BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 34514717)

  • 1. Soma-to-germline transformation in chromatin-linked neurodevelopmental disorders?
    Bonefas KM; Iwase S
    FEBS J; 2022 Apr; 289(8):2301-2317. PubMed ID: 34514717
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reprogramming of the epigenome in neurodevelopmental disorders.
    Wilson KD; Porter EG; Garcia BA
    Crit Rev Biochem Mol Biol; 2022 Feb; 57(1):73-112. PubMed ID: 34601997
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and cellular events linking variants in the histone demethylase KDM5C to the intellectual disability disorder Claes-Jensen syndrome.
    Hatch HAM; Secombe J
    FEBS J; 2022 Dec; 289(24):7776-7787. PubMed ID: 34536985
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies.
    Nixon KCJ; Rousseau J; Stone MH; Sarikahya M; Ehresmann S; Mizuno S; Matsumoto N; Miyake N; ; Baralle D; McKee S; Izumi K; Ritter AL; Heide S; Héron D; Depienne C; Titheradge H; Kramer JM; Campeau PM
    Am J Hum Genet; 2019 Apr; 104(4):596-610. PubMed ID: 30879640
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.
    Küry S; Ebstein F; Mollé A; Besnard T; Lee MK; Vignard V; Hery T; Nizon M; Mancini GMS; Giltay JC; Cogné B; McWalter K; Deb W; Mor-Shaked H; Li H; Schnur RE; Wentzensen IM; Denommé-Pichon AS; Fourgeux C; Verheijen FW; Faurie E; Schot R; Stevens CA; Smits DJ; Barr E; Sheffer R; Bernstein JA; Stimach CL; Kovitch E; Shashi V; Schoch K; Smith W; van Jaarsveld RH; Hurst ACE; Smith K; Baugh EH; Bohm SG; Vyhnálková E; Ryba L; Delnatte C; Neira J; Bonneau D; Toutain A; Rosenfeld JA; ; Audebert-Bellanger S; Gilbert-Dussardier B; Odent S; Laumonnier F; Berger SI; Smith ACM; Bourdeaut F; Stern MH; Redon R; Krüger E; Margueron R; Bézieau S; Poschmann J; Isidor B
    Am J Hum Genet; 2022 Feb; 109(2):361-372. PubMed ID: 35051358
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epigenetic Etiology of Intellectual Disability.
    Iwase S; Bérubé NG; Zhou Z; Kasri NN; Battaglioli E; Scandaglia M; Barco A
    J Neurosci; 2017 Nov; 37(45):10773-10782. PubMed ID: 29118205
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Expanding the Spectrum of
    Lintas C; Bottillo I; Sacco R; Azzarà A; Cassano I; Ciccone MP; Grammatico P; Gurrieri F
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553533
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.
    Poeta L; Padula A; Lioi MB; van Bokhoven H; Miano MG
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356104
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sexually Dimorphic Alterations in the Transcriptome and Behavior with Loss of Histone Demethylase
    Bonefas KM; Vallianatos CN; Raines B; Tronson NC; Iwase S
    Cells; 2023 Feb; 12(4):. PubMed ID: 36831303
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders.
    Prem S; Millonig JH; DiCicco-Bloom E
    Adv Neurobiol; 2020; 25():109-153. PubMed ID: 32578146
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective.
    Mossink B; Negwer M; Schubert D; Nadif Kasri N
    Cell Mol Life Sci; 2021 Mar; 78(6):2517-2563. PubMed ID: 33263776
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
    Gillentine MA; Wang T; Hoekzema K; Rosenfeld J; Liu P; Guo H; Kim CN; De Vries BBA; Vissers LELM; Nordenskjold M; Kvarnung M; Lindstrand A; Nordgren A; Gecz J; Iascone M; Cereda A; Scatigno A; Maitz S; Zanni G; Bertini E; Zweier C; Schuhmann S; Wiesener A; Pepper M; Panjwani H; Torti E; Abid F; Anselm I; Srivastava S; Atwal P; Bacino CA; Bhat G; Cobian K; Bird LM; Friedman J; Wright MS; Callewaert B; Petit F; Mathieu S; Afenjar A; Christensen CK; White KM; Elpeleg O; Berger I; Espineli EJ; Fagerberg C; Brasch-Andersen C; Hansen LK; Feyma T; Hughes S; Thiffault I; Sullivan B; Yan S; Keller K; Keren B; Mignot C; Kooy F; Meuwissen M; Basinger A; Kukolich M; Philips M; Ortega L; Drummond-Borg M; Lauridsen M; Sorensen K; Lehman A; ; Lopez-Rangel E; Levy P; Lessel D; Lotze T; Madan-Khetarpal S; Sebastian J; Vento J; Vats D; Benman LM; Mckee S; Mirzaa GM; Muss C; Pappas J; Peeters H; Romano C; Elia M; Galesi O; Simon MEH; van Gassen KLI; Simpson K; Stratton R; Syed S; Thevenon J; Palafoll IV; Vitobello A; Bournez M; Faivre L; Xia K; ; Earl RK; Nowakowski T; Bernier RA; Eichler EE
    Genome Med; 2021 Apr; 13(1):63. PubMed ID: 33874999
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
    Jin B; Tao Q; Peng J; Soo HM; Wu W; Ying J; Fields CR; Delmas AL; Liu X; Qiu J; Robertson KD
    Hum Mol Genet; 2008 Mar; 17(5):690-709. PubMed ID: 18029387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dendritic Integration Dysfunction in Neurodevelopmental Disorders.
    Nelson AD; Bender KJ
    Dev Neurosci; 2021; 43(3-4):201-221. PubMed ID: 34139699
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability.
    Weil D; Piton A; Lessel D; Standart N
    Biochem Soc Trans; 2020 Jun; 48(3):1199-1211. PubMed ID: 32412080
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development and disease in a dish: the epigenetics of neurodevelopmental disorders.
    Lewis EM; Kroll KL
    Epigenomics; 2018 Feb; 10(2):219-231. PubMed ID: 29334242
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Contribution of spurious transcription to intellectual disability disorders.
    Scandaglia M; Barco A
    J Med Genet; 2019 Aug; 56(8):491-498. PubMed ID: 30745423
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recent advances in gene therapy for neurodevelopmental disorders with epilepsy.
    Turner TJ; Zourray C; Schorge S; Lignani G
    J Neurochem; 2021 Apr; 157(2):229-262. PubMed ID: 32880951
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pathogenic
    Song JM; Kang M; Park DH; Park S; Lee S; Suh YH
    J Neurosci; 2021 Mar; 41(11):2344-2359. PubMed ID: 33500274
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The chromatin basis of neurodevelopmental disorders: Rethinking dysfunction along the molecular and temporal axes.
    Gabriele M; Lopez Tobon A; D'Agostino G; Testa G
    Prog Neuropsychopharmacol Biol Psychiatry; 2018 Jun; 84(Pt B):306-327. PubMed ID: 29309830
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.