C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle

STIL Microcephaly Mutations Interfere with APC/C-Mediated Degradation and Cause Centriole Amplification

(2014) Christian Arquint et al.   CURRENT BIOLOGY

Multisite phosphorylation of C-Nap1 releases it from Cep135 to trigger centrosome disjunction

(2014) T. Hardy et al.   JOURNAL OF CELL SCIENCE

A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome

(2014) Samer Khateb et al.   JOURNAL OF MEDICAL GENETICS

Microtubules in Cell Migration

(2013) Sandrine Etienne-Manneville   Annual Review of Cell and Developmental Biology

EGF-Induced Centrosome Separation Promotes Mitotic Progression and Cell Survival

(2013) Balca R. Mardin et al.   DEVELOPMENTAL CELL

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function

(2012) Muhammad Sajid Hussain et al.   AMERICAN JOURNAL OF HUMAN GENETICS

C-NAP1 and rootletin restrain DNA damage-induced centriole splitting and facilitate ciliogenesis

(2012) Pauline C. Conroy et al.   CELL CYCLE

Breaking the ties that bind: New advances in centrosome biology

(2012) Balca R. Mardin et al.   JOURNAL OF CELL BIOLOGY

Concerted effort of centrosomal and Golgi-derived microtubules is required for proper Golgi complex assembly but not for maintenance

(2012) Tatiana Vinogradova et al.   MOLECULAR BIOLOGY OF THE CELL

The Centrosome in Cells and Organisms

(2012) M. Bornens   SCIENCE

Neural Crest Cell Lineage Restricts Skeletal Muscle Progenitor Cell Differentiation through Neuregulin1-ErbB3 Signaling

(2011) Andrew Tri Van Ho et al.   DEVELOPMENTAL CELL

The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries

(2011) Erich A. Nigg et al.   NATURE CELL BIOLOGY

Centrosomes and cilia in human disease

(2011) Mónica Bettencourt-Dias et al.   TRENDS IN GENETICS

Dual pathway spindle assembly increases both the speed and the fidelity of mitosis

(2011) K. Kaseda et al.   Biology Open

Novel CENPJ mutation causes Seckel syndrome

(2010) M. S. Al-Dosari et al.   JOURNAL OF MEDICAL GENETICS

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

(2010) Ersan Kalay et al.   NATURE GENETICS

The primary cilium: a signalling centre during vertebrate development

(2010) Sarah C. Goetz et al.   NATURE REVIEWS GENETICS

Centrioles, Centrosomes, and Cilia in Health and Disease

(2009) Erich A. Nigg et al.   CELL

Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families

(2009) M. Willems et al.   JOURNAL OF MEDICAL GENETICS

The Genome Response to Artificial Selection: A Case Study in Dairy Cattle

(2009) Laurence Flori et al.   PLoS One

Primary microcephaly: do all roads lead to Rome?

(2009) Gemma K. Thornton et al.   TRENDS IN GENETICS

A Generalized Caprine-like Hypoplasia Syndrome is localized within a 6-cM interval on bovine chromosome 13 in the Montbéliarde breed

(2008) A. Duchesne et al.   ANIMAL GENETICS

A novel function of CEP135 as a platform protein of C-NAP1 for its centriolar localization

(2008) Kyeongmi Kim et al.   EXPERIMENTAL CELL RESEARCH

In migrating cells, the Golgi complex and the position of the centrosome depend on geometrical constraints of the substratum

(2008) F. Pouthas et al.   JOURNAL OF CELL SCIENCE

Highly effective SNP-based association mapping and management of recessive defects in livestock

(2008) Carole Charlier et al.   NATURE GENETICS

Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

(2008) A. Rauch et al.   SCIENCE