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 *

169 related articles for article (PubMed ID: 31354784)

  • 81. Autism Spectrum Disorder- and/or Intellectual Disability-Associated Semaphorin-5A Exploits the Mechanism by Which Dock5 Signalosome Molecules Control Cell Shape.
    Okabe M; Sato T; Takahashi M; Honjo A; Okawa M; Ishida M; Kukimoto-Niino M; Shirouzu M; Miyamoto Y; Yamauchi J
    Curr Issues Mol Biol; 2024 Apr; 46(4):3092-3107. PubMed ID: 38666924
    [TBL] [Abstract][Full Text] [Related]  

  • 82. RhoG-Binding Domain of Elmo1 Ameliorates Excessive Process Elongation Induced by Autism Spectrum Disorder-Associated Sema5A.
    Okabe M; Miyamoto Y; Ikoma Y; Takahashi M; Shirai R; Kukimoto-Niino M; Shirouzu M; Yamauchi J
    Pathophysiology; 2023 Nov; 30(4):548-566. PubMed ID: 38133141
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Modeling epileptic spasms during infancy: Are we heading for the treatment yet?
    Velíšek L; Velíšková J
    Pharmacol Ther; 2020 Aug; 212():107578. PubMed ID: 32417271
    [TBL] [Abstract][Full Text] [Related]  

  • 84. WDR45 mutations in three male patients with West syndrome.
    Nakashima M; Takano K; Tsuyusaki Y; Yoshitomi S; Shimono M; Aoki Y; Kato M; Aida N; Mizuguchi T; Miyatake S; Miyake N; Osaka H; Saitsu H; Matsumoto N
    J Hum Genet; 2016 Jul; 61(7):653-61. PubMed ID: 27030146
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Infantile spasms syndrome, West syndrome and related phenotypes: what we know in 2013.
    Pavone P; Striano P; Falsaperla R; Pavone L; Ruggieri M
    Brain Dev; 2014 Oct; 36(9):739-51. PubMed ID: 24268986
    [TBL] [Abstract][Full Text] [Related]  

  • 86.
    Wang Q; Liu Z; Lin Z; Zhang R; Lu Y; Su W; Li F; Xu X; Tu M; Lou Y; Zhao J; Zheng X
    Front Genet; 2019; 10():605. PubMed ID: 31354784
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.
    Liu Z; Li Z; Zhi X; Du Y; Lin Z; Wu J
    Mol Neurobiol; 2018 Mar; 55(3):2483-2493. PubMed ID: 28386848
    [TBL] [Abstract][Full Text] [Related]  

  • 88. A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.
    Mosca-Boidron AL; Gueneau L; Huguet G; Goldenberg A; Henry C; Gigot N; Pallesi-Pocachard E; Falace A; Duplomb L; Thevenon J; Duffourd Y; St-Onge J; Chambon P; Rivière JB; Thauvin-Robinet C; Callier P; Marle N; Payet M; Ragon C; Goubran Botros H; Buratti J; Calderari S; Dumas G; Delorme R; Lagarde N; Pinoit JM; Rosier A; Masurel-Paulet A; Cardoso C; Mugneret F; Saugier-Veber P; Campion D; Faivre L; Bourgeron T
    Eur J Hum Genet; 2016 Jun; 24(6):838-43. PubMed ID: 26395558
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies.
    Lin Z; Liu Z; Li X; Li F; Hu Y; Chen B; Wang Z; Liu Y
    Sci Rep; 2017 Mar; 7(1):258. PubMed ID: 28325891
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
    Gerald B; Ramsey K; Belnap N; Szelinger S; Siniard AL; Balak C; Russell M; Richholt R; De Both M; Claasen AM; Schrauwen I; Huentelman MJ; Craig DW; Rangasamy S; Narayanan V
    Semin Pediatr Neurol; 2018 Jul; 26():28-32. PubMed ID: 29961512
    [TBL] [Abstract][Full Text] [Related]  

  • 91.
    Zhang X; Xiao N; Cao Y; Peng Y; Lian A; Chen Y; Wang P; Gu W; Xiao B; Yu J; Wang H; Shu L
    Front Mol Neurosci; 2023; 16():1097553. PubMed ID: 36910266
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies.
    He N; Lin ZJ; Wang J; Wei F; Meng H; Liu XR; Chen Q; Su T; Shi YW; Yi YH; Liao WP
    Genet Med; 2019 Jan; 21(1):17-27. PubMed ID: 29895856
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Clathrin heavy chain 22 contributes to the control of neuropeptide degradation and secretion during neuronal development.
    Nahorski MS; Borner GHH; Shaikh SS; Davies AK; Al-Gazali L; Antrobus R; Woods CG
    Sci Rep; 2018 Feb; 8(1):2340. PubMed ID: 29402896
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
    Jin ZB; Li Z; Liu Z; Jiang Y; Cai XB; Wu J
    Biol Rev Camb Philos Soc; 2018 May; 93(2):1014-1031. PubMed ID: 29154454
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Autism spectrum disorder and epileptic encephalopathy: common causes, many questions.
    Srivastava S; Sahin M
    J Neurodev Disord; 2017; 9():23. PubMed ID: 28649286
    [TBL] [Abstract][Full Text] [Related]  

  • 96. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
    Scheffer IE; Berkovic S; Capovilla G; Connolly MB; French J; Guilhoto L; Hirsch E; Jain S; Mathern GW; Moshé SL; Nordli DR; Perucca E; Tomson T; Wiebe S; Zhang YH; Zuberi SM
    Epilepsia; 2017 Apr; 58(4):512-521. PubMed ID: 28276062
    [TBL] [Abstract][Full Text] [Related]  

  • 97.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 98.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 99.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 100.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.