Molecular studies of stiff skin-causing mutations in fibrillin-1
<p>Fibrillin-1 is the main component of the 10-12 nm microfibrils, which are found in several elastic and non-elastic tissues. Human fibrillin-1 contains multiple calcium-binding epidermal growth factor-like (cbEGF) domains interspersed with transforming growth factor β-binding protein-like (T...
Hlavní autor: | Iqbal, S |
---|---|
Další autoři: | Handford, P |
Médium: | Diplomová práce |
Jazyk: | English |
Vydáno: |
2011
|
Témata: |
Podobné jednotky
-
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
Autor: Loeys, B, a další
Vydáno: (2010) -
An investigation into the molecular mechanism of the fibrillin1 - LTBP1 interaction
Autor: Robertson, I, a další
Vydáno: (2012) -
Molecular and structural characterisation of the human Fibrillin-1 N-C terminal interaction
Autor: Yadin, D
Vydáno: (2013) -
A combined bioinformatics and experimental approach towards the molecular phenotype of disease-causing single point mutations.
Autor: Lim, Radiance Hui Ting.
Vydáno: (2010) -
Biochemistry and molecular biology compendium /
Autor: 340867 Lundblad, Roger L.
Vydáno: (c200)