BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 34487988)

  • 1. Rare NRXN1 missense variants identified in autism interfered protein degradation and Drosophila sleeping.
    Liu Y; Shen L; Zhang Y; Zhao R; Liu C; Luo S; Chen J; Xia L; Li T; Peng Y; Xia K
    J Psychiatr Res; 2021 Nov; 143():113-122. PubMed ID: 34487988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
    Ishizuka K; Yoshida T; Kawabata T; Imai A; Mori H; Kimura H; Inada T; Okahisa Y; Egawa J; Usami M; Kushima I; Morikawa M; Okada T; Ikeda M; Branko A; Mori D; Someya T; Iwata N; Ozaki N
    J Neurodev Disord; 2020 Sep; 12(1):25. PubMed ID: 32942984
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
    Cameli C; Viggiano M; Rochat MJ; Maresca A; Caporali L; Fiorini C; Palombo F; Magini P; Duardo RC; Ceroni F; Scaduto MC; Posar A; Seri M; Carelli V; Visconti P; Bacchelli E; Maestrini E
    J Cell Mol Med; 2021 Mar; 25(5):2459-2470. PubMed ID: 33476483
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NRXN1 depletion in the medial prefrontal cortex induces anxiety-like behaviors and abnormal social phenotypes along with impaired neurite outgrowth in rat.
    Wu D; Zhu J; You L; Wang J; Zhang S; Liu Z; Xu Q; Yuan X; Yang L; Wang W; Tong M; Hong Q; Chi X
    J Neurodev Disord; 2023 Feb; 15(1):6. PubMed ID: 36737720
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice.
    Xu B; Ho Y; Fasolino M; Medina J; O'Brien WT; Lamonica JM; Nugent E; Brodkin ES; Fuccillo MV; Bucan M; Zhou Z
    PLoS Genet; 2023 Feb; 19(2):e1010659. PubMed ID: 36848371
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
    Hu Z; Xiao X; Zhang Z; Li M
    Mol Psychiatry; 2019 Oct; 24(10):1400-1414. PubMed ID: 31138894
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings.
    Aksu Uzunhan T; Ayaz A
    Clin Neurol Neurosurg; 2022 Mar; 214():107141. PubMed ID: 35101781
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
    Zweier C; de Jong EK; Zweier M; Orrico A; Ousager LB; Collins AL; Bijlsma EK; Oortveld MA; Ekici AB; Reis A; Schenck A; Rauch A
    Am J Hum Genet; 2009 Nov; 85(5):655-66. PubMed ID: 19896112
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality.
    Lam M; Moslem M; Bryois J; Pronk RJ; Uhlin E; Ellström ID; Laan L; Olive J; Morse R; Rönnholm H; Louhivuori L; Korol SV; Dahl N; Uhlén P; Anderlid BM; Kele M; Sullivan PF; Falk A
    Exp Cell Res; 2019 Oct; 383(1):111469. PubMed ID: 31302032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm gene.
    Hoang N; Yuen RKC; Howe J; Drmic I; Ambrozewicz P; Russell C; Vorstman J; Weiss SK; Anagnostou E; Malow BA; Scherer SW
    Am J Med Genet A; 2021 Apr; 185(4):1120-1130. PubMed ID: 33474825
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure.
    Rhoades R; Henry B; Prichett D; Fang Y; Teng S
    Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627176
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder.
    Yangngam S; Plong-On O; Sripo T; Roongpraiwan R; Hansakunachai T; Wirojanan J; Sombuntham T; Ruangdaraganon N; Limprasert P
    Genet Test Mol Biomarkers; 2014 Jul; 18(7):510-5. PubMed ID: 24832020
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
    Castronovo P; Baccarin M; Ricciardello A; Picinelli C; Tomaiuolo P; Cucinotta F; Frittoli M; Lintas C; Sacco R; Persico AM
    Clin Genet; 2020 Jan; 97(1):125-137. PubMed ID: 30873608
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
    Marcogliese PC; Deal SL; Andrews J; Harnish JM; Bhavana VH; Graves HK; Jangam S; Luo X; Liu N; Bei D; Chao YH; Hull B; Lee PT; Pan H; Bhadane P; Huang MC; Longley CM; Chao HT; Chung HL; Haelterman NA; Kanca O; Manivannan SN; Rossetti LZ; German RJ; Gerard A; Schwaibold EMC; Fehr S; Guerrini R; Vetro A; England E; Murali CN; Barakat TS; van Dooren MF; Wilke M; van Slegtenhorst M; Lesca G; Sabatier I; Chatron N; Brownstein CA; Madden JA; Agrawal PB; Keren B; Courtin T; Perrin L; Brugger M; Roser T; Leiz S; Mau-Them FT; Delanne J; Sukarova-Angelovska E; Trajkova S; Rosenhahn E; Strehlow V; Platzer K; Keller R; Pavinato L; Brusco A; Rosenfeld JA; Marom R; Wangler MF; Yamamoto S
    Cell Rep; 2022 Mar; 38(11):110517. PubMed ID: 35294868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The influence of NRXN1 on systemizing and the brain structure in healthy adults.
    Shiota Y; Matsudaira I; Takeuchi H; Ono C; Tomita H; Kawashima R; Taki Y
    Brain Imaging Behav; 2022 Apr; 16(2):692-701. PubMed ID: 34529206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. NRXN1α
    Avazzadeh S; Quinlan LR; Reilly J; McDonagh K; Jalali A; Wang Y; McInerney V; Krawczyk J; Ding Y; Fitzgerald J; O'Sullivan M; Forman EB; Lynch SA; Ennis S; Feerick N; Reilly R; Li W; Shen X; Yang G; Lu Y; Peeters H; Dockery P; O'Brien T; Shen S; Gallagher L
    BMC Neurosci; 2021 Sep; 22(1):56. PubMed ID: 34525970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disruption of neurexin 1 associated with autism spectrum disorder.
    Kim HG; Kishikawa S; Higgins AW; Seong IS; Donovan DJ; Shen Y; Lally E; Weiss LA; Najm J; Kutsche K; Descartes M; Holt L; Braddock S; Troxell R; Kaplan L; Volkmar F; Klin A; Tsatsanis K; Harris DJ; Noens I; Pauls DL; Daly MJ; MacDonald ME; Morton CC; Quade BJ; Gusella JF
    Am J Hum Genet; 2008 Jan; 82(1):199-207. PubMed ID: 18179900
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.
    Zhao W; Tan J; Zhu T; Ou J; Li Y; Shen L; Wu H; Han L; Liu Y; Jia X; Bai T; Li H; Ke X; Zhao J; Zou X; Hu Z; Guo H; Xia K
    J Genet Genomics; 2019 May; 46(5):247-257. PubMed ID: 31196716
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of the
    Onay H; Kacamak D; Kavasoglu AN; Akgun B; Yalcinli M; Kose S; Ozbaran B
    Balkan J Med Genet; 2016 Dec; 19(2):17-22. PubMed ID: 28289584
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unraveling Mechanisms of Patient-Specific NRXN1 Mutations in Neuropsychiatric Diseases Using Human Induced Pluripotent Stem Cells.
    De Los Angeles A; Tunbridge EM
    Stem Cells Dev; 2020 Sep; 29(17):1142-1144. PubMed ID: 32122280
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.