ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.
<h4>Background</h4>Fibrillins 1 (FBN1) and 2 (FBN2) are components of microfibrils, microfilaments that are present in many connective tissues, either alone or in association with elastin. Marfan's syndrome and congenital contractural arachnodactyly (CCA) result from dominant mutati...
Enregistré dans:
Auteurs principaux: | Gaynor Miller, Monica Neilan, Ruth Chia, Nabeia Gheryani, Natalie Holt, Annabelle Charbit, Sara Wells, Valter Tucci, Zuzanne Lalanne, Paul Denny, Elizabeth M C Fisher, Michael Cheeseman, Graham N Askew, T Neil Dear |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Public Library of Science (PLoS)
2010
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/095c5bd1ac0c4528b8de42f504717eeb |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Cooperative Mechanism of ADAMTS/ ADAMTSL and Fibrillin-1 in the Marfan Syndrome and Acromelic Dysplasias
par: Pauline Arnaud, et autres
Publié: (2021) -
A Non-Rogue Mutant Line Induced by ENU Mutagenesis in Paramutated Rogue Peas (<i>Pisum sativum</i> L.) Is Still Sensitive to the Rogue Paramutation
par: Ricardo Pereira, et autres
Publié: (2021) -
Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database
par: Tao Wang, et autres
Publié: (2018) -
Mismatch repair-independent increase in spontaneous mutagenesis in yeast lacking non-essential subunits of DNA polymerase ε.
par: Anna Aksenova, et autres
Publié: (2010) -
Uracil Accumulation and Mutagenesis Dominated by Cytosine Deamination in CpG Dinucleotides in Mice Lacking UNG and SMUG1
par: Lene Alsøe, et autres
Publié: (2017)