BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 26310507)

  • 21. Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy.
    Liu JS; Fan LL; Li JJ; Xiang R
    Am J Cardiol; 2017 May; 119(9):1485-1489. PubMed ID: 28256248
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
    Fressart V; Duthoit G; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Dubourg O; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller D; Hidden-Lucet F; Simon F; Bessirard V; Roux-Buisson N; Hebert JL; Azarine A; Casset-Senon D; Rouzet F; Lecarpentier Y; Fontaine G; Coirault C; Frank R; Hainque B; Charron P
    Europace; 2010 Jun; 12(6):861-8. PubMed ID: 20400443
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Dalal D; James C; Devanagondi R; Tichnell C; Tucker A; Prakasa K; Spevak PJ; Bluemke DA; Abraham T; Russell SD; Calkins H; Judge DP
    J Am Coll Cardiol; 2006 Oct; 48(7):1416-24. PubMed ID: 17010805
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy.
    Protonotarios N; Tsatsopoulou A
    Cardiovasc Pathol; 2004; 13(4):185-94. PubMed ID: 15210133
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation.
    van der Smagt JJ; van der Zwaag PA; van Tintelen JP; Cox MG; Wilde AA; van Langen IM; Ummels A; Hennekam FA; Dooijes D; Gerbens F; Bikker H; Hauer RN; Doevendans PA
    Cardiology; 2012; 123(3):181-9. PubMed ID: 23147395
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Deciphering DSC2 arrhythmogenic cardiomyopathy electrical instability: From ion channels to ECG and tailored drug therapy.
    Moreau A; Reisqs JB; Delanoe-Ayari H; Pierre M; Janin A; Deliniere A; Bessière F; Meli AC; Charrabi A; Lafont E; Valla C; Bauer D; Morel E; Gache V; Millat G; Nissan X; Faucherre A; Jopling C; Richard S; Mejat A; Chevalier P
    Clin Transl Med; 2021 Mar; 11(3):e319. PubMed ID: 33784018
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype.
    López-Ayala JM; Gómez-Milanés I; Sánchez Muñoz JJ; Ruiz-Espejo F; Ortíz M; González-Carrillo J; López-Cuenca D; Oliva-Sandoval MJ; Monserrat L; Valdés M; Gimeno JR
    Europace; 2014 Dec; 16(12):1838-46. PubMed ID: 24938629
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.
    Antoniades L; Tsatsopoulou A; Anastasakis A; Syrris P; Asimaki A; Panagiotakos D; Zambartas C; Stefanadis C; McKenna WJ; Protonotarios N
    Eur Heart J; 2006 Sep; 27(18):2208-16. PubMed ID: 16893920
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features.
    Ghidoni A; Elliott PM; Syrris P; Calkins H; James CA; Judge DP; Murray B; Barc J; Probst V; Schott JJ; Song JP; Hauer RNW; Hoorntje ET; van Tintelen JP; Schulze-Bahr E; Hamilton RM; Mittal K; Semsarian C; Behr ER; Ackerman MJ; Basso C; Parati G; Gentilini D; Kotta MC; Mayosi BM; Schwartz PJ; Crotti L
    Circ Genom Precis Med; 2021 Apr; 14(2):e003097. PubMed ID: 33566628
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical profile in arrhythmogenic cardiomyopathy and a recessive plakophilin-2 gene mutation.
    Ali M; Bhat IA; Hafeez I; Dar MI; Beig JR; Shah ZA; Iqbal K
    Indian Heart J; 2018; 70(3):421-426. PubMed ID: 29961461
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.
    Syrris P; Ward D; Asimaki A; Evans A; Sen-Chowdhry S; Hughes SE; McKenna WJ
    Eur Heart J; 2007 Mar; 28(5):581-8. PubMed ID: 17105751
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Functional Promoter Variant in Desmocollin-2 Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy.
    Christensen AH; Schmitz B; Andersen CB; Bundgaard H; Brand SM; Svendsen JH
    Circ Cardiovasc Genet; 2016 Aug; 9(4):384-7. PubMed ID: 27531918
    [No Abstract]   [Full Text] [Related]  

  • 33. Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy.
    Christensen AH; Benn M; Bundgaard H; Tybjaerg-Hansen A; Haunso S; Svendsen JH
    J Med Genet; 2010 Nov; 47(11):736-44. PubMed ID: 20864495
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.
    Milting H; Klauke B; Christensen AH; Müsebeck J; Walhorn V; Grannemann S; Münnich T; Šarić T; Rasmussen TB; Jensen HK; Mogensen J; Baecker C; Romaker E; Laser KT; zu Knyphausen E; Kassner A; Gummert J; Judge DP; Connors S; Hodgkinson K; Young TL; van der Zwaag PA; van Tintelen JP; Anselmetti D
    Eur Heart J; 2015 Apr; 36(14):872-81. PubMed ID: 24598986
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair.
    Alcalai R; Metzger S; Rosenheck S; Meiner V; Chajek-Shaul T
    J Am Coll Cardiol; 2003 Jul; 42(2):319-27. PubMed ID: 12875771
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
    Brodehl A; Meshkov A; Myasnikov R; Kiseleva A; Kulikova O; Klauke B; Sotnikova E; Stanasiuk C; Divashuk M; Pohl GM; Kudryavtseva M; Klingel K; Gerull B; Zharikova A; Gummert J; Koretskiy S; Schubert S; Mershina E; Gärtner A; Pilus P; Laser KT; Sinitsyn V; Boytsov S; Drapkina O; Milting H
    Int J Mol Sci; 2021 Apr; 22(7):. PubMed ID: 33917638
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two Novel Homozygous Desmoplakin Mutations in Carvajal Syndrome.
    Molho-Pessach V; Sheffer S; Siam R; Tams S; Siam I; Awwad R; Babay S; Golender J; Simanovsky N; Ramot Y; Zlotogorski A
    Pediatr Dermatol; 2015; 32(5):641-6. PubMed ID: 25824144
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial evaluation for diagnosis of arrhythmogenic right ventricular dysplasia.
    Palmisano BT; Rottman JN; Wells QS; DiSalvo TG; Hong CC
    Cardiology; 2011; 119(1):47-53. PubMed ID: 21822014
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).
    McKoy G; Protonotarios N; Crosby A; Tsatsopoulou A; Anastasakis A; Coonar A; Norman M; Baboonian C; Jeffery S; McKenna WJ
    Lancet; 2000 Jun; 355(9221):2119-24. PubMed ID: 10902626
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.
    Aneq MÅ; Fluur C; Rehnberg M; Söderkvist P; Engvall J; Nylander E; Gunnarsson C
    Scand Cardiovasc J; 2012 Apr; 46(2):72-5. PubMed ID: 22035158
    [TBL] [Abstract][Full Text] [Related]  

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