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 *

162 related articles for article (PubMed ID: 3909767)

  • 61. Increase in DNA synthesis in Werner's syndrome cells by hybridization with normal human diploid and HeLa cells.
    Tanaka K; Nakazawa T; Okada Y; Kumahara Y
    Exp Cell Res; 1979 Oct; 123(2):261-7. PubMed ID: 499358
    [No Abstract]   [Full Text] [Related]  

  • 62. Nailfold scleroderma-like capillary abnormalities in Werner syndrome (adult progeria).
    Ingegnoli F; Crotti C
    Vasc Med; 2017 Jun; 22(3):246-247. PubMed ID: 28466674
    [No Abstract]   [Full Text] [Related]  

  • 63. Werner syndrome: studies in an affected family reveal a cellular phenotype of unaffected siblings.
    Weirich HG; Weirich-Schwaiger H; Kofler H; Sidoroff A; Fritsch P; Schachtschabel DO; Schweiger M; Hirsch-Kauffmann M
    Mech Ageing Dev; 1996 Jul; 88(1-2):1-15. PubMed ID: 8803918
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Aging: progeria and the lamin connection.
    Kudlow BA; Kennedy BK
    Curr Biol; 2006 Aug; 16(16):R652-4. PubMed ID: 16920618
    [TBL] [Abstract][Full Text] [Related]  

  • 65. LMNA mutations in atypical Werner's syndrome.
    Bonne G; Levy N
    Lancet; 2003 Nov; 362(9395):1585-6; author reply 1586. PubMed ID: 14615129
    [No Abstract]   [Full Text] [Related]  

  • 66. [Hutchinson-Gilford-progeria syndrome as a cause of short stature].
    Zambrano RM; Rodríguez RB; Ariza LM
    An Pediatr (Barc); 2009 Sep; 71(3):273-5. PubMed ID: 19625224
    [No Abstract]   [Full Text] [Related]  

  • 67. Progeria, a model disease for the study of accelerated aging.
    Brown WT; Zebrower M; Kieras FJ
    Basic Life Sci; 1985; 35():375-96. PubMed ID: 4062819
    [No Abstract]   [Full Text] [Related]  

  • 68. Atypical meningioma in Werner syndrome: a case report.
    Marton E; Bonaldi L; Busato S; Longatti P
    J Neurooncol; 2006 Sep; 79(2):181-5. PubMed ID: 16598422
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Molecular bases of progeroid syndromes.
    Navarro CL; Cau P; Lévy N
    Hum Mol Genet; 2006 Oct; 15 Spec No 2():R151-61. PubMed ID: 16987878
    [TBL] [Abstract][Full Text] [Related]  

  • 70. [The human genome project and genomic analysis of progeroid syndromes].
    Nakura J
    Nihon Ronen Igakkai Zasshi; 2002 Jul; 39(4):372-4. PubMed ID: 12187795
    [No Abstract]   [Full Text] [Related]  

  • 71. Progeria (Hutchinson-Gilford): a case report.
    Sivaraman ; Thappa DM; D'Souza M; Ratnakar C
    J Dermatol; 1999 May; 26(5):324-8. PubMed ID: 10380434
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Progeroid syndromes].
    Nakura J
    Nihon Rinsho; 2002 Jan; 60 Suppl 1():601-6. PubMed ID: 11838172
    [No Abstract]   [Full Text] [Related]  

  • 73. Hip disease in Hutchinson-Gilford progeria syndrome.
    Gamble JG
    J Pediatr Orthop; 1984 Sep; 4(5):585-9. PubMed ID: 6490880
    [TBL] [Abstract][Full Text] [Related]  

  • 74. All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.
    Pellegrini C; Columbaro M; Capanni C; D'Apice MR; Cavallo C; Murdocca M; Lattanzi G; Squarzoni S
    Oncotarget; 2015 Oct; 6(30):29914-28. PubMed ID: 26359359
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Telomere length in Hutchinson-Gilford progeria syndrome.
    Decker ML; Chavez E; Vulto I; Lansdorp PM
    Mech Ageing Dev; 2009 Jun; 130(6):377-83. PubMed ID: 19428457
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Unstable enzymes in erythrocytes of a family with the Hutchinson--Gilford progeria syndrome.
    Goldstein S; Moerman EJ
    Prog Clin Biol Res; 1978; 21():217-31. PubMed ID: 662891
    [No Abstract]   [Full Text] [Related]  

  • 77. The premature ageing syndromes. Report of eight cases and description of a new entity named metageria.
    Gilkes JJ; Sharvill DE; Wells RS
    Br J Dermatol; 1974 Sep; 91(3):243-62. PubMed ID: 4447659
    [No Abstract]   [Full Text] [Related]  

  • 78. A population and cytogenetic study of the Werner syndrome in Sardinia.
    Fraccaro M; Scappaticci S; Cerimele D
    Adv Exp Med Biol; 1985; 190():547-52. PubMed ID: 4083163
    [No Abstract]   [Full Text] [Related]  

  • 79. Euploidization of human hepatocytes from donors of different ages and both sexes compared with those from cases of Werner's syndrome and progeria.
    Gahan PB; Middleton J
    Exp Gerontol; 1984; 19(6):355-8. PubMed ID: 6519207
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Molecular basis of the accumulation of abnormal proteins in progeria and aging fibroblasts.
    Gracy RW; Chapman ML; Cini JK; Jahani M; Tollefsbol TO; Yüksel KU
    Basic Life Sci; 1985; 35():427-42. PubMed ID: 4062822
    [No Abstract]   [Full Text] [Related]  

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