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Items: 1 to 20 of 32

1.

Nonradioactive detection of telomerase activity using the telomeric repeat amplification protocol.

Herbert BS, Hochreiter AE, Wright WE, Shay JW.

Nat Protoc. 2006;1(3):1583-90.

PMID:
17406450
2.

Incidence and prevalence of idiopathic pulmonary fibrosis.

Raghu G, Weycker D, Edelsberg J, Bradford WZ, Oster G.

Am J Respir Crit Care Med. 2006 Oct 1;174(7):810-6. Epub 2006 Jun 29.

PMID:
16809633
3.

Telomere shortening in smokers with and without COPD.

Morlá M, Busquets X, Pons J, Sauleda J, MacNee W, Agustí AG.

Eur Respir J. 2006 Mar;27(3):525-8.

4.

High-dose acetylcysteine in idiopathic pulmonary fibrosis.

Demedts M, Behr J, Buhl R, Costabel U, Dekhuijzen R, Jansen HM, MacNee W, Thomeer M, Wallaert B, Laurent F, Nicholson AG, Verbeken EK, Verschakelen J, Flower CD, Capron F, Petruzzelli S, De Vuyst P, van den Bosch JM, Rodriguez-Becerra E, Corvasce G, Lankhorst I, Sardina M, Montanari M; IFIGENIA Study Group.

N Engl J Med. 2005 Nov 24;353(21):2229-42.

5.

Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.

Armanios M, Chen JL, Chang YP, Brodsky RA, Hawkins A, Griffin CA, Eshleman JR, Cohen AR, Chakravarti A, Hamosh A, Greider CW.

Proc Natl Acad Sci U S A. 2005 Nov 1;102(44):15960-4. Epub 2005 Oct 24.

6.

Clinical and pathologic features of familial interstitial pneumonia.

Steele MP, Speer MC, Loyd JE, Brown KK, Herron A, Slifer SH, Burch LH, Wahidi MM, Phillips JA 3rd, Sporn TA, McAdams HP, Schwarz MI, Schwartz DA.

Am J Respir Crit Care Med. 2005 Nov 1;172(9):1146-52. Epub 2005 Aug 18.

7.

Identification and functional characterization of 2 variant alleles of the telomerase RNA template gene (TERC) in a patient with dyskeratosis congenita.

Ly H, Schertzer M, Jastaniah W, Davis J, Yong SL, Ouyang Q, Blackburn EH, Parslow TG, Lansdorp PM.

Blood. 2005 Aug 15;106(4):1246-52. Epub 2005 May 10.

8.

Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.

Yamaguchi H, Calado RT, Ly H, Kajigaya S, Baerlocher GM, Chanock SJ, Lansdorp PM, Young NS.

N Engl J Med. 2005 Apr 7;352(14):1413-24.

9.

ELXR: a resource for rapid exon-directed sequence analysis.

Schageman JJ, Horton CJ, Niu S, Garner HR, Pertsemlidis A.

Genome Biol. 2004;5(5):R36. Epub 2004 Apr 28.

10.

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. Epub 2004 Apr 18.

PMID:
15098033
11.

Template boundary definition in mammalian telomerase.

Chen JL, Greider CW.

Genes Dev. 2003 Nov 15;17(22):2747-52.

12.

Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA.

Fogarty PF, Yamaguchi H, Wiestner A, Baerlocher GM, Sloand E, Zeng WS, Read EJ, Lansdorp PM, Young NS.

Lancet. 2003 Nov 15;362(9396):1628-30.

PMID:
14630445
13.

Oxidative stress shortens telomeres.

von Zglinicki T.

Trends Biochem Sci. 2002 Jul;27(7):339-44.

PMID:
12114022
14.

Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.

Thomas AQ, Lane K, Phillips J 3rd, Prince M, Markin C, Speer M, Schwartz DA, Gaddipati R, Marney A, Johnson J, Roberts R, Haines J, Stahlman M, Loyd JE.

Am J Respir Crit Care Med. 2002 May 1;165(9):1322-8.

PMID:
11991887
16.

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Abecasis GR, Cherny SS, Cookson WO, Cardon LR.

Nat Genet. 2002 Jan;30(1):97-101. Epub 2001 Dec 3.

PMID:
11731797
17.
18.

The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.

Vulliamy T, Marrone A, Goldman F, Dearlove A, Bessler M, Mason PJ, Dokal I.

Nature. 2001 Sep 27;413(6854):432-5.

PMID:
11574891
19.

Idiopathic pulmonary fibrosis.

Gross TJ, Hunninghake GW.

N Engl J Med. 2001 Aug 16;345(7):517-25. Review.

20.

A mutation in the surfactant protein C gene associated with familial interstitial lung disease.

Nogee LM, Dunbar AE 3rd, Wert SE, Askin F, Hamvas A, Whitsett JA.

N Engl J Med. 2001 Feb 22;344(8):573-9. No abstract available.

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