Novel insights into fibrillin-1 and TGFβ contributions to aortic disease in Marfan syndrome

被引：0
|
作者：
Cook, Jason [1 ]
Carta, Luca [1 ]
del Solar, Maria [1 ]
Lindsay, Mark [2 ]
Dietz, Harry [2 ]
Ramirez, Francesco [1 ]
机构：
[1] Mt Sinai Sch Med, New York, NY USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
来源：
GLYCOBIOLOGY | 2012年 / 22卷 / 11期
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：1558 / 1558
页数：1
相关论文
共 50 条
  • [1] Aortic dilatation in Marfan syndrome: role of arterial stiffness and fibrillin-1 variants
    Salvi, Paolo
    Grillo, Andrea
    Marelli, Susan
    Gao, Lan
    Salvi, Lucia
    Viecca, Maurizio
    Di Blasio, Anna Maria
    Carretta, Renzo
    Pini, Alessandro
    Parati, Gianfranco
    JOURNAL OF HYPERTENSION, 2018, 36 (01) : 77 - 84
  • [2] A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome
    Kochilas, L.
    Gundogan, F.
    Atalay, M.
    Bliss, J. M.
    Vatta, M.
    Pena, L. S.
    Abuelo, D.
    JOURNAL OF PERINATOLOGY, 2008, 28 (04) : 303 - 305
  • [3] A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome
    L Kochilas
    F Gundogan
    M Atalay
    J M Bliss
    M Vatta
    L S Pena
    D Abuelo
    Journal of Perinatology, 2008, 28 : 303 - 305
  • [4] Novel frameshift mutations in fibrillin-1 gene causing Marfan syndrome
    Gusina, A.
    Miasnikov, S.
    Gusina, N.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 914 - 914
  • [5] Fibrillin-1 gene mutations are predictors of marfan syndrome
    Zhang, Lin
    Zhou, Xianliang
    Gao, Linggen
    Hui, Rutai
    CARDIOLOGY, 2011, 120 : 53 - 54
  • [6] Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndrome
    Ganesh, A
    Smith, C
    Chan, W
    Unger, S
    Quercia, N
    Godfrey, M
    Kraft, S
    Buncic, R
    Levin, A
    ARCHIVES OF OPHTHALMOLOGY, 2006, 124 (02) : 205 - 209
  • [7] A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in a Korean Girl
    Nam, Hyo-Kyoung
    Nam, Myung-Hyun
    Ha, Kee-Soo
    Rhie, Young-Jun
    Lee, Kee-Hyoung
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2017, 47 (02): : 221 - 225
  • [8] A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in Korean Girl
    Nam, Hyo-Kyoung
    Nam, Myung-Hyun
    Rhie, Young-Jun
    Lee, Kee-Hyoung
    HORMONE RESEARCH IN PAEDIATRICS, 2016, 86 : 462 - 462
  • [9] Six novel mutations of the fibrillin-1 gene in Korean patients with Marfan syndrome
    Oh, MR
    Kim, JS
    Beck, NS
    Lee, HJ
    Kohsaka, T
    Jin, DK
    PEDIATRICS INTERNATIONAL, 2000, 42 (05) : 488 - 491
  • [10] A novel mutation in fibrillin-1 gene identified in a Chinese family with marfan syndrome
    Liu, Dan-Li
    Cao, Juan-Hui
    Yang, Jie
    He, Fen
    Wang, Yun
    Fan, Ning
    Liu, Xu-Yang
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (05): : 7419 - 7424
12345