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 *

140 related articles for article (PubMed ID: 26215504)

  • 21. Effect of 5-HT1A-receptor functional polymorphism on Theory of Mind performances in schizophrenia.
    Bosia M; Anselmetti S; Bechi M; Lorenzi C; Pirovano A; Cocchi F; Buonocore M; Bramanti P; Smeraldi E; Cavallaro R
    Psychiatry Res; 2011 Jul; 188(2):187-90. PubMed ID: 21194755
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.
    Xing J; Wang C; Kimura H; Takasaki Y; Kunimoto S; Yoshimi A; Nakamura Y; Koide T; Banno M; Kushima I; Uno Y; Okada T; Aleksic B; Ikeda M; Iwata N; Ozaki N
    PLoS One; 2014; 9(11):e112531. PubMed ID: 25393624
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Conflict-related anterior cingulate functional connectivity is associated with past suicidal ideation and behavior in recent-onset schizophrenia.
    Minzenberg MJ; Lesh T; Niendam T; Yoon JH; Cheng Y; Rhoades R; Carter CS
    J Psychiatr Res; 2015 Jun; 65():95-101. PubMed ID: 25891474
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel Kidins220/ARMS Splice Isoforms: Potential Specific Regulators of Neuronal and Cardiovascular Development.
    Schmieg N; Thomas C; Yabe A; Lynch DS; Iglesias T; Chakravarty P; Schiavo G
    PLoS One; 2015; 10(6):e0129944. PubMed ID: 26083449
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.
    Suárez-Rama JJ; Arrojo M; Sobrino B; Amigo J; Brenlla J; Agra S; Paz E; Brión M; Carracedo Á; Páramo M; Costas J
    J Psychiatr Res; 2015; 66-67():38-44. PubMed ID: 25943950
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Characterizing genetic variation of adrenergic signalling pathways in Takotsubo (stress) cardiomyopathy exomes.
    Goodloe AH; Evans JM; Middha S; Prasad A; Olson TM
    Eur J Heart Fail; 2014 Sep; 16(9):942-9. PubMed ID: 25132214
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of familial risk for schizophrenia with thalamic and medial prefrontal functional connectivity during attentional control.
    Antonucci LA; Taurisano P; Fazio L; Gelao B; Romano R; Quarto T; Porcelli A; Mancini M; Di Giorgio A; Caforio G; Pergola G; Popolizio T; Bertolino A; Blasi G
    Schizophr Res; 2016 May; 173(1-2):23-9. PubMed ID: 27012899
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neurotrophin and neurotrophin receptor expression by cells of the human lamina cribrosa.
    Lambert W; Agarwal R; Howe W; Clark AF; Wordinger RJ
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2315-23. PubMed ID: 11527945
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neurotrophin signalling in health and disease.
    Chao MV; Rajagopal R; Lee FS
    Clin Sci (Lond); 2006 Feb; 110(2):167-73. PubMed ID: 16411893
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effects of a neuregulin 1 variant on conversion to schizophrenia and schizophreniform disorder in people at high risk for psychosis.
    Kéri S; Kiss I; Kelemen O
    Mol Psychiatry; 2009 Feb; 14(2):118-9. PubMed ID: 19156152
    [No Abstract]   [Full Text] [Related]  

  • 31. HTTLPR functional polymorphism in schizophrenia: executive functions vs. sustained attention dissociation.
    Bosia M; Anselmetti S; Pirovano A; Ermoli E; Marino E; Bramanti P; Smeraldi E; Cavallaro R
    Prog Neuropsychopharmacol Biol Psychiatry; 2010 Feb; 34(1):81-5. PubMed ID: 19818823
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Multiple Rare Risk Coding Variants in Postsynaptic Density-Related Genes Associated With Schizophrenia Susceptibility.
    Hu TM; Wang YC; Wu CL; Hsu SH; Tsai HY; Cheng MC
    Front Genet; 2020; 11():524258. PubMed ID: 33343614
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human and rat hepatic stellate cells express neurotrophins and neurotrophin receptors.
    Cassiman D; Denef C; Desmet VJ; Roskams T
    Hepatology; 2001 Jan; 33(1):148-58. PubMed ID: 11124831
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.
    Griswold AJ; Dueker ND; Van Booven D; Rantus JA; Jaworski JM; Slifer SH; Schmidt MA; Hulme W; Konidari I; Whitehead PL; Cuccaro ML; Martin ER; Haines JL; Gilbert JR; Hussman JP; Pericak-Vance MA
    Mol Autism; 2015; 6():43. PubMed ID: 26185613
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prevention of apoptotic but not necrotic cell death following neuronal injury by neurotrophins signaling through the tyrosine kinase receptor.
    Kim DH; Zhao X; Tu CH; Casaccia-Bonnefil P; Chao MV
    J Neurosurg; 2004 Jan; 100(1):79-87. PubMed ID: 14743916
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia.
    Chang X; Lima LA; Liu Y; Li J; Li Q; Sleiman PMA; Hakonarson H
    Front Genet; 2018; 9():434. PubMed ID: 30323833
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Neurotrophin-3 levels in the cerebrospinal fluid of patients with schizophrenia or medical illness.
    Gilmore JH; Jarskog LF; Lindgren JC; McEvoy JP; Xiao H
    Psychiatry Res; 1997 Nov; 73(1-2):109-13. PubMed ID: 9463844
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prefrontal neuronal integrity predicts symptoms and cognition in schizophrenia and is sensitive to genetic heterogeneity.
    Malaspina D; Kranz TM; Heguy A; Harroch S; Mazgaj R; Rothman K; Berns A; Hasan S; Antonius D; Goetz R; Lazar M; Chao MV; Gonen O
    Schizophr Res; 2016 Apr; 172(1-3):94-100. PubMed ID: 26925801
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa.
    Guo H; Li J; Gao F; Li J; Wu X; Liu Q
    BMC Ophthalmol; 2015 Jul; 15():85. PubMed ID: 26216097
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in human IFT140 cause non-syndromic retinal degeneration.
    Xu M; Yang L; Wang F; Li H; Wang X; Wang W; Ge Z; Wang K; Zhao L; Li H; Li Y; Sui R; Chen R
    Hum Genet; 2015 Oct; 134(10):1069-78. PubMed ID: 26216056
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.