BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 29804726)

  • 1. Short Telomere Syndromes in Clinical Practice: Bridging Bench and Bedside.
    Mangaonkar AA; Patnaik MM
    Mayo Clin Proc; 2018 Jul; 93(7):904-916. PubMed ID: 29804726
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Correlates and Treatment Outcomes for Patients With Short Telomere Syndromes.
    Mangaonkar AA; Ferrer A; Pinto E Vairo F; Cousin MA; Kuisle RJ; Klee EW; Kennedy CC; Peters SG; Scott JP; Utz JP; Baqir M; Sekiguchi H; Khan SP; Rodriguez V; Simonetto DA; Kamath PS; Abraham RS; Wylam ME; Patnaik MM
    Mayo Clin Proc; 2018 Jul; 93(7):834-839. PubMed ID: 29976374
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pulmonary Fibrosis and a TERT Founder Mutation With a Latency Period of 300 Years.
    van der Vis JJ; van der Smagt JJ; Hennekam FAM; Grutters JC; van Moorsel CHM
    Chest; 2020 Aug; 158(2):612-619. PubMed ID: 32315675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Short Telomere Syndrome presenting with pulmonary fibrosis, liver cirrhosis and hepatopulmonary syndrome: a case report.
    Baird A; Gomes M; Souza CA; Magner K; Alvarez G
    BMC Pulm Med; 2023 Apr; 23(1):114. PubMed ID: 37041499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Telomerase gene mutations and telomere length shortening in patients with idiopathic pulmonary fibrosis in a Chinese population.
    Dai J; Cai H; Zhuang Y; Wu Y; Min H; Li J; Shi Y; Gao Q; Yi L
    Respirology; 2015 Jan; 20(1):122-8. PubMed ID: 25346280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Successful liver transplantation in short telomere syndromes without bone marrow failure due to DKC1 mutation.
    Del Brío Castillo R; Bleesing J; McCormick T; Squires JE; Mazariegos GV; Squires J; McKiernan PJ
    Pediatr Transplant; 2020 May; 24(3):e13695. PubMed ID: 32166868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cancer spectrum and outcomes in the Mendelian short telomere syndromes.
    Schratz KE; Haley L; Danoff SK; Blackford AL; DeZern AE; Gocke CD; Duffield AS; Armanios M
    Blood; 2020 May; 135(22):1946-1956. PubMed ID: 32076714
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Telomeres and marrow failure.
    Calado RT
    Hematology Am Soc Hematol Educ Program; 2009; ():338-43. PubMed ID: 20008219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Telomere homeostasis in trophoblasts and in cord blood cells from pregnancies complicated with preeclampsia.
    Sukenik-Halevy R; Amiel A; Kidron D; Liberman M; Ganor-Paz Y; Biron-Shental T
    Am J Obstet Gynecol; 2016 Feb; 214(2):283.e1-283.e7. PubMed ID: 26321036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The effect of TERC haploinsufficiency on the inheritance of telomere length.
    Goldman F; Bouarich R; Kulkarni S; Freeman S; Du HY; Harrington L; Mason PJ; Londoño-Vallejo A; Bessler M
    Proc Natl Acad Sci U S A; 2005 Nov; 102(47):17119-24. PubMed ID: 16284252
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations.
    van der Vis JJ; van der Smagt JJ; van Batenburg AA; Goldschmeding R; van Es HW; Grutters JC; van Moorsel CHM
    Respirology; 2021 Dec; 26(12):1160-1170. PubMed ID: 34580961
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reversibility of Defective Hematopoiesis Caused by Telomere Shortening in Telomerase Knockout Mice.
    Raval A; Behbehani GK; Nguyen le XT; Thomas D; Kusler B; Garbuzov A; Ramunas J; Holbrook C; Park CY; Blau H; Nolan GP; Artandi SE; Mitchell BS
    PLoS One; 2015; 10(7):e0131722. PubMed ID: 26133370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Telomere shortening activates TGF-β/Smads signaling in lungs and enhances both lipopolysaccharide and bleomycin-induced pulmonary fibrosis.
    Liu YY; Shi Y; Liu Y; Pan XH; Zhang KX
    Acta Pharmacol Sin; 2018 Nov; 39(11):1735-1745. PubMed ID: 29925920
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.
    Arias-Salgado EG; Galvez E; Planas-Cerezales L; Pintado-Berninches L; Vallespin E; Martinez P; Carrillo J; Iarriccio L; Ruiz-Llobet A; Catalá A; Badell-Serra I; Gonzalez-Granado LI; Martín-Nalda A; Martínez-Gallo M; Galera-Miñarro A; Rodríguez-Vigil C; Bastos-Oreiro M; Perez de Nanclares G; Leiro-Fernández V; Uria ML; Diaz-Heredia C; Valenzuela C; Martín S; López-Muñiz B; Lapunzina P; Sevilla J; Molina-Molina M; Perona R; Sastre L
    Orphanet J Rare Dis; 2019 Apr; 14(1):82. PubMed ID: 30995915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Telomere length abnormalities and telomerase RNA component expression in gastroenteropancreatic neuroendocrine tumors.
    Kim HS; Lee HS; Nam KH; Choi J; Kim WH
    Anticancer Res; 2015 Jun; 35(6):3501-10. PubMed ID: 26026117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
    Alter BP; Baerlocher GM; Savage SA; Chanock SJ; Weksler BB; Willner JP; Peters JA; Giri N; Lansdorp PM
    Blood; 2007 Sep; 110(5):1439-47. PubMed ID: 17468339
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for genetic anticipation in vonHippel-Lindau syndrome.
    Aronoff L; Malkin D; van Engelen K; Gallinger B; Wasserman J; Kim RH; Villani A; Meyn MS; Druker H
    J Med Genet; 2018 Jun; 55(6):395-402. PubMed ID: 29437867
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnostic utility of telomere length testing in a hospital-based setting.
    Alder JK; Hanumanthu VS; Strong MA; DeZern AE; Stanley SE; Takemoto CM; Danilova L; Applegate CD; Bolton SG; Mohr DW; Brodsky RA; Casella JF; Greider CW; Jackson JB; Armanios M
    Proc Natl Acad Sci U S A; 2018 Mar; 115(10):E2358-E2365. PubMed ID: 29463756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Telomere length dynamics in normal individuals and in patients with hematopoietic stem cell-associated disorders.
    Brümmendorf TH; Rufer N; Holyoake TL; Maciejewski J; Barnett MJ; Eaves CJ; Eaves AC; Young N; Lansdorp PM
    Ann N Y Acad Sci; 2001 Jun; 938():293-303; discussion 303-4. PubMed ID: 11458518
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shortening.
    Carrillo J; Calvete O; Pintado-Berninches L; Manguan-García C; Sevilla Navarro J; Arias-Salgado EG; Sastre L; Guenechea G; López Granados E; de Villartay JP; Revy P; Benitez J; Perona R
    Hum Mol Genet; 2017 May; 26(10):1900-1914. PubMed ID: 28369633
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.