Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Muthu L. Muthu"'
Publikováno v:
Adipocyte, Vol 13, Iss 1 (2024)
Introduction and Purpose Mouse mesenchymal stem cells (MSCs) provide a resourceful tool to study physiological and pathological aspects of adipogenesis. Bone marrow-derived MSCs (BM-MSCs) and adipose tissue-derived MSCs (ASCs) are widely used for the
Externí odkaz:
https://doaj.org/article/32781a21176a4fc0986ef24e17c23600
Publikováno v:
American journal of physiology. Cell physiology. 323(2)
Gene mutations in the extracellular matrix protein fibrillin-1 cause connective tissue disorders including Marfan syndrome (MFS) with clinical symptoms in the cardiovascular, skeletal, and ocular systems. Patients with MFS also exhibit alterations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925cd6464127c5e05c37cb88edf5a735
https://pubmed.ncbi.nlm.nih.gov/35759435
https://pubmed.ncbi.nlm.nih.gov/35759435
Autor:
Rong-Mo Zhang, Kerstin Tiedemann, Muthu L. Muthu, Neha E. H. Dinesh, Svetlana Komarova, Bhama Ramkhelawon, Dieter P. Reinhardt
Publikováno v:
Cellular and Molecular Life Sciences. 79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::290db35f03759b6bf638a7bb18f95538
https://doi.org/10.1007/s00018-022-04337-8
https://doi.org/10.1007/s00018-022-04337-8
Autor:
Muthu L. Muthu, Dieter P. Reinhardt
Publikováno v:
J Cell Commun Signal
The extracellular matrix microenvironment of adipose tissue is of critical importance for the differentiation, remodeling and function of adipocytes. Fibrillin-1 is one of the main components of microfibrils and a key player in this process. Furin pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9606ea65471c891084fa8feb739f3f19
https://doi.org/10.1007/s12079-020-00566-3
https://doi.org/10.1007/s12079-020-00566-3
Publikováno v:
Matrix biology : journal of the International Society for Matrix Biology. 110
Fibrillin-1 is an extracellular glycoprotein present throughout the body. Mutations in fibrillin-1 cause a wide spectrum of type I fibrillinopathies, including Marfan syndrome characterized by clinical manifestations in adipose tissues, among others.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac2c9b79dac5fb90240d32e11abedec
https://pubmed.ncbi.nlm.nih.gov/35533973
https://pubmed.ncbi.nlm.nih.gov/35533973