These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

522 related articles for article (PubMed ID: 34862179)

  • 1. Time is of the essence: the molecular mechanisms of primary microcephaly.
    Phan TP; Holland AJ
    Genes Dev; 2021 Dec; 35(23-24):1551-1578. PubMed ID: 34862179
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Centrosome defects cause microcephaly by activating the 53BP1-USP28-TP53 mitotic surveillance pathway.
    Phan TP; Maryniak AL; Boatwright CA; Lee J; Atkins A; Tijhuis A; Spierings DC; Bazzi H; Foijer F; Jordan PW; Stracker TH; Holland AJ
    EMBO J; 2021 Jan; 40(1):e106118. PubMed ID: 33226141
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Same but different: pleiotropy in centrosome-related microcephaly.
    O'Neill RS; Schoborg TA; Rusan NM
    Mol Biol Cell; 2018 Feb; 29(3):241-246. PubMed ID: 29382806
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly.
    Hussain MS; Baig SM; Neumann S; Peche VS; Szczepanski S; Nürnberg G; Tariq M; Jameel M; Khan TN; Fatima A; Malik NA; Ahmad I; Altmüller J; Frommolt P; Thiele H; Höhne W; Yigit G; Wollnik B; Neubauer BA; Nürnberg P; Noegel AA
    Hum Mol Genet; 2013 Dec; 22(25):5199-214. PubMed ID: 23918663
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Small organelle, big responsibility: the role of centrosomes in development and disease.
    Chavali PL; Pütz M; Gergely F
    Philos Trans R Soc Lond B Biol Sci; 2014 Sep; 369(1650):. PubMed ID: 25047622
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nearly complete deletion of BubR1 causes microcephaly through shortened mitosis and massive cell death.
    Simmons AJ; Park R; Sterling NA; Jang MH; van Deursen JMA; Yen TJ; Cho SH; Kim S
    Hum Mol Genet; 2019 Jun; 28(11):1822-1836. PubMed ID: 30668728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Centrosome and the Primary Cilium: The Yin and Yang of a Hybrid Organelle.
    Joukov V; De Nicolo A
    Cells; 2019 Jul; 8(7):. PubMed ID: 31295970
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A unique set of centrosome proteins requires pericentrin for spindle-pole localization and spindle orientation.
    Chen CT; Hehnly H; Yu Q; Farkas D; Zheng G; Redick SD; Hung HF; Samtani R; Jurczyk A; Akbarian S; Wise C; Jackson A; Bober M; Guo Y; Lo C; Doxsey S
    Curr Biol; 2014 Oct; 24(19):2327-2334. PubMed ID: 25220058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Consequences of Centrosome Dysfunction During Brain Development.
    Nano M; Basto R
    Adv Exp Med Biol; 2017; 1002():19-45. PubMed ID: 28600781
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Assays to Study Mitotic Centrosome and Spindle Pole Assembly and Regulation.
    Joukov V; Walter JC; De Nicolo A
    Methods Mol Biol; 2016; 1413():207-35. PubMed ID: 27193852
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cdk5rap2 exposes the centrosomal root of microcephaly syndromes.
    Megraw TL; Sharkey JT; Nowakowski RS
    Trends Cell Biol; 2011 Aug; 21(8):470-80. PubMed ID: 21632253
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic causes of microcephaly and lessons for neuronal development.
    Gilmore EC; Walsh CA
    Wiley Interdiscip Rev Dev Biol; 2013 Jul; 2(4):461-78. PubMed ID: 24014418
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular causes of primary microcephaly and related diseases: a report from the UNIA Workshop.
    Stracker TH; Morrison CG; Gergely F
    Chromosoma; 2020 Jun; 129(2):115-120. PubMed ID: 32424716
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Centrosome regulation and function in mammalian cortical neurogenesis.
    Yang J; Hu X; Ma J; Shi SH
    Curr Opin Neurobiol; 2021 Aug; 69():256-266. PubMed ID: 34303132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA Replication proteins in primary microcephaly syndromes.
    Tingler M; Philipp M; Burkhalter MD
    Biol Cell; 2022 Jun; 114(6):143-159. PubMed ID: 35182397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Centrosomes and the art of mitotic spindle maintenance.
    Hinchcliffe EH
    Int Rev Cell Mol Biol; 2014; 313():179-217. PubMed ID: 25376493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
    Alkuraya FS; Cai X; Emery C; Mochida GH; Al-Dosari MS; Felie JM; Hill RS; Barry BJ; Partlow JN; Gascon GG; Kentab A; Jan M; Shaheen R; Feng Y; Walsh CA
    Am J Hum Genet; 2011 May; 88(5):536-47. PubMed ID: 21529751
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. CCDC57 Cooperates with Microtubules and Microcephaly Protein CEP63 and Regulates Centriole Duplication and Mitotic Progression.
    Gurkaslar HK; Culfa E; Arslanhan MD; Lince-Faria M; Firat-Karalar EN
    Cell Rep; 2020 May; 31(6):107630. PubMed ID: 32402286
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of mitotic kinases in coupling the centrosome cycle with the assembly of the mitotic spindle.
    Wang G; Jiang Q; Zhang C
    J Cell Sci; 2014 Oct; 127(Pt 19):4111-22. PubMed ID: 25128564
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.