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 *

143 related articles for article (PubMed ID: 12621102)

  • 1. Insights into the genetic and molecular basis of primary pulmonary hypertension.
    Trembath RC; Harrison R
    Pediatr Res; 2003 Jun; 53(6):883-8. PubMed ID: 12621102
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel mutation in the gene for bone morphogenetic protein receptor II in an Israeli patient with familial primary pulmonary hypertension.
    Cahn A; Meiner V; Leitersdorf E; Berkman N
    Isr Med Assoc J; 2004 Mar; 6(3):156-9. PubMed ID: 15055271
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.
    Trembath RC; Thomson JR; Machado RD; Morgan NV; Atkinson C; Winship I; Simonneau G; Galie N; Loyd JE; Humbert M; Nichols WC; Morrell NW; Berg J; Manes A; McGaughran J; Pauciulo M; Wheeler L
    N Engl J Med; 2001 Aug; 345(5):325-34. PubMed ID: 11484689
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic basis of pulmonary arterial hypertension: current understanding and future directions.
    Newman JH; Trembath RC; Morse JA; Grunig E; Loyd JE; Adnot S; Coccolo F; Ventura C; Phillips JA; Knowles JA; Janssen B; Eickelberg O; Eddahibi S; Herve P; Nichols WC; Elliott G
    J Am Coll Cardiol; 2004 Jun; 43(12 Suppl S):33S-39S. PubMed ID: 15194176
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.
    Newman JH; Wheeler L; Lane KB; Loyd E; Gaddipati R; Phillips JA; Loyd JE
    N Engl J Med; 2001 Aug; 345(5):319-24. PubMed ID: 11484688
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mutations of genes coding for TGF-beta receptors (BMPR2 and ALK-1) in primary pulmonary arterial hypertension].
    Humbert M
    J Soc Biol; 2002; 196(1):53-8. PubMed ID: 12134634
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension.
    Machado RD; Rudarakanchana N; Atkinson C; Flanagan JA; Harrison R; Morrell NW; Trembath RC
    Hum Mol Genet; 2003 Dec; 12(24):3277-86. PubMed ID: 14583445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family.
    Thomson JR; Machado RD; Pauciulo MW; Morgan NV; Humbert M; Elliott GC; Ward K; Yacoub M; Mikhail G; Rogers P; Newman J; Wheeler L; Higenbottam T; Gibbs JS; Egan J; Crozier A; Peacock A; Allcock R; Corris P; Loyd JE; Trembath RC; Nichols WC
    J Med Genet; 2000 Oct; 37(10):741-5. PubMed ID: 11015450
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.
    Machado RD; Aldred MA; James V; Harrison RE; Patel B; Schwalbe EC; Gruenig E; Janssen B; Koehler R; Seeger W; Eickelberg O; Olschewski H; Elliott CG; Glissmeyer E; Carlquist J; Kim M; Torbicki A; Fijalkowska A; Szewczyk G; Parma J; Abramowicz MJ; Galie N; Morisaki H; Kyotani S; Nakanishi N; Morisaki T; Humbert M; Simonneau G; Sitbon O; Soubrier F; Coulet F; Morrell NW; Trembath RC
    Hum Mutat; 2006 Feb; 27(2):121-32. PubMed ID: 16429395
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic clues to the cause of primary pulmonary hypertension.
    Loscalzo J
    N Engl J Med; 2001 Aug; 345(5):367-71. PubMed ID: 11484696
    [No Abstract]   [Full Text] [Related]  

  • 11. Genetics of pulmonary hypertension: from bench to bedside.
    Humbert M; Trembath RC
    Eur Respir J; 2002 Sep; 20(3):741-9. PubMed ID: 12358355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pulling apart pulmonary hypertension.
    Scott J
    Nat Genet; 2000 Sep; 26(1):3-4. PubMed ID: 10973231
    [No Abstract]   [Full Text] [Related]  

  • 13. [Clinical and genetic characteristics of a Chinese family of primary pulmonary hypertension].
    Jing ZC; Lu LH; Zou YB; You SJ; Han ZY; Zhang Q; Yang YJ; Hui RT; Cheng XS
    Zhonghua Yi Xue Za Zhi; 2004 Feb; 84(3):199-202. PubMed ID: 15059534
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pulmonary hypertension in scleroderma spectrum of disease: lack of bone morphogenetic protein receptor 2 mutations.
    Morse J; Barst R; Horn E; Cuervo N; Deng Z; Knowles J
    J Rheumatol; 2002 Nov; 29(11):2379-81. PubMed ID: 12415595
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Signaling molecules in nonfamilial pulmonary hypertension.
    Du L; Sullivan CC; Chu D; Cho AJ; Kido M; Wolf PL; Yuan JX; Deutsch R; Jamieson SW; Thistlethwaite PA
    N Engl J Med; 2003 Feb; 348(6):500-9. PubMed ID: 12571257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dysfunctional Smad signaling contributes to abnormal smooth muscle cell proliferation in familial pulmonary arterial hypertension.
    Yang X; Long L; Southwood M; Rudarakanchana N; Upton PD; Jeffery TK; Atkinson C; Chen H; Trembath RC; Morrell NW
    Circ Res; 2005 May; 96(10):1053-63. PubMed ID: 15845886
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene for familial primary pulmonary hypertension identified.
    SoRelle R
    Circulation; 2000 Aug; 102(6):E9010-1. PubMed ID: 10950623
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel insertional mutation in the bone morphogenetic protein receptor type II associated with sporadic primary pulmonary hypertension.
    Sugiyama S; Hirota H; Yoshida M; Takemura Y; Nakaoka Y; Oshima Y; Terai K; Izumi M; Fujio Y; Hasegawa S; Mano T; Nakatsuchi Y; Hori M; Yamauchi-Takihara K; Kawase I
    Circ J; 2004 Jun; 68(6):592-4. PubMed ID: 15170098
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigation of second genetic hits at the BMPR2 locus as a modulator of disease progression in familial pulmonary arterial hypertension.
    Machado RD; James V; Southwood M; Harrison RE; Atkinson C; Stewart S; Morrell NW; Trembath RC; Aldred MA
    Circulation; 2005 Feb; 111(5):607-13. PubMed ID: 15699281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of pulmonary arterial hypertension: current and future implications.
    Elliott CG
    Semin Respir Crit Care Med; 2005 Aug; 26(4):365-71. PubMed ID: 16121312
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.