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 *

105 related articles for article (PubMed ID: 26903504)

  • 1. Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis.
    Breuss M; Fritz T; Gstrein T; Chan K; Ushakova L; Yu N; Vonberg FW; Werner B; Elling U; Keays DA
    Development; 2016 Apr; 143(7):1126-33. PubMed ID: 26903504
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
    Breuss M; Heng JI; Poirier K; Tian G; Jaglin XH; Qu Z; Braun A; Gstrein T; Ngo L; Haas M; Bahi-Buisson N; Moutard ML; Passemard S; Verloes A; Gressens P; Xie Y; Robson KJ; Rani DS; Thangaraj K; Clausen T; Chelly J; Cowan NJ; Keays DA
    Cell Rep; 2012 Dec; 2(6):1554-62. PubMed ID: 23246003
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition.
    Breuss MW; Hansen AH; Landler L; Keays DA
    Behav Brain Res; 2017 Apr; 323():47-55. PubMed ID: 28130172
    [TBL] [Abstract][Full Text] [Related]  

  • 4. p53 deletion rescues lethal microcephaly in a mouse model with neural stem cell abscission defects.
    Little JN; Dwyer ND
    Hum Mol Genet; 2019 Feb; 28(3):434-447. PubMed ID: 30304535
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Minor spliceosome inactivation causes microcephaly, owing to cell cycle defects and death of self-amplifying radial glial cells.
    Baumgartner M; Olthof AM; Aquino GS; Hyatt KC; Lemoine C; Drake K; Sturrock N; Nguyen N; Al Seesi S; Kanadia RN
    Development; 2018 Aug; 145(17):. PubMed ID: 30093551
    [TBL] [Abstract][Full Text] [Related]  

  • 6. TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.
    Ngo L; Haas M; Qu Z; Li SS; Zenker J; Teng KS; Gunnersen JM; Breuss M; Habgood M; Keays DA; Heng JI
    Hum Mol Genet; 2014 Oct; 23(19):5147-58. PubMed ID: 24833723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Augmin deficiency in neural stem cells causes p53-dependent apoptosis and aborts brain development.
    Viais R; Fariña-Mosquera M; Villamor-Payà M; Watanabe S; Palenzuela L; Lacasa C; Lüders J
    Elife; 2021 Aug; 10():. PubMed ID: 34427181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations.
    Madrigal I; Rabionet R; Alvarez-Mora MI; Sanchez A; Rodríguez-Revenga L; Estivill X; Mila M
    Gene; 2019 May; 695():12-17. PubMed ID: 30738969
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Robust elimination of genome-damaged cells safeguards against brain somatic aneuploidy following Knl1 deletion.
    Shi L; Qalieh A; Lam MM; Keil JM; Kwan KY
    Nat Commun; 2019 Jun; 10(1):2588. PubMed ID: 31197172
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly.
    Ghouzzi VE; Bianchi FT; Molineris I; Mounce BC; Berto GE; Rak M; Lebon S; Aubry L; Tocco C; Gai M; Chiotto AM; Sgrò F; Pallavicini G; Simon-Loriere E; Passemard S; Vignuzzi M; Gressens P; Di Cunto F
    Cell Death Dis; 2016 Oct; 7(10):e2440. PubMed ID: 27787521
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 6(16):. PubMed ID: 34237032
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
    Bahi-Buisson N; Poirier K; Fourniol F; Saillour Y; Valence S; Lebrun N; Hully M; Bianco CF; Boddaert N; Elie C; Lascelles K; Souville I; ; Beldjord C; Chelly J
    Brain; 2014 Jun; 137(Pt 6):1676-700. PubMed ID: 24860126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Epistatic interactions between NMD and TRP53 control progenitor cell maintenance and brain size.
    Lin L; Zhao J; Kubota N; Li Z; Lam YL; Nguyen LP; Yang L; Pokharel SP; Blue SM; Yee BA; Chen R; Yeo GW; Chen CW; Chen L; Zheng S
    Neuron; 2024 Jul; 112(13):2157-2176.e12. PubMed ID: 38697111
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trp53 ablation fails to prevent microcephaly in mouse pallium with impaired minor intron splicing.
    White AK; Baumgartner M; Lee MF; Drake KD; Aquino GS; Kanadia RN
    Development; 2021 Oct; 148(20):. PubMed ID: 34557915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Entosis implicates a new role for P53 in microcephaly pathogenesis, beyond apoptosis.
    Sterling NA; Cho SH; Kim S
    Bioessays; 2024 Aug; 46(8):e2300245. PubMed ID: 38778437
    [TBL] [Abstract][Full Text] [Related]  

  • 16. In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells.
    Ito H; Shiwaku H; Yoshida C; Homma H; Luo H; Chen X; Fujita K; Musante L; Fischer U; Frints SG; Romano C; Ikeuchi Y; Shimamura T; Imoto S; Miyano S; Muramatsu SI; Kawauchi T; Hoshino M; Sudol M; Arumughan A; Wanker EE; Rich T; Schwartz C; Matsuzaki F; Bonni A; Kalscheuer VM; Okazawa H
    Mol Psychiatry; 2015 Apr; 20(4):459-71. PubMed ID: 25070536
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.
    Mitani T; Punetha J; Akalin I; Pehlivan D; Dawidziuk M; Coban Akdemir Z; Yilmaz S; Aslan E; Hunter JV; Hijazi H; Grochowski CM; Jhangiani SN; Karaca E; Fatih JM; Iwanowski P; Gambin T; Wlasienko P; Goszczanska-Ciuchta A; Bekiesinska-Figatowska M; Hosseini M; Arzhangi S; Najmabadi H; Rosenfeld JA; Du H; Marafi D; Blaser S; Teitelbaum R; Silver R; ; Posey JE; Ropers HH; Gibbs RA; Wiszniewski W; Lupski JR; Chitayat D; Kahrizi K; Gawlinski P
    Am J Hum Genet; 2019 Nov; 105(5):1005-1015. PubMed ID: 31630790
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.