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 *

107 related articles for article (PubMed ID: 36162527)

  • 41. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot.
    Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B
    Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.
    Shi X; Zhang L; Bai K; Xie H; Shi T; Zhang R; Fu Q; Chen S; Lu Y; Yu Y; Sun K
    Comput Struct Biotechnol J; 2020; 18():381-392. PubMed ID: 32128068
    [TBL] [Abstract][Full Text] [Related]  

  • 43. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
    El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S
    Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing.
    Tada H; Hosomichi K; Okada H; Kawashiri MA; Nohara A; Inazu A; Tomizawa S; Tajima A; Mabuchi H; Hayashi K
    Clin Chim Acta; 2016 Jan; 453():194-6. PubMed ID: 26721317
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Tetralogy of fallot as a model to study cardiac progenitor cell migration and differentiation during heart development.
    Di Felice V; Zummo G
    Trends Cardiovasc Med; 2009 May; 19(4):130-5. PubMed ID: 19818949
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Not all pathogenic mutations are pathogenic: KCNH2 mutations in two sisters with tetralogy of Fallot.
    Bhuiyan ZA; Alswaid A; Belfiore M; Al-Ghamdi SS; Liang J; Schlaepffer J
    Int J Cardiol; 2014 Mar; 172(1):276-7. PubMed ID: 24462143
    [No Abstract]   [Full Text] [Related]  

  • 47. Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation.
    Grunert M; Appelt S; Schönhals S; Mika K; Cui H; Cooper A; Cyganek L; Guan K; Sperling SR
    Sci Rep; 2020 Jul; 10(1):10921. PubMed ID: 32616843
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.
    Alharazy S; Naseer MI; Alissa E; Robertson MD; Lanham-New S; Chaudhary AG
    Front Genet; 2021; 12():677780. PubMed ID: 34168679
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
    Qian Y; Xiao D; Guo X; Chen H; Hao L; Ma X; Huang G; Ma D; Wang H
    J Transl Med; 2017 Apr; 15(1):69. PubMed ID: 28372585
    [TBL] [Abstract][Full Text] [Related]  

  • 50. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
    Dasouki MJ; Wakil SM; Al-Harazi O; Alkorashy M; Muiya NP; Andres E; Hagos S; Aldusery H; Dzimiri N; Colak D
    OMICS; 2020 Jan; 24(1):16-28. PubMed ID: 31855513
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mutational and functional analysis of the BVES gene coding region in Chinese patients with non-syndromic tetralogy of Fallot.
    Wu M; Li Y; He X; Shao X; Yang F; Zhao M; Wu C; Zhang C; Zhou L
    Int J Mol Med; 2013 Apr; 31(4):899-903. PubMed ID: 23403794
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot.
    Liu L; Wang HD; Cui CY; Qin YY; Fan TB; Peng BT; Zhang LZ; Wang CZ
    Oncotarget; 2017 Dec; 8(63):106976-106988. PubMed ID: 29291004
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
    Zhao Y; Kang X; Gao F; Guzman A; Lau RP; Biniwale R; Wadehra M; Reemtsen B; Garg M; Halnon N; Quintero-Rivera F; Van Arsdell G; Coppola G; Nelson SF; Touma M;
    J Mol Med (Berl); 2019 Dec; 97(12):1711-1722. PubMed ID: 31834445
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Functionally significant, rare transcription factor variants in tetralogy of Fallot.
    Töpf A; Griffin HR; Glen E; Soemedi R; Brown DL; Hall D; Rahman TJ; Eloranta JJ; Jüngst C; Stuart AG; O'Sullivan J; Keavney BD; Goodship JA
    PLoS One; 2014; 9(8):e95453. PubMed ID: 25093829
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis.
    Peng R; Zheng J; Xie HN; He M; Lin MF
    Cardiovasc Ultrasound; 2019 May; 17(1):8. PubMed ID: 31060568
    [TBL] [Abstract][Full Text] [Related]  

  • 56. First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report.
    Kamal NM; Alzeky AM; Omair MR; Attar RA; Alotaibi AM; Safar A; Alosaimi NS; Abosabie SAS
    Ital J Pediatr; 2022 Jun; 48(1):107. PubMed ID: 35739559
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome.
    Ponikowska M; Pollak A; Kotwica-Strzalek E; Brodowska-Kania D; Mosakowska M; Ploski R; Niemczyk S
    BMC Med Genet; 2020 Oct; 21(1):195. PubMed ID: 33008311
    [TBL] [Abstract][Full Text] [Related]  

  • 58. De novo start-loss variant in HIRA in patient with DiGeorge-like syndrome.
    Maslennikov D; Tolmacheva E; Shubina J; Vasiliev G; Rogacheva M; Svirepova K; Trofimov D
    Clin Genet; 2024 Jun; 105(6):683-685. PubMed ID: 38511226
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Loss of function in
    Kruszka P; Tanpaiboon P; Neas K; Crosby K; Berger SI; Martinez AF; Addissie YA; Pongprot Y; Sittiwangkul R; Silvilairat S; Makonkawkeyoon K; Yu L; Wynn J; Bennett JT; Mefford HC; Reynolds WT; Liu X; Mommersteeg MTM; Chung WK; Lo CW; Muenke M
    J Med Genet; 2017 Dec; 54(12):825-829. PubMed ID: 28592524
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Rare mutations of
    Xie Y; Ma A; Wang B; Peng R; Jing Y; Wang D; Finnell RH; Qiao B; Wang Y; Wang H; Zheng Y
    Clin Sci (Lond); 2019 Jan; 133(2):225-238. PubMed ID: 30610007
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.