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Journal Abstract Search

318 related items for PubMed ID: 20823249

  • 21. ASPM and citron kinase co-localize to the midbody ring during cytokinesis.
    Paramasivam M, Chang YJ, LoTurco JJ.
    Cell Cycle; 2007 Jul 01; 6(13):1605-12. PubMed ID: 17534152
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  • 25. Loss of Aspm causes increased apoptosis of developing neural cells during mouse cerebral corticogenesis.
    Tonosaki M, Fujimori A, Yaoi T, Itoh K.
    PLoS One; 2023 Jul 01; 18(11):e0294893. PubMed ID: 38019816
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  • 27. Novel Pathogenic Mutation Mapping of ASPM Gene in Consanguineous Pakistani Families with Primary Microcephaly.
    Batool T, Irshad S, Mahmood K.
    Braz J Biol; 2021 Jul 01; 83():e246040. PubMed ID: 34378666
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  • 32. Microtubule minus-end regulation at spindle poles by an ASPM-katanin complex.
    Jiang K, Rezabkova L, Hua S, Liu Q, Capitani G, Altelaar AFM, Heck AJR, Kammerer RA, Steinmetz MO, Akhmanova A.
    Nat Cell Biol; 2017 May 01; 19(5):480-492. PubMed ID: 28436967
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  • 36. 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 01; 42(11):1010-4. PubMed ID: 20890279
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  • 38. A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family.
    Naqvi SF, Shabbir RMK, Tolun A, Basit S, Malik S.
    Genet Test Mol Biomarkers; 2022 Jan 01; 26(1):37-42. PubMed ID: 35089071
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  • 39. A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.
    Hashmi JA, Al-Harbi KM, Ramzan K, Albalawi AM, Mehmood A, Samman MI, Basit S.
    Ann Saudi Med; 2016 Jan 01; 36(6):391-396. PubMed ID: 27920410
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  • 40. CO-OCCURRENCE OF PRIMARY MICROCEPHALY CAUSED BY A NOVEL HOMOZYGOUS ASPM MUTATION ALONG WITH X-LINKED ICHTHYOSIS IN THE SAME PATIENT.
    Abdel-Hamid MS, Ismail MF, Darwish HA, Effat LK, Zaki MS, Abdel-Salam GM.
    Genet Couns; 2016 Jan 01; 27(1):25-33. PubMed ID: 27192889
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