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An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis.
Published in:
Molecular Syndromology, 2019, v. 10, n. 1/2, p. 98, doi. 10.1159/000491567
By:
- Seda, Marian;
- Geerlings, Maartje;
- Lim, Peggy;
- Jeyabalan-Srikaran, Jeshmi;
- Cichon, ann-Christin;
- Scambler, Peter J.;
- Beales, Philip L.;
- Hernandez-Hernandez, Victor;
- Stoker, andrew W.;
- Jenkins, Dagan
Publication type:
Article
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis.
Published in:
Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33589-y
By:
- Seda, Marian;
- Crespo, Berta;
- Corcelli, Michelangelo;
- Osborn, Daniel P.;
- Jenkins, Dagan
Publication type:
Article
Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transport.
Published in:
EMBO Journal, 2024, v. 43, n. 7, p. 1257, doi. 10.1038/s44318-024-00060-1
By:
- Mukhopadhyay, Aakash G;
- Toropova, Katerina;
- Daly, Lydia;
- Wells, Jennifer N;
- Vuolo, Laura;
- Mladenov, Miroslav;
- Seda, Marian;
- Jenkins, Dagan;
- Stephens, David J;
- Roberts, Anthony J
Publication type:
Article
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70797-2
By:
- Bryant, Dale;
- Seda, Marian;
- Peskett, Emma;
- Maurer, Constance;
- Pomeranz, Gideon;
- Ghosh, Marcus;
- Hawkins, Thomas A.;
- Cleak, James;
- Datta, Sanchari;
- Hariri, Hanaa;
- Eckert, Kaitlyn M.;
- Jafree, Daniyal J.;
- Walsh, Claire;
- Demetriou, Charalambos;
- Ishida, Miho;
- Alemán-Charlet, Cristina;
- Vestito, Letizia;
- Seselgyte, Rimante;
- McDonald, Jeffrey G.;
- Bitner-Glindzicz, Maria
Publication type:
Article
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.
Published in:
Human Molecular Genetics, 2018, v. 27, n. 11, p. 1927, doi. 10.1093/hmg/ddy101
By:
- Bryant, Dale;
- Yang Liu;
- Datta, Sanchari;
- Hariri, Hanaa;
- Seda, Marian;
- Anderson, Glenn;
- Peskett, Emma;
- Demetriou, Charalambos;
- Sousa, Sergio;
- Jenkins, Dagan;
- Clayton, Peter;
- Bitner-Glindzicz, Maria;
- Moore, Gudrun E.;
- Henne, W. Mike;
- Stanier, Philip
Publication type:
Article
De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of Bbs1.
Published in:
Cells (2073-4409), 2023, v. 12, n. 22, p. 2662, doi. 10.3390/cells12222662
By:
- Freke, Grace Mercedes;
- Martins, Tiago;
- Davies, Rosalind Jane;
- Beyer, Tina;
- Seda, Marian;
- Peskett, Emma;
- Haq, Naila;
- Prasai, Avishek;
- Otto, Georg;
- Jeyabalan Srikaran, Jeshmi;
- Hernandez, Victor;
- Diwan, Gaurav D.;
- Russell, Robert B.;
- Ueffing, Marius;
- Huranova, Martina;
- Boldt, Karsten;
- Beales, Philip L.;
- Jenkins, Dagan
Publication type:
Article

Found: 6

An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis.

A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis.

Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transport.

Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.

SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.

De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of Bbs1.