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Maternal iron deficiency perturbs embryonic cardiovascular development in mice.
Published in:
Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23660-5
By:
- Kalisch-Smith, Jacinta I.;
- Ved, Nikita;
- Szumska, Dorota;
- Munro, Jacob;
- Troup, Michael;
- Harris, Shelley E.;
- Rodriguez-Caro, Helena;
- Jacquemot, Aimée;
- Miller, Jack J.;
- Stuart, Eleanor M.;
- Wolna, Magda;
- Hardman, Emily;
- Prin, Fabrice;
- Lana-Elola, Eva;
- Aoidi, Rifdat;
- Fisher, Elizabeth M. C.;
- Tybulewicz, Victor L. J.;
- Mohun, Timothy J.;
- Lakhal-Littleton, Samira;
- De Val, Sarah
Publication type:
Article
Functional redundancy of the kinases MEK1 and MEK2: Rescue of the Mek1 mutant phenotype by Mek2 knock-in reveals a protein threshold effect.
Published in:
Science Signaling, 2016, v. 9, n. 412, p. 1, doi. 10.1126/scisignal.aad5658
By:
- Aoidi, Rifdat;
- Maltais, Annie;
- Charron, Jean
Publication type:
Article
Lung development requires an active ERK/MAPK pathway in the lung mesenchyme.
Published in:
Developmental Dynamics, 2017, v. 246, n. 1, p. 72, doi. 10.1002/dvdy.24464
By:
- Boucherat, Olivier;
- Landry‐Truchon, Kim;
- Aoidi, Rifdat;
- Houde, Nicolas;
- Nadeau, Valérie;
- Charron, Jean;
- Jeannotte, Lucie
Publication type:
Article
OCRL-mutated fibroblasts from patients with Dent-2 disease exhibit INPP5B-independent phenotypic variability relatively to Lowe syndrome cells.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 4, p. 994, doi. 10.1093/hmg/ddu514
By:
- Montjean, Rodrick;
- Aoidi, Rifdat;
- Desbois, Pierrette;
- Rucci, Julien;
- Trichet, Michaël;
- Salomon, Rémi;
- Rendu, John;
- Fauré, Julien;
- Lunardi, Joël;
- Gacon, Gérard;
- Billuart, Pierre;
- Dorseuil, Olivier
Publication type:
Article
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome.
Published in:
Science Translational Medicine, 2024, v. 16, n. 731, p. 1, doi. 10.1126/scitranslmed.add6883
By:
- Lana-Elola, Eva;
- Aoidi, Rifdat;
- Llorian, Miriam;
- Gibbins, Dorota;
- Buechsenschuetz, Callan;
- Bussi, Claudio;
- Flynn, Helen;
- Gilmore, Tegan;
- Watson-Scales, Sheona;
- Haugsten Hansen, Marie;
- Hayward, Darryl;
- Song, Ok-Ryul;
- Brault, Véronique;
- Herault, Yann;
- Deau, Emmanuel;
- Meijer, Laurent;
- Snijders, Ambrosius P.;
- Gutierrez, Maximiliano G.;
- Fisher, Elizabeth M. C.;
- Tybulewicz, Victor L. J.
Publication type:
Article

Found: 5

Maternal iron deficiency perturbs embryonic cardiovascular development in mice.

Functional redundancy of the kinases MEK1 and MEK2: Rescue of the Mek1 mutant phenotype by Mek2 knock-in reveals a protein threshold effect.

Lung development requires an active ERK/MAPK pathway in the lung mesenchyme.

OCRL-mutated fibroblasts from patients with Dent-2 disease exhibit INPP5B-independent phenotypic variability relatively to Lowe syndrome cells.

Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome.