187 related articles for article (PubMed ID: 19415813)
1. An atypical form of dyskeratosis congenita with renal agenesis and no mutation in DKC1, TERC and TERT genes.
Balci S; Engiz O; Erekul A; Gozdasoglu S; Vulliamy T
J Eur Acad Dermatol Venereol; 2009 May; 23(5):607-8. PubMed ID: 19415813
[No Abstract] [Full Text] [Related]
2. Dyskeratosis congenita: molecular insights into telomerase function, ageing and cancer.
Marrone A; Dokal I
Expert Rev Mol Med; 2004 Dec; 6(26):1-23. PubMed ID: 15613268
[TBL] [Abstract][Full Text] [Related]
3. Dyskeratosis congenita.
Handley TP; McCaul JA; Ogden GR
Oral Oncol; 2006 Apr; 42(4):331-6. PubMed ID: 16140563
[TBL] [Abstract][Full Text] [Related]
4. Dyskeratosis congenita: a genetic disorder of many faces.
Kirwan M; Dokal I
Clin Genet; 2008 Feb; 73(2):103-12. PubMed ID: 18005359
[TBL] [Abstract][Full Text] [Related]
5. Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantation.
de la Fuente J; Dokal I
Pediatr Transplant; 2007 Sep; 11(6):584-94. PubMed ID: 17663679
[TBL] [Abstract][Full Text] [Related]
6. Telomerase RNA structure and function: implications for dyskeratosis congenita.
Chen JL; Greider CW
Trends Biochem Sci; 2004 Apr; 29(4):183-92. PubMed ID: 15082312
[No Abstract] [Full Text] [Related]
7. Mutations of telomerase complex genes linked to bone marrow failures.
Yamaguchi H
J Nippon Med Sch; 2007 Jun; 74(3):202-9. PubMed ID: 17625368
[TBL] [Abstract][Full Text] [Related]
8. Novel mutations of the DKC1 gene in individuals affected with dyskeratosis congenita.
Rostamiani K; Klauck SM; Heiss N; Poustka A; Khaleghi M; Rosales R; Metzenberg AB
Blood Cells Mol Dis; 2010; 44(2):88. PubMed ID: 19879169
[No Abstract] [Full Text] [Related]
9. Identification of a novel mutation in DKC1 in dyskeratosis congenita.
Kurnikova M; Shagina I; Khachatryan L; Schagina O; Maschan M; Shagin D
Pediatr Blood Cancer; 2009 Jan; 52(1):135-7. PubMed ID: 18802941
[TBL] [Abstract][Full Text] [Related]
10. Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice.
He J; Navarrete S; Jasinski M; Vulliamy T; Dokal I; Bessler M; Mason PJ
Oncogene; 2002 Oct; 21(50):7740-4. PubMed ID: 12400016
[TBL] [Abstract][Full Text] [Related]
11. [Bone marrow failure due to telomere associated gene mutation].
Yamaguchi H; Dan K
Rinsho Ketsueki; 2010 Aug; 51(8):646-53. PubMed ID: 20805671
[No Abstract] [Full Text] [Related]
12. [Bone marrow failure due to telomerase complex gene mutations].
Yamaguchi H
Rinsho Ketsueki; 2006 Nov; 47(11):1431-7. PubMed ID: 17176885
[No Abstract] [Full Text] [Related]
13. Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification.
Ruggero D; Grisendi S; Piazza F; Rego E; Mari F; Rao PH; Cordon-Cardo C; Pandolfi PP
Science; 2003 Jan; 299(5604):259-62. PubMed ID: 12522253
[TBL] [Abstract][Full Text] [Related]
14. A novel missense mutation in the DKC1 gene in a Japanese family with X-linked dyskeratosis congenita.
Hiramatsu H; Fujii T; Kitoh T; Sawada M; Osaka M; Koami K; Irino T; Miyajima T; Ito M; Sugiyama T; Okuno T
Pediatr Hematol Oncol; 2002 Sep; 19(6):413-9. PubMed ID: 12186364
[TBL] [Abstract][Full Text] [Related]
15. Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome.
Yaghmai R; Kimyai-Asadi A; Rostamiani K; Heiss NS; Poustka A; Eyaid W; Bodurtha J; Nousari HC; Hamosh A; Metzenberg A
J Pediatr; 2000 Mar; 136(3):390-3. PubMed ID: 10700698
[TBL] [Abstract][Full Text] [Related]
16. Comparable Effects of the Androgen Derivatives Danazol, Oxymetholone and Nandrolone on Telomerase Activity in Human Primary Hematopoietic Cells from Patients with Dyskeratosis Congenita.
Vieri M; Kirschner M; Tometten M; Abels A; Rolles B; Isfort S; Panse J; Brümmendorf TH; Beier F
Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 33003434
[TBL] [Abstract][Full Text] [Related]
17. Dyskeratosis congenita--two siblings with a new missense mutation in the DKC1 gene.
Coelho JD; Lestre S; Kay T; Lopes MJ; Fiadeiro T; Apetato M
Pediatr Dermatol; 2011; 28(4):464-6. PubMed ID: 21736606
[TBL] [Abstract][Full Text] [Related]
18. Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Vulliamy T; Marrone A; Szydlo R; Walne A; Mason PJ; Dokal I
Nat Genet; 2004 May; 36(5):447-9. PubMed ID: 15098033
[TBL] [Abstract][Full Text] [Related]
19. Pulmonary fibrosis in dyskeratosis congenita: report of 2 cases.
Dvorak LA; Vassallo R; Kirmani S; Johnson G; Hartman TE; Tazelaar HD; Leslie KO; Colby TV; Cockcroft DW; Churg AM; Yi ES
Hum Pathol; 2015 Jan; 46(1):147-52. PubMed ID: 25455995
[TBL] [Abstract][Full Text] [Related]
20. Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
Kanegane H; Kasahara Y; Okamura J; Hongo T; Tanaka R; Nomura K; Kojima S; Miyawaki T
Br J Haematol; 2005 May; 129(3):432-4. PubMed ID: 15842668
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]