Results 181 to 190 of about 20,277 (271)

Combined ADAMTS10 and ADAMTS17 inactivation exacerbates bone shortening and skin phenotypes. [PDF]

Life Sci Alliance
Taye N, Karoulias SZ, Balic Z, Wang LW, Willard BB, Martin D, Richard D, Okamoto AS, Capellini TD, Apte SS, Hubmacher D.   +10 more
europepmc   +1 more source

Elastin haploinsufficiency induces alternative aging processes in the aorta [PDF]

, 2008
Boyle, Walter A, Escoubet, Brigitte, Faury, Gilles, Gheduzzi, Dealba, Huber, Philippe, Jacob, Marie-Paule, Li, Dean Y, Mecham, Robert P, Perret, Pascale, Pezet, Mylène, Quaglino, Daniela, Starcher, Barry, Tillet, Emmanuelle, Vranckx, Roger   +13 more
core   +2 more sources

Exploring thoracic aorta ECM alterations in Marfan syndrome: insights into aorta wall structure. [PDF]

Sci Rep
de Souza RB, Cassiano LL, Barnowski P, Ventura S, Turato WM, Nascimento SCR, Mignanelli GL, Caldeira W, da Fonseca Martins AMCRP, de Carvalho Luposeli F, Laurindo FRM, Reinhardt DP, Sengle G, Koh IHJ, Meek KM, Lewis PN.   +15 more
europepmc   +1 more source

Common polymorphisms of Fibulin-5 and the risk of abdominal aortic aneurysm development [PDF]

, 2010
Badger, Stephen A., Hughes, Anne E., Makar, Ragai R., O'Donnell, Mark E., Sharif, Mohammed A., Soong, Chee V.   +5 more
core   +1 more source

Identification of a Major Microfibril-associated Glycoprotein-1-binding Domain in Fibrillin-2 [PDF]

, 2004
Cláudio C. Werneck, Barbara Crippes Trask, Thomas J. Broekelmann, Timothy M. Trask, Timothy M. Ritty, Fernando Segade, Robert P. Mecham   +6 more
openalex   +1 more source

Fibrillin-1 mutation contributes to Marfan syndrome by inhibiting Cav1.2-mediated cell proliferation in vascular smooth muscle cells

, 2023
Wenfeng Lin, Jiaqi Xiong, Yefan Jiang, Hao Liu, Jinhui Bian, Juejin Wang, Yongfeng Shao, Buqing Ni   +7 more
openalex   +1 more source

Transforming growth factor-beta (TGF-β) in the pathogenesis of hereditary thoracic aneurysm disorders. [PDF]

Cardiovasc Pathol
Espinoza Camejo WA, Bramel EE, MacFarlane EG.   +2 more
europepmc   +1 more source

Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations [PDF]

, 2002
Kathrin Rommel, Matthias Karck, Axel Haverich, Jörg Schmidtke, Mine Arslan‐Kirchner   +4 more
openalex   +1 more source

Immunohistochemical expression of fibrillin-1 and fibrillin-2 during tooth development.

Immunohistochemical expression of fibrillin-1 and fibrillin-2 during tooth development.
BACKGROUND AND OBJECTIVE: Oxytalan fibers are categorized as a microfibril assembly without elastin deposition, and are unique components in the periodontal ligament (PDL). However, little is known about their formation during PDL development. To clarify the mechanisms of oxytalan fiber formation in developing PDL, we performed immunohistochemical ...
openaire  

Gestational diabetes alters prefrontal neurochemistry and disrupts maternal behaviors: Role of Fibrillin-1, serotonin, and TNF-α in rats. [PDF]

Metabol Open
Khayat S, Fanaei H, Safarzaei A.
europepmc   +1 more source