text] [Related]

  • 46. 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 18; 42(11):1010-4. PubMed ID: 20890279
    [Abstract] [Full Text] [Related]

  • 47. The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis.
    Zhou X, Zhi Y, Yu J, Xu D.
    Int J Mol Sci; 2020 Mar 01; 21(5):. PubMed ID: 32121580
    [Abstract] [Full Text] [Related]

  • 48. The Multiple Mitotic Roles of the ASPM Orthologous Proteins: Insight into the Etiology of ASPM-Dependent Microcephaly.
    Razuvaeva AV, Graziadio L, Palumbo V, Pavlova GA, Popova JV, Pindyurin AV, Bonaccorsi S, Somma MP, Gatti M.
    Cells; 2023 Mar 16; 12(6):. PubMed ID: 36980263
    [Abstract] [Full Text] [Related]

  • 49. Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum.
    Mahmood S, Ahmad W, Hassan MJ.
    Orphanet J Rare Dis; 2011 Jun 13; 6():39. PubMed ID: 21668957
    [Abstract] [Full Text] [Related]

  • 50. Mutations of KIF14 cause primary microcephaly by impairing cytokinesis.
    Moawia A, Shaheen R, Rasool S, Waseem SS, Ewida N, Budde B, Kawalia A, Motameny S, Khan K, Fatima A, Jameel M, Ullah F, Akram T, Ali Z, Abdullah U, Irshad S, Höhne W, Noegel AA, Al-Owain M, Hörtnagel K, Stöbe P, Baig SM, Nürnberg P, Alkuraya FS, Hahn A, Hussain MS.
    Ann Neurol; 2017 Oct 13; 82(4):562-577. PubMed ID: 28892560
    [Abstract] [Full Text] [Related]

  • 51. Deficient adaptation to centrosome duplication defects in neural progenitors causes microcephaly and subcortical heterotopias.
    González-Martínez J, Cwetsch AW, Martínez-Alonso D, López-Sainz LR, Almagro J, Melati A, Gómez J, Pérez-Martínez M, Megías D, Boskovic J, Gilabert-Juan J, Graña-Castro O, Pierani A, Behrens A, Ortega S, Malumbres M.
    JCI Insight; 2021 Aug 23; 6(16):. PubMed ID: 34237032
    [Abstract] [Full Text] [Related]

  • 52. Microcephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression.
    Novorol C, Burkhardt J, Wood KJ, Iqbal A, Roque C, Coutts N, Almeida AD, He J, Wilkinson CJ, Harris WA.
    Open Biol; 2013 Oct 23; 3(10):130065. PubMed ID: 24153002
    [Abstract] [Full Text] [Related]

  • 53. A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.
    Darvish H, Esmaeeli-Nieh S, Monajemi GB, Mohseni M, Ghasemi-Firouzabadi S, Abedini SS, Bahman I, Jamali P, Azimi S, Mojahedi F, Dehghan A, Shafeghati Y, Jankhah A, Falah M, Soltani Banavandi MJ, Ghani M, Garshasbi M, Rakhshani F, Naghavi A, Tzschach A, Neitzel H, Ropers HH, Kuss AW, Behjati F, Kahrizi K, Najmabadi H.
    J Med Genet; 2010 Dec 23; 47(12):823-8. PubMed ID: 20978018
    [Abstract] [Full Text] [Related]

  • 54. Molecular genetics of human primary microcephaly: an overview.
    Faheem M, Naseer MI, Rasool M, Chaudhary AG, Kumosani TA, Ilyas AM, Pushparaj P, Ahmed F, Algahtani HA, Al-Qahtani MH, Saleh Jamal H.
    BMC Med Genomics; 2015 Dec 23; 8 Suppl 1(Suppl 1):S4. PubMed ID: 25951892
    [Abstract] [Full Text] [Related]

  • 55. Misregulated chromosome condensation in MCPH1 primary microcephaly is mediated by condensin II.
    Trimborn M, Schindler D, Neitzel H, Hirano T.
    Cell Cycle; 2006 Feb 23; 5(3):322-6. PubMed ID: 16434882
    [Abstract] [Full Text] [Related]

  • 56. The Genetics of Primary Microcephaly.
    Jayaraman D, Bae BI, Walsh CA.
    Annu Rev Genomics Hum Genet; 2018 Aug 31; 19():177-200. PubMed ID: 29799801
    [Abstract] [Full Text] [Related]

  • 57. 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 29; 7(48):78363-78371. PubMed ID: 27852057
    [Abstract] [Full Text] [Related]

  • 58. The centrosome duplication cycle in health and disease.
    Nigg EA, Čajánek L, Arquint C.
    FEBS Lett; 2014 Aug 01; 588(15):2366-72. PubMed ID: 24951839
    [Abstract] [Full Text] [Related]

  • 59. Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome.
    McIntyre RE, Lakshminarasimhan Chavali P, Ismail O, Carragher DM, Sanchez-Andrade G, Forment JV, Fu B, Del Castillo Velasco-Herrera M, Edwards A, van der Weyden L, Yang F, Sanger Mouse Genetics Project, Ramirez-Solis R, Estabel J, Gallagher FA, Logan DW, Arends MJ, Tsang SH, Mahajan VB, Scudamore CL, White JK, Jackson SP, Gergely F, Adams DJ.
    PLoS Genet; 2012 Aug 01; 8(11):e1003022. PubMed ID: 23166506
    [Abstract] [Full Text] [Related]

  • 60. A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family.
    Abdullah U, Farooq M, Mang Y, Marriam Bakhtiar S, Fatima A, Hansen L, Kjaer KW, Larsen LA, Faryal S, Tommerup N, Mahmood Baig S.
    Eur J Med Genet; 2017 Dec 01; 60(12):627-630. PubMed ID: 28778786
    [Abstract] [Full Text] [Related]

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