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 *

148 related articles for article (PubMed ID: 38019816)

  • 1. 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; 18(11):e0294893. PubMed ID: 38019816
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size.
    Johnson MB; Sun X; Kodani A; Borges-Monroy R; Girskis KM; Ryu SC; Wang PP; Patel K; Gonzalez DM; Woo YM; Yan Z; Liang B; Smith RS; Chatterjee M; Coman D; Papademetris X; Staib LH; Hyder F; Mandeville JB; Grant PE; Im K; Kwak H; Engelhardt JF; Walsh CA; Bae BI
    Nature; 2018 Apr; 556(7701):370-375. PubMed ID: 29643508
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Disruption of Aspm causes microcephaly with abnormal neuronal differentiation.
    Fujimori A; Itoh K; Goto S; Hirakawa H; Wang B; Kokubo T; Kito S; Tsukamoto S; Fushiki S
    Brain Dev; 2014 Sep; 36(8):661-9. PubMed ID: 24220505
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline.
    Pulvers JN; Bryk J; Fish JL; Wilsch-Bräuninger M; Arai Y; Schreier D; Naumann R; Helppi J; Habermann B; Vogt J; Nitsch R; Tóth A; Enard W; Pääbo S; Huttner WB
    Proc Natl Acad Sci U S A; 2010 Sep; 107(38):16595-600. PubMed ID: 20823249
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of abnormal spindle-like, microcephaly-associated (Aspm) disrupts female folliculogenesis in mice during maturation and aging.
    Mori M; Tando S; Ogi H; Tonosaki M; Yaoi T; Fujimori A; Itoh K
    Reprod Biol; 2022 Sep; 22(3):100673. PubMed ID: 35901620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules.
    Gai M; Bianchi FT; Vagnoni C; Vernì F; Bonaccorsi S; Pasquero S; Berto GE; Sgrò F; Chiotto AM; Annaratone L; Sapino A; Bergo A; Landsberger N; Bond J; Huttner WB; Di Cunto F
    EMBO Rep; 2016 Oct; 17(10):1396-1409. PubMed ID: 27562601
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ionizing radiation downregulates ASPM, a gene responsible for microcephaly in humans.
    Fujimori A; Yaoi T; Ogi H; Wang B; Suetomi K; Sekine E; Yu D; Kato T; Takahashi S; Okayasu R; Itoh K; Fushiki S
    Biochem Biophys Res Commun; 2008 May; 369(3):953-7. PubMed ID: 18331833
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ASPM is a major determinant of cerebral cortical size.
    Bond J; Roberts E; Mochida GH; Hampshire DJ; Scott S; Askham JM; Springell K; Mahadevan M; Crow YJ; Markham AF; Walsh CA; Woods CG
    Nat Genet; 2002 Oct; 32(2):316-20. PubMed ID: 12355089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Aspm sustains postnatal cerebellar neurogenesis and medulloblastoma growth in mice.
    Williams SE; Garcia I; Crowther AJ; Li S; Stewart A; Liu H; Lough KJ; O'Neill S; Veleta K; Oyarzabal EA; Merrill JR; Shih YY; Gershon TR
    Development; 2015 Nov; 142(22):3921-32. PubMed ID: 26450969
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory.
    Passemard S; Verloes A; Billette de Villemeur T; Boespflug-Tanguy O; Hernandez K; Laurent M; Isidor B; Alberti C; Pouvreau N; Drunat S; Gérard B; El Ghouzzi V; Gallego J; Elmaleh-Bergès M; Huttner WB; Eliez S; Gressens P; Schaer M
    Cortex; 2016 Jan; 74():158-76. PubMed ID: 26691732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Akirin2 is essential for the formation of the cerebral cortex.
    Bosch PJ; Fuller LC; Sleeth CM; Weiner JA
    Neural Dev; 2016 Nov; 11(1):21. PubMed ID: 27871306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein.
    Kouprina N; Pavlicek A; Collins NK; Nakano M; Noskov VN; Ohzeki J; Mochida GH; Risinger JI; Goldsmith P; Gunsior M; Solomon G; Gersch W; Kim JH; Barrett JC; Walsh CA; Jurka J; Masumoto H; Larionov V
    Hum Mol Genet; 2005 Aug; 14(15):2155-65. PubMed ID: 15972725
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High-mobility group nucleosomal binding domain 2 protects against microcephaly by maintaining global chromatin accessibility during corticogenesis.
    Gao XL; Tian WJ; Liu B; Wu J; Xie W; Shen Q
    J Biol Chem; 2020 Jan; 295(2):468-480. PubMed ID: 31699896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 12(6):. PubMed ID: 36980263
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cenpj Regulates Cilia Disassembly and Neurogenesis in the Developing Mouse Cortex.
    Ding W; Wu Q; Sun L; Pan NC; Wang X
    J Neurosci; 2019 Mar; 39(11):1994-2010. PubMed ID: 30626697
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Longitudinal Diffusion Tensor Imaging Revealed Nerve Fiber Alterations in Aspm Mutated Microcephaly Model Mice.
    Ogi H; Nitta N; Tando S; Fujimori A; Aoki I; Fushiki S; Itoh K
    Neuroscience; 2018 Feb; 371():325-336. PubMed ID: 29253521
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal recessive primary microcephaly due to ASPM mutations: An update.
    Létard P; Drunat S; Vial Y; Duerinckx S; Ernault A; Amram D; Arpin S; Bertoli M; Busa T; Ceulemans B; Desir J; Doco-Fenzy M; Elalaoui SC; Devriendt K; Faivre L; Francannet C; Geneviève D; Gérard M; Gitiaux C; Julia S; Lebon S; Lubala T; Mathieu-Dramard M; Maurey H; Metreau J; Nasserereddine S; Nizon M; Pierquin G; Pouvreau N; Rivier-Ringenbach C; Rossi M; Schaefer E; Sefiani A; Sigaudy S; Sznajer Y; Tunca Y; Guilmin Crepon S; Alberti C; Elmaleh-Bergès M; Benzacken B; Wollnick B; Woods CG; Rauch A; Abramowicz M; El Ghouzzi V; Gressens P; Verloes A; Passemard S
    Hum Mutat; 2018 Mar; 39(3):319-332. PubMed ID: 29243349
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Angelman syndrome protein UBE3A interacts with primary microcephaly protein ASPM, localizes to centrosomes and regulates chromosome segregation.
    Singhmar P; Kumar A
    PLoS One; 2011; 6(5):e20397. PubMed ID: 21633703
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In vivo fate analysis reveals the multipotent and self-renewal features of embryonic AspM expressing cells.
    Marinaro C; Butti E; Bergamaschi A; Papale A; Furlan R; Comi G; Martino G; Muzio L
    PLoS One; 2011 Apr; 6(4):e19419. PubMed ID: 21559369
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Developmental neurogenesis in mouse and Xenopus is impaired in the absence of Nosip.
    Hoffmeister M; Krieg J; Ehrke A; Seigfried FA; Wischmann L; Dietmann P; Kühl SJ; Oess S
    Dev Biol; 2017 Sep; 429(1):200-212. PubMed ID: 28663132
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.