BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 35218524)

  • 1. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development.
    Accogli A; Lu S; Musante I; Scudieri P; Rosenfeld JA; Severino M; Baldassari S; Iacomino M; Riva A; Balagura G; Piccolo G; Minetti C; Roberto D; Xia F; Razak R; Lawrence E; Hussein M; Chang EY; Holick M; Calì E; Aliberto E; De-Sarro R; Gambardella A; Network UD; Group SS; Emrick L; McCaffery PJA; Clagett-Dame M; Marcogliese PC; Bellen HJ; Lalani SR; Zara F; Striano P; Salpietro V
    Cerebellum; 2023 Apr; 22(2):206-222. PubMed ID: 35218524
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nav2 hypomorphic mutant mice are ataxic and exhibit abnormalities in cerebellar development.
    McNeill EM; Klöckner-Bormann M; Roesler EC; Talton LE; Moechars D; Clagett-Dame M
    Dev Biol; 2011 May; 353(2):331-43. PubMed ID: 21419114
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression pattern of Nav2 in the murine CNS with development.
    Pook C; Ahrens JM; Clagett-Dame M
    Gene Expr Patterns; 2020 Jan; 35():119099. PubMed ID: 32081718
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The atRA-responsive gene neuron navigator 2 functions in neurite outgrowth and axonal elongation.
    Muley PD; McNeill EM; Marzinke MA; Knobel KM; Barr MM; Clagett-Dame M
    Dev Neurobiol; 2008 Nov; 68(13):1441-53. PubMed ID: 18726912
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolated Unilateral Cerebellar Hemispheric Dysplasia: A Rare Entity.
    Chatur C; Balani A; Vadapalli R; Murthy MG
    Can J Neurol Sci; 2019 Nov; 46(6):760-761. PubMed ID: 31352912
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 14-3-3ε and NAV2 interact to regulate neurite outgrowth and axon elongation.
    Marzinke MA; Mavencamp T; Duratinsky J; Clagett-Dame M
    Arch Biochem Biophys; 2013 Dec; 540(1-2):94-100. PubMed ID: 24161943
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MAST1 variant causes mega-corpus-callosum syndrome with cortical malformations but without cerebellar hypoplasia.
    Rodríguez-García ME; Cotrina-Vinagre FJ; Gómez-Cano MLÁ; Martínez de Aragón A; Martín-Hernández E; Martínez-Azorín F
    Am J Med Genet A; 2020 Jun; 182(6):1483-1490. PubMed ID: 32198973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
    Ivanova EL; Mau-Them FT; Riazuddin S; Kahrizi K; Laugel V; Schaefer E; de Saint Martin A; Runge K; Iqbal Z; Spitz MA; Laura M; Drouot N; Gérard B; Deleuze JF; de Brouwer APM; Razzaq A; Dollfus H; Assir MZ; Nitchké P; Hinckelmann MV; Ropers H; Riazuddin S; Najmabadi H; van Bokhoven H; Chelly J
    Am J Hum Genet; 2017 Sep; 101(3):428-440. PubMed ID: 28823707
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy.
    Evers C; Kaufmann L; Seitz A; Paramasivam N; Granzow M; Karch S; Fischer C; Hinderhofer K; Gdynia G; Elsässer M; Pinkert S; Schlesner M; Bartram CR; Moog U
    Am J Med Genet A; 2016 Jun; 170(6):1502-9. PubMed ID: 27016154
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neuron navigator 2 overexpression indicates poor prognosis of colorectal cancer and promotes invasion through the SSH1L/cofilin-1 pathway.
    Tan F; Zhu H; Tao Y; Yu N; Pei Q; Liu H; Zhou Y; Xu H; Song X; Li Y; Zhou Z; He X; Zhang X; Pei H
    J Exp Clin Cancer Res; 2015 Oct; 34():117. PubMed ID: 26452645
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genetic variant in the MAST1 gene is associated with mega-corpus-callosum syndrome with hypoplastic cerebellar vermis, in a fetus.
    Yi S; Tang X; Chen F; Wang L; Chen J; Yang Z; Huang M; Yi S; Huang L; Yang Q; Yang S; Pan P; Qin Z; Luo J
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2358. PubMed ID: 38284444
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The NAV2 homolog Sickie regulates F-actin-mediated axonal growth in Drosophila mushroom body neurons via the non-canonical Rac-Cofilin pathway.
    Abe T; Yamazaki D; Murakami S; Hiroi M; Nitta Y; Maeyama Y; Tabata T
    Development; 2014 Dec; 141(24):4716-28. PubMed ID: 25411210
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities.
    Jeanne M; Demory H; Moutal A; Vuillaume ML; Blesson S; Thépault RA; Marouillat S; Halewa J; Maas SM; Motazacker MM; Mancini GMS; van Slegtenhorst MA; Andreou A; Cox H; Vogt J; Laufman J; Kostandyan N; Babikyan D; Hancarova M; Bendova S; Sedlacek Z; Aldinger KA; Sherr EH; Argilli E; England EM; Audebert-Bellanger S; Bonneau D; Colin E; Denommé-Pichon AS; Gilbert-Dussardier B; Isidor B; Küry S; Odent S; Redon R; Khanna R; Dobyns WB; Bézieau S; Honnorat J; Lohkamp B; Toutain A; Laumonnier F
    Am J Hum Genet; 2021 May; 108(5):951-961. PubMed ID: 33894126
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nav2 is necessary for cranial nerve development and blood pressure regulation.
    McNeill EM; Roos KP; Moechars D; Clagett-Dame M
    Neural Dev; 2010 Feb; 5():6. PubMed ID: 20184720
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of novel genes including
    Weiss B; Ott T; Vick P; Lui JC; Roeth R; Vogel S; Waldmüller S; Hoffmann S; Baron J; Wit JM; Rappold GA
    Front Endocrinol (Lausanne); 2023; 14():1258313. PubMed ID: 38152138
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.
    Whittaker DE; Kasah S; Donovan APA; Ellegood J; Riegman KLH; Volk HA; McGonnell I; Lerch JP; Basson MA
    Am J Med Genet C Semin Med Genet; 2017 Dec; 175(4):n/a. PubMed ID: 29168327
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cerebellar hypoplasia in mice lacking selenoprotein biosynthesis in neurons.
    Wirth EK; Bharathi BS; Hatfield D; Conrad M; Brielmeier M; Schweizer U
    Biol Trace Elem Res; 2014 May; 158(2):203-10. PubMed ID: 24599700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss-of-function mutation of c-Ret causes cerebellar hypoplasia in mice with Hirschsprung disease and Down's syndrome.
    Ohgami N; Iizuka A; Hirai H; Yajima I; Iida M; Shimada A; Tsuzuki T; Jijiwa M; Asai N; Takahashi M; Kato M
    J Biol Chem; 2021; 296():100389. PubMed ID: 33561442
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of CHD8 in cerebellar granule neuron progenitors leads to severe cerebellar hypoplasia, ataxia, and psychiatric behavior in mice.
    Chen X; Chen T; Dong C; Chen H; Dong X; Yang L; Hu L; Wang H; Wu B; Yao Y; Xiong Y; Xiong M; Lin Y; Zhou W
    J Genet Genomics; 2022 Sep; 49(9):859-869. PubMed ID: 35231638
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?
    Laugwitz L; Buchert R; Groeschel S; Riess A; Grimmel M; Beck-Wödl S; Sturm M; Gohla G; Döbler-Neumann M; Krägeloh-Mann I; Haack TB
    Eur J Med Genet; 2020 Jul; 63(7):103938. PubMed ID: 32360255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.