Frederic Castinetti (Qing Fang)

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 3

Top Topics

Epithelial Mesenchymal Transition

Spectrum Disorder

Binding Protein

Top Venues

European journal of endocrinology

Human molecular genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Hironori Bando, Michelle L Brinkmeier, Frederic Castinetti, Qing Fang, Mi-Sun Lee, Alexandru Saveanu, Frédérique Albarel, Clémentine Dupuis, Thierry Brue, Sally Ann Camper
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man. Human molecular genetics (2022)
Louise C Gregory, Peter Gergics, Marilena Nakaguma, Hironori Bando, Giuseppa Patti, Mark J McCabe, Frederic Castinetti, Qianyi Ma, Ayse Bilge Ozel, Jun Z Li, Michele Moreira Poina, Alexander Augusto de Lima Jorge, Anna F Figueredo Benedetti, Antonio M Lerario, Ivo J P Arnhold, Berenice Bilharinho de Mendonca, Mohamad Maghnie, Sally Ann Camper, Luciani R S Carvalho, Mehul T Dattani
The phenotypic spectrum associated with OTX2 mutations in humans. European journal of endocrinology 185 (1) (2021)
Frederic Castinetti, Artur A Indzhykulian, Mirna Mustapha, Gavin P Riordan, David F Dolan, Thomas B Friedman, Inna A Belyantseva, Gregory I Frolenkov, Sally A Camper, Jonathan E Bird
The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing. eLife 4 (2015)