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...
Prif Awdur: | Iqbal, S |
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Awduron Eraill: | Handford, P |
Fformat: | Traethawd Ymchwil |
Iaith: | English |
Cyhoeddwyd: |
2011
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Pynciau: |
Eitemau Tebyg
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Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
gan: Loeys, B, et al.
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gan: Robertson, I, et al.
Cyhoeddwyd: (2012) -
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gan: Yadin, D
Cyhoeddwyd: (2013) -
A combined bioinformatics and experimental approach towards the molecular phenotype of disease-causing single point mutations.
gan: Lim, Radiance Hui Ting.
Cyhoeddwyd: (2010) -
Biochemistry and molecular biology compendium /
gan: 340867 Lundblad, Roger L.
Cyhoeddwyd: (c200)