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 *

122 related articles for article (PubMed ID: 37205596)

  • 1. Isolated loss of the AUTS2 long isoform, brain-wide or targeted to
    Song Y; Seward CH; Chen CY; LeBlanc A; Leddy AM; Stubbs L
    bioRxiv; 2023 May; ():. PubMed ID: 37205596
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolated loss of the AUTS2 long isoform, brain-wide or targeted to Calbindin-lineage cells, generates a specific suite of brain, behavioral, and molecular pathologies.
    Song Y; Seward CH; Chen CY; LeBlanc A; Leddy AM; Stubbs L
    Genetics; 2024 Jan; 226(1):. PubMed ID: 37816306
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Mouse Mutation That Dysregulates Neighboring
    Weisner PA; Chen CY; Sun Y; Yoo J; Kao WC; Zhang H; Baltz ET; Troy JM; Stubbs L
    G3 (Bethesda); 2019 Nov; 9(11):3891-3906. PubMed ID: 31554716
    [No Abstract]   [Full Text] [Related]  

  • 4. De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects.
    Martinez-Delgado B; Lopez-Martin E; Lara-Herguedas J; Monzon S; Cuesta I; Juliá M; Aquino V; Rodriguez-Martin C; Damian A; Gonzalo I; Gomez-Mariano G; Baladron B; Cazorla R; Iglesias G; Roman E; Ros P; Tutor P; Mellor S; Jimenez C; Cabrejas MJ; Gonzalez-Vioque E; Alonso J; Bermejo-Sánchez E; Posada M
    Am J Med Genet A; 2021 Mar; 185(3):877-883. PubMed ID: 33346930
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Attention Deficit Hyperactivity and Autism Spectrum Disorders as the Core Symptoms of AUTS2 Syndrome: Description of Five New Patients and Update of the Frequency of Manifestations and Genotype-Phenotype Correlation.
    Sanchez-Jimeno C; Blanco-Kelly F; López-Grondona F; Losada-Del Pozo R; Moreno B; Rodrigo-Moreno M; Martinez-Cayuelas E; Riveiro-Alvarez R; Fenollar-Cortés M; Ayuso C; Rodríguez de Alba M; Lorda-Sanchez I; Almoguera B
    Genes (Basel); 2021 Aug; 12(9):. PubMed ID: 34573342
    [TBL] [Abstract][Full Text] [Related]  

  • 6. AUTS2 isoforms control neuronal differentiation.
    Monderer-Rothkoff G; Tal N; Risman M; Shani O; Nissim-Rafinia M; Malki-Feldman L; Medvedeva V; Groszer M; Meshorer E; Shifman S
    Mol Psychiatry; 2021 Feb; 26(2):666-681. PubMed ID: 30953002
    [TBL] [Abstract][Full Text] [Related]  

  • 7. AUTS2 Regulates RNA Metabolism and Dentate Gyrus Development in Mice.
    Castanza AS; Ramirez S; Tripathi PP; Daza RAM; Kalume FK; Ramirez JM; Hevner RF
    Cereb Cortex; 2021 Aug; 31(10):4808-4824. PubMed ID: 34013328
    [TBL] [Abstract][Full Text] [Related]  

  • 8. AUTS2 Syndrome: Molecular Mechanisms and Model Systems.
    Biel A; Castanza AS; Rutherford R; Fair SR; Chifamba L; Wester JC; Hester ME; Hevner RF
    Front Mol Neurosci; 2022; 15():858582. PubMed ID: 35431798
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
    Beunders G; Voorhoeve E; Golzio C; Pardo LM; Rosenfeld JA; Talkowski ME; Simonic I; Lionel AC; Vergult S; Pyatt RE; van de Kamp J; Nieuwint A; Weiss MM; Rizzu P; Verwer LE; van Spaendonk RM; Shen Y; Wu BL; Yu T; Yu Y; Chiang C; Gusella JF; Lindgren AM; Morton CC; van Binsbergen E; Bulk S; van Rossem E; Vanakker O; Armstrong R; Park SM; Greenhalgh L; Maye U; Neill NJ; Abbott KM; Sell S; Ladda R; Farber DM; Bader PI; Cushing T; Drautz JM; Konczal L; Nash P; de Los Reyes E; Carter MT; Hopkins E; Marshall CR; Osborne LR; Gripp KW; Thrush DL; Hashimoto S; Gastier-Foster JM; Astbury C; Ylstra B; Meijers-Heijboer H; Posthuma D; Menten B; Mortier G; Scherer SW; Eichler EE; Girirajan S; Katsanis N; Groffen AJ; Sistermans EA
    Am J Hum Genet; 2013 Feb; 92(2):210-20. PubMed ID: 23332918
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders.
    Pang W; Yi X; Li L; Liu L; Xiang W; Xiao L
    Front Psychiatry; 2021; 12():580433. PubMed ID: 33967843
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transcriptional Complexity and Distinct Expression Patterns of
    Kondrychyn I; Robra L; Thirumalai V
    G3 (Bethesda); 2017 Aug; 7(8):2577-2593. PubMed ID: 28626003
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in
    Pauli S; Berger H; Ufartes R; Borchers A
    Front Cell Dev Biol; 2021; 9():779009. PubMed ID: 34805182
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Merdrignac C; Clément AE; Montfort J; Murat F; Bobe J
    Cells; 2022 Aug; 11(17):. PubMed ID: 36078102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Auts2 enhances neurogenesis and promotes expansion of the cerebral cortex.
    Boucherie C; Alkailani M; Jossin Y; Ruiz-Reig N; Mahdi A; Aldaalis A; Aittaleb M; Tissir F
    J Adv Res; 2024 Jul; ():. PubMed ID: 39013538
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterozygous Disruption of Autism susceptibility candidate 2 Causes Impaired Emotional Control and Cognitive Memory.
    Hori K; Nagai T; Shan W; Sakamoto A; Abe M; Yamazaki M; Sakimura K; Yamada K; Hoshino M
    PLoS One; 2015; 10(12):e0145979. PubMed ID: 26717414
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
    Beunders G; van de Kamp J; Vasudevan P; Morton J; Smets K; Kleefstra T; de Munnik SA; Schuurs-Hoeijmakers J; Ceulemans B; Zollino M; Hoffjan S; Wieczorek S; So J; Mercer L; Walker T; Velsher L; ; Parker MJ; Magee AC; Elffers B; Kooy RF; Yntema HG; Meijers-Heijboer EJ; Sistermans EA
    J Med Genet; 2016 Aug; 53(8):523-32. PubMed ID: 27075013
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms.
    Patowary A; Zhang P; Jops C; Vuong CK; Ge X; Hou K; Kim M; Gong N; Margolis M; Vo D; Wang X; Liu C; Pasaniuc B; Li JJ; Gandal MJ; de la Torre-Ubieta L
    bioRxiv; 2023 Oct; ():. PubMed ID: 36993726
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability.
    Fan Y; Qiu W; Wang L; Gu X; Yu Y
    Am J Med Genet A; 2016 Feb; 170A(2):515-522. PubMed ID: 26545289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AUTS2 Governs Cerebellar Development, Purkinje Cell Maturation, Motor Function and Social Communication.
    Yamashiro K; Hori K; Lai ESK; Aoki R; Shimaoka K; Arimura N; Egusa SF; Sakamoto A; Abe M; Sakimura K; Watanabe T; Uesaka N; Kano M; Hoshino M
    iScience; 2020 Dec; 23(12):101820. PubMed ID: 33305180
    [No Abstract]   [Full Text] [Related]  

  • 20. Activity-Dependent Differential Regulation of Auts2 Isoforms In Vitro and In Vivo.
    Pang W; Wang M; Bi Q; Li H; Zhou Q; Ye X; Xiang W; Xiao L
    Mol Neurobiol; 2023 Jun; 60(6):2973-2985. PubMed ID: 36754912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.