BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 27879313)

  • 21. A novel mutation of TGFBR2 causing Loeys-Dietz syndrome complicated with pregnancy-related fatal cervical arterial dissections.
    Fujita D; Takeda N; Morita H; Kato M; Nishimura H; Inuzuka R; Taniguchi Y; Nawata K; Hyodo H; Imai Y; Hirata Y; Komuro I
    Int J Cardiol; 2015 Dec; 201():288-90. PubMed ID: 26301661
    [No Abstract]   [Full Text] [Related]  

  • 22. Loeys-Dietz syndrome.
    Van Laer L; Dietz H; Loeys B
    Adv Exp Med Biol; 2014; 802():95-105. PubMed ID: 24443023
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects.
    Disabella E; Grasso M; Marziliano N; Ansaldi S; Lucchelli C; Porcu E; Tagliani M; Pilotto A; Diegoli M; Lanzarini L; Malattia C; Pelliccia A; Ficcadenti A; Gabrielli O; Arbustini E
    Eur J Hum Genet; 2006 Jan; 14(1):34-8. PubMed ID: 16251899
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel TGFBR2 and known missense SMAD3 mutations: two case reports of thoracic aortic aneurysms.
    Panesi P; Foffa I; Sabina S; Ait Ali L; Andreassi MG
    Ann Thorac Surg; 2015 Jan; 99(1):303-5. PubMed ID: 25555948
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification and surgical repair of familial thoracic aortic aneurysm and dissection caused by TGFBR1 mutation.
    Dong SB; Zheng J; Ma WG; Chen MJ; Cheng LJ; He L; Xing QH; Sun LZ
    Ann Vasc Surg; 2014 Nov; 28(8):1909-12. PubMed ID: 25110237
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of the TGF-beta receptor genes with abdominal aortic aneurysm.
    Baas AF; Medic J; van 't Slot R; de Kovel CG; Zhernakova A; Geelkerken RH; Kranendonk SE; van Sterkenburg SM; Grobbee DE; Boll AP; Wijmenga C; Blankensteijn JD; Ruigrok YM
    Eur J Hum Genet; 2010 Feb; 18(2):240-4. PubMed ID: 19672284
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Marfan syndrome type II: there is more to Marfan syndrome than fibrillin 1.
    Zangwill SD; Brown MD; Bryke CR; Cava JR; Segura AD
    Congenit Heart Dis; 2006 Sep; 1(5):229-32. PubMed ID: 18377530
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Associations of TGFBR1 and TGFBR2 gene polymorphisms with the risk of hypospadias: a case-control study in a Chinese population.
    Han XR; Wen X; Wang S; Hong XW; Fan SH; Zhuang J; Wang YJ; Zhang ZF; Li MQ; Hu B; Shan Q; Sun CH; Bao YX; Lin M; He T; Wu DM; Lu J; Zheng YL
    Biosci Rep; 2017 Oct; 37(5):. PubMed ID: 28894026
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new locus-specific database (LSDB) for mutations in the TGFBR2 gene: UMD-TGFBR2.
    Frederic MY; Hamroun D; Faivre L; Boileau C; Jondeau G; Claustres M; Béroud C; Collod-Béroud G
    Hum Mutat; 2008 Jan; 29(1):33-8. PubMed ID: 17935258
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension.
    Schievink WI; Gordon OK; Hyland JC; Ala-Kokko L
    J Headache Pain; 2008 Apr; 9(2):99-102. PubMed ID: 18264665
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation.
    Sheikhzadeh S; Brockstaedt L; Habermann CR; Sondermann C; Bannas P; Mir TS; Staebler A; Seidel H; Keyser B; Arslan-Kirchner M; Kutsche K; Berger J; Blankenberg S; von Kodolitsch Y
    Clin Genet; 2014 Dec; 86(6):545-51. PubMed ID: 24344637
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations.
    Söylen B; Singh KK; Abuzainin A; Rommel K; Becker H; Arslan-Kirchner M; Schmidtke J
    Clin Genet; 2009 Mar; 75(3):265-70. PubMed ID: 19159394
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome.
    Viassolo V; Lituania M; Marasini M; Dietz H; Benelli F; Forzano F; Faravelli F
    Prenat Diagn; 2006 Nov; 26(11):1081-3. PubMed ID: 16981219
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse.
    Aalberts JJ; van Tintelen JP; Oomen T; Bergman JE; Halley DJ; Jongbloed JD; Suurmeijer AJ; van den Berg MP
    Am J Med Genet A; 2014 Jan; 164A(1):113-9. PubMed ID: 24243761
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections.
    Pannu H; Fadulu VT; Chang J; Lafont A; Hasham SN; Sparks E; Giampietro PF; Zaleski C; Estrera AL; Safi HJ; Shete S; Willing MC; Raman CS; Milewicz DM
    Circulation; 2005 Jul; 112(4):513-20. PubMed ID: 16027248
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Early surgical experience with Loeys-Dietz: a new syndrome of aggressive thoracic aortic aneurysm disease.
    Williams JA; Loeys BL; Nwakanma LU; Dietz HC; Spevak PJ; Patel ND; François K; DeBacker J; Gott VL; Vricella LA; Cameron DE
    Ann Thorac Surg; 2007 Feb; 83(2):S757-63; discussion S785-90. PubMed ID: 17257922
    [TBL] [Abstract][Full Text] [Related]  

  • 37. ACE and TGFBR1 genes interact in influencing the susceptibility to abdominal aortic aneurysm.
    Lucarini L; Sticchi E; Sofi F; Pratesi G; Pratesi C; Pulli R; Gensini GF; Abbate R; Pepe G; Fatini C
    Atherosclerosis; 2009 Jan; 202(1):205-10. PubMed ID: 18550062
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Quantitative analysis of TGFBR2 mutations in Marfan-syndrome-related disorders suggests a correlation between phenotypic severity and Smad signaling activity.
    Horbelt D; Guo G; Robinson PN; Knaus P
    J Cell Sci; 2010 Dec; 123(Pt 24):4340-50. PubMed ID: 21098638
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Concordant promoter methylation of transforming growth factor-beta receptor types I and II occurs early in esophageal squamous cell carcinoma.
    Dong Z; Guo W; Guo Y; Kuang G; Yang Z
    Am J Med Sci; 2012 May; 343(5):375-81. PubMed ID: 22314103
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Downregulation of transforming growth factor, beta receptor 2 and Notch signaling pathway in human abdominal aortic aneurysm.
    Biros E; Walker PJ; Nataatmadja M; West M; Golledge J
    Atherosclerosis; 2012 Apr; 221(2):383-6. PubMed ID: 22310065
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.