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 *

165 related articles for article (PubMed ID: 33959666)

  • 1. Whole-Exome Sequencing Identifies a Novel
    Dong Y; Du R; Fan LL; Jin JY; Huang H; Chen YQ; Bi DD; Xiang R
    Biomed Res Int; 2021; 2021():9247541. PubMed ID: 33959666
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Role of
    Palladino A; Papa AA; Petillo R; Scutifero M; Morra S; Passamano L; Nigro V; Politano L
    Genes (Basel); 2022 Jan; 13(2):. PubMed ID: 35205305
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.
    Syam N; Chatel S; Ozhathil LC; Sottas V; Rougier JS; Baruteau A; Baron E; Amarouch MY; Daumy X; Probst V; Schott JJ; Abriel H
    J Am Heart Assoc; 2016 May; 5(5):. PubMed ID: 27207958
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel missense variant in TTN cosegregating with familial atrioventricular block.
    Liu G; Yang Z; Chen W; Xu J; Mao L; Yu Q; Guo J; Xu H; Liu F; Sun Y; Huang H; Peng Z; Sun J; Li W; Yang P
    Eur J Med Genet; 2020 Mar; 63(3):103752. PubMed ID: 31470098
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbances.
    Stallmeyer B; Zumhagen S; Denjoy I; Duthoit G; Hébert JL; Ferrer X; Maugenre S; Schmitz W; Kirchhefer U; Schulze-Bahr E; Guicheney P; Schulze-Bahr E
    Hum Mutat; 2012 Jan; 33(1):109-17. PubMed ID: 21887725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transient receptor potential melastatin 4 cation channel in pediatric heart block.
    Tian J; An XJ; Fu MY
    Eur Rev Med Pharmacol Sci; 2017 Oct; 21(4 Suppl):79-84. PubMed ID: 29165759
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Mutation in the G-Protein Gene
    Stallmeyer B; Kuß J; Kotthoff S; Zumhagen S; Vowinkel K; Rinné S; Matschke LA; Friedrich C; Schulze-Bahr E; Rust S; Seebohm G; Decher N; Schulze-Bahr E
    Circ Res; 2017 May; 120(10):e33-e44. PubMed ID: 28219978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.
    Kruse M; Schulze-Bahr E; Corfield V; Beckmann A; Stallmeyer B; Kurtbay G; Ohmert I; Schulze-Bahr E; Brink P; Pongs O
    J Clin Invest; 2009 Sep; 119(9):2737-44. PubMed ID: 19726882
    [TBL] [Abstract][Full Text] [Related]  

  • 9. POPDC2 a novel susceptibility gene for conduction disorders.
    Rinné S; Ortiz-Bonnin B; Stallmeyer B; Kiper AK; Fortmüller L; Schindler RFR; Herbort-Brand U; Kabir NS; Dittmann S; Friedrich C; Zumhagen S; Gualandi F; Selvatici R; Rapezzi C; Arbustini E; Ferlini A; Fabritz L; Schulze-Bahr E; Brand T; Decher N
    J Mol Cell Cardiol; 2020 Aug; 145():74-83. PubMed ID: 32535041
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TRPM4 channels in the cardiovascular system.
    Kruse M; Pongs O
    Curr Opin Pharmacol; 2014 Apr; 15():68-73. PubMed ID: 24721656
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.
    Daumy X; Amarouch MY; Lindenbaum P; Bonnaud S; Charpentier E; Bianchi B; Nafzger S; Baron E; Fouchard S; Thollet A; Kyndt F; Barc J; Le Scouarnec S; Makita N; Le Marec H; Dina C; Gourraud JB; Probst V; Abriel H; Redon R; Schott JJ
    Int J Cardiol; 2016 Mar; 207():349-58. PubMed ID: 26820365
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of genetic testing in young patients with idiopathic atrioventricular conduction disease.
    Auricchio A; Demarchi A; Özkartal T; Campanale D; Caputo ML; di Valentino M; Menafoglio A; Regoli F; Facchini M; Del Bufalo A; Foglia P; Ferrari N; Bomio F; Medeiros-Domingo A; Moccetti T; Pedrazzini GB; Klersy C; Conte G
    Europace; 2023 Feb; 25(2):643-650. PubMed ID: 36352534
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia.
    Wang H; Xu Z; Lee BH; Vu S; Hu L; Lee M; Bu D; Cao X; Hwang S; Yang Y; Zheng J; Lin Z
    J Invest Dermatol; 2019 May; 139(5):1089-1097. PubMed ID: 30528822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.
    Xu YJ; Qiu XB; Yuan F; Shi HY; Xu L; Hou XM; Qu XK; Liu X; Huang RT; Xue S; Yang YQ; Li RG
    Mol Med Rep; 2017 Apr; 15(4):2247-2254. PubMed ID: 28259982
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A G613A missense in the Hutchinson's progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block.
    Villa F; Maciąg A; Spinelli CC; Ferrario A; Carrizzo A; Parisi A; Torella A; Montenero C; Condorelli G; Vecchione C; Nigro V; Montenero AS; Puca AA
    Immun Ageing; 2014; 11(1):19. PubMed ID: 25469153
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional characterization of TRPM4 variants identified in sudden unexpected natural death.
    Subbotina E; Williams N; Sampson BA; Tang Y; Coetzee WA
    Forensic Sci Int; 2018 Dec; 293():37-46. PubMed ID: 30391667
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Implication of the TRPM4 nonselective cation channel in mammalian sinus rhythm.
    Hof T; Simard C; Rouet R; Sallé L; Guinamard R
    Heart Rhythm; 2013 Nov; 10(11):1683-9. PubMed ID: 23954346
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel.
    Liu H; Chatel S; Simard C; Syam N; Salle L; Probst V; Morel J; Millat G; Lopez M; Abriel H; Schott JJ; Guinamard R; Bouvagnet P
    PLoS One; 2013; 8(1):e54131. PubMed ID: 23382873
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Aberrant Deactivation-Induced Gain of Function in TRPM4 Mutant Is Associated with Human Cardiac Conduction Block.
    Xian W; Hui X; Tian Q; Wang H; Moretti A; Laugwitz KL; Flockerzi V; Ruppenthal S; Lipp P
    Cell Rep; 2018 Jul; 24(3):724-731. PubMed ID: 30021168
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia.
    Huang H; Ding DB; Fan LL; Jin JY; Li JJ; Guo S; Chen YQ; Xiang R
    Cardiol Young; 2018 May; 28(5):688-691. PubMed ID: 29402340
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.