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 *

197 related articles for article (PubMed ID: 20194882)

  • 1. Protein aggregates and novel presenilin gene variants in idiopathic dilated cardiomyopathy.
    Gianni D; Li A; Tesco G; McKay KM; Moore J; Raygor K; Rota M; Gwathmey JK; Dec GW; Aretz T; Leri A; Semigran MJ; Anversa P; Macgillivray TE; Tanzi RE; del Monte F
    Circulation; 2010 Mar; 121(10):1216-26. PubMed ID: 20194882
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations of presenilin genes in dilated cardiomyopathy and heart failure.
    Li D; Parks SB; Kushner JD; Nauman D; Burgess D; Ludwigsen S; Partain J; Nixon RR; Allen CN; Irwin RP; Jakobs PM; Litt M; Hershberger RE
    Am J Hum Genet; 2006 Dec; 79(6):1030-9. PubMed ID: 17186461
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel polymorphisms in PDLIM3 and PDLIM5 gene encoding Z-line proteins increase risk of idiopathic dilated cardiomyopathy.
    Wang D; Fang J; Lv J; Pan Z; Yin X; Cheng H; Guo X
    J Cell Mol Med; 2019 Oct; 23(10):7054-7062. PubMed ID: 31424159
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphisms of presenilin-1 gene associate with dilated cardiomyopathy susceptibility.
    Li H; Chen Y; Zhou B; Peng Y; Sheng Y; Rao L
    Mol Cell Biochem; 2011 Dec; 358(1-2):31-6. PubMed ID: 21656036
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.
    Wong TH; Seelaar H; Melhem S; Rozemuller AJM; van Swieten JC
    Neurobiol Aging; 2020 Feb; 86():201.e9-201.e14. PubMed ID: 30797548
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of stability and hydrophobicity of presenilin 1 mutations causing Alzheimer's disease.
    Somavarapu AK; Kepp KP
    J Neurochem; 2016 Apr; 137(1):101-11. PubMed ID: 26756738
    [TBL] [Abstract][Full Text] [Related]  

  • 7. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
    Lanoiselée HM; Nicolas G; Wallon D; Rovelet-Lecrux A; Lacour M; Rousseau S; Richard AC; Pasquier F; Rollin-Sillaire A; Martinaud O; Quillard-Muraine M; de la Sayette V; Boutoleau-Bretonniere C; Etcharry-Bouyx F; Chauviré V; Sarazin M; le Ber I; Epelbaum S; Jonveaux T; Rouaud O; Ceccaldi M; Félician O; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Chamard L; Vincent JL; Sauvée M; Marelli-Tosi C; Gabelle A; Ozsancak C; Pariente J; Paquet C; Hannequin D; Campion D;
    PLoS Med; 2017 Mar; 14(3):e1002270. PubMed ID: 28350801
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial Alzheimer's disease presenilin-2 mutants affect Ca
    Pendin D; Fasolato C; Basso E; Filadi R; Greotti E; Galla L; Gomiero C; Leparulo A; Redolfi N; Scremin E; Vajente N; Pozzan T; Pizzo P
    Aging Clin Exp Res; 2021 Jun; 33(6):1705-1708. PubMed ID: 31606858
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial Alzheimer's Disease Mutations in Presenilin Generate Amyloidogenic Aβ Peptide Seeds.
    Veugelen S; Saito T; Saido TC; Chávez-Gutiérrez L; De Strooper B
    Neuron; 2016 Apr; 90(2):410-6. PubMed ID: 27100199
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PSEN1 and PSEN2 gene expression in Alzheimer's disease brain: a new approach.
    Delabio R; Rasmussen L; Mizumoto I; Viani GA; Chen E; Villares J; Costa IB; Turecki G; Linde SA; Smith MC; Payão SL
    J Alzheimers Dis; 2014; 42(3):757-60. PubMed ID: 24927704
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Discovery and validation of autosomal dominant Alzheimer's disease mutations.
    Hsu S; Gordon BA; Hornbeck R; Norton JB; Levitch D; Louden A; Ziegemeier E; Laforce R; Chhatwal J; Day GS; McDade E; Morris JC; Fagan AM; Benzinger TLS; Goate AM; Cruchaga C; Bateman RJ; ; Karch CM
    Alzheimers Res Ther; 2018 Jul; 10(1):67. PubMed ID: 30021643
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human cardiac-specific cDNA array for idiopathic dilated cardiomyopathy: sex-related differences.
    Haddad GE; Saunders LJ; Crosby SD; Carles M; del Monte F; King K; Bristow MR; Spinale FG; Macgillivray TE; Semigran MJ; Dec GW; Williams SA; Hajjar RJ; Gwathmey JK
    Physiol Genomics; 2008 Apr; 33(2):267-77. PubMed ID: 18303083
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exploring the Role of Aggregated Proteomes in the Pathogenesis of Alzheimer's Disease.
    Narayanan SE; Sekhar N; Rajamma RG; Marathakam A; Al Mamun A; Uddin MS; Mathew B
    Curr Protein Pept Sci; 2020; 21(12):1164-1173. PubMed ID: 32957903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of the regional responsivity to ryanodine of human myocardium from patients with idiopathic dilated cardiomyopathy and secondary cardiomyopathies.
    Padrini R; Panfili M; Testolin L; Pesarin F; Piovan D; Magnolfi G; Livi U; Casarotto D; Dalla Volta S
    Basic Res Cardiol; 1996; 91(5):361-6. PubMed ID: 8922253
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A promoter polymorphism -945C>G in the connective tissue growth factor in heart failure patients with mechanical circulatory support: a new marker for bridge to recovery?
    Posch MG; Schmidt G; Steinhoff L; Perrot A; Drews T; Dandel M; Krabatsch T; Hetzer R; Potapov EV
    Eur J Cardiothorac Surg; 2015 Jan; 47(1):e29-33. PubMed ID: 25349161
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population].
    Chen B; Rao L; Zhou B; Liu X; Hang P; Wu Y; Peng Y; Chen Y
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2008 Nov; 39(6):969-72. PubMed ID: 19253838
    [TBL] [Abstract][Full Text] [Related]  

  • 17. TNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han Chinese.
    Li YD; Ji YT; Zhou XH; Li HL; Zhang HT; Xing Q; Hong YF; Tang BP
    Med Sci Monit; 2015 Nov; 21():3343-7. PubMed ID: 26525169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cofilin-2 phosphorylation and sequestration in myocardial aggregates: novel pathogenetic mechanisms for idiopathic dilated cardiomyopathy.
    Subramanian K; Gianni D; Balla C; Assenza GE; Joshi M; Semigran MJ; Macgillivray TE; Van Eyk JE; Agnetti G; Paolocci N; Bamburg JR; Agrawal PB; Del Monte F
    J Am Coll Cardiol; 2015 Mar; 65(12):1199-1214. PubMed ID: 25814227
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New insights into lipid raft function regulating myocardial vascularization competency in human idiopathic dilated cardiomyopathy.
    Roura S; Gálvez-Montón C; Pujal JM; Casani L; Fernández MA; Astier L; Gastelurrutia P; Domingo M; Prat-Vidal C; Soler-Botija C; Llucià-Valldeperas A; Llorente-Cortés V; Bayes-Genis A
    Atherosclerosis; 2013 Oct; 230(2):354-64. PubMed ID: 24075768
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac adenovirus-associated viral Presenilin 1 gene delivery protects the left ventricular function of the heart via regulating RyR2 function in post-ischaemic heart failure.
    Li T; Shen Y; Su L; Fan X; Lin F; Ye X; Ding D; Tang Y; Yang Y; Lei C; Hu S
    J Drug Target; 2018 Dec; 26(10):895-904. PubMed ID: 29521549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.