BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 37834388)

  • 21. Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes.
    Kalejaiye A; Giri N; Brewer CC; Zalewski CK; King KA; Adams CD; Rosenberg PS; Kim HJ; Alter BP
    Pediatr Blood Cancer; 2016 Dec; 63(12):2139-2145. PubMed ID: 27428025
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita.
    Tsilou ET; Giri N; Weinstein S; Mueller C; Savage SA; Alter BP
    Ophthalmology; 2010 Mar; 117(3):615-22. PubMed ID: 20022637
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Dangerous liaisons: p53, dyskeratosis congenita and Fanconi anemia].
    Toufektchan E; Jaber S; Toledo F
    Med Sci (Paris); 2017 Jan; 33(1):95-98. PubMed ID: 28120765
    [No Abstract]   [Full Text] [Related]  

  • 24. A zebrafish model of dyskeratosis congenita reveals hematopoietic stem cell formation failure resulting from ribosomal protein-mediated p53 stabilization.
    Pereboom TC; van Weele LJ; Bondt A; MacInnes AW
    Blood; 2011 Nov; 118(20):5458-65. PubMed ID: 21921046
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Inherited bone marrow failure syndromes in 2012.
    Sakaguchi H; Nakanishi K; Kojima S
    Int J Hematol; 2013 Jan; 97(1):20-9. PubMed ID: 23271412
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Immune status of patients with inherited bone marrow failure syndromes.
    Giri N; Alter BP; Penrose K; Falk RT; Pan Y; Savage SA; Williams M; Kemp TJ; Pinto LA
    Am J Hematol; 2015 Aug; 90(8):702-8. PubMed ID: 25963299
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
    Alter BP; Giri N; Savage SA; Peters JA; Loud JT; Leathwood L; Carr AG; Greene MH; Rosenberg PS
    Br J Haematol; 2010 Jul; 150(2):179-88. PubMed ID: 20507306
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
    Ballew BJ; Yeager M; Jacobs K; Giri N; Boland J; Burdett L; Alter BP; Savage SA
    Hum Genet; 2013 Apr; 132(4):473-80. PubMed ID: 23329068
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [New insights into inherited bone marrow failure syndrome].
    Ito E; Toki T; Kamio T; Terui K
    Rinsho Ketsueki; 2021; 62(10):1455-1464. PubMed ID: 34732617
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy.
    Gramatges MM; Bertuch AA
    Transl Res; 2013 Dec; 162(6):353-63. PubMed ID: 23732052
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Severity of X-linked dyskeratosis congenita (DKCX) cellular defects is not directly related to dyskerin (DKC1) activity in ribosomal RNA biogenesis or mRNA translation.
    Thumati NR; Zeng XL; Au HH; Jang CJ; Jan E; Wong JM
    Hum Mutat; 2013 Dec; 34(12):1698-707. PubMed ID: 24115260
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutant mice lacking the p53 C-terminal domain model telomere syndromes.
    Simeonova I; Jaber S; Draskovic I; Bardot B; Fang M; Bouarich-Bourimi R; Lejour V; Charbonnier L; Soudais C; Bourdon JC; Huerre M; Londono-Vallejo A; Toledo F
    Cell Rep; 2013 Jun; 3(6):2046-58. PubMed ID: 23770245
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dyskeratosis congenita and telomerase.
    Bessler M; Wilson DB; Mason PJ
    Curr Opin Pediatr; 2004 Feb; 16(1):23-8. PubMed ID: 14758110
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromes.
    Alter BP; Rosenberg PS; Day T; Menzel S; Giri N; Savage SA; Thein SL
    Br J Haematol; 2013 Aug; 162(4):542-6. PubMed ID: 23713742
    [TBL] [Abstract][Full Text] [Related]  

  • 35. De novo TP53 germline activating mutations in two patients with the phenotype mimicking Diamond-Blackfan anemia.
    Fedorova D; Ovsyannikova G; Kurnikova M; Pavlova A; Konyukhova T; Pshonkin A; Smetanina N
    Pediatr Blood Cancer; 2022 Apr; 69(4):e29558. PubMed ID: 35084091
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway.
    Antunes AT; Goos YJ; Pereboom TC; Hermkens D; Wlodarski MW; Da Costa L; MacInnes AW
    PLoS Genet; 2015 Jul; 11(7):e1005326. PubMed ID: 26132763
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Telomere dynamics and hematopoietic differentiation of human DKC1-mutant induced pluripotent stem cells.
    Donaires FS; Alves-Paiva RM; Gutierrez-Rodrigues F; da Silva FB; Tellechea MF; Moreira LF; Santana BA; Traina F; Dunbar CE; Winkler T; Calado RT
    Stem Cell Res; 2019 Oct; 40():101540. PubMed ID: 31479877
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Zebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processing.
    Zhang Y; Morimoto K; Danilova N; Zhang B; Lin S
    PLoS One; 2012; 7(1):e30188. PubMed ID: 22299032
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dyskeratosis congenita as a disorder of telomere maintenance.
    Nelson ND; Bertuch AA
    Mutat Res; 2012 Feb; 730(1-2):43-51. PubMed ID: 21745483
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish.
    Yadav GV; Chakraborty A; Uechi T; Kenmochi N
    Int J Biochem Cell Biol; 2014 Apr; 49():1-7. PubMed ID: 24417973
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.