M. Bozon

发表

Association of an HLA-DQ allele with clinical tuberculosis.

E. Yunis, J. Delgado, S. Thim, 1998, JAMA.

MHC class II alleles and haplotypes in patients with pemphigus vulgaris from India.

N. Mehra, A. Ahmed, E. Yunis, 1996, Tissue antigens.

Genetic specification of left–right asymmetry in the diaphragm muscles and their motor innervation

Donna M. Martin, B. Durand, L. Moons, 2017, eLife.

SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate

O. Thoumine, S. Tauszig-Delamasure, V. Castellani, 2020, eLife.

A Spatiotemporal Sequence of Sensitization to Slits and Semaphorins Orchestrates Commissural Axon Navigation.

O. Thoumine, S. Tauszig-Delamasure, V. Castellani, 2019, Cell reports.

Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio

S. Perrotta, A. Iolascon, J. Randon, 1997, British journal of haematology.

Error rate for HLA-B antigen assignment by serology: implications for proficiency testing and utilization of DNA-based typing methods.

J. Russell, B. Dupont, N. Yu, 1997, Tissue antigens.

Motoneuronal Sema3C is essential for setting stereotyped motor tract positioning in limb-derived chemotropic semaphorins

V. Castellani, Frédéric Moret, M. Bozon, 2012, Development.

Two distinct truncated variants of ankyrin associated with hereditary spherocytosis

S. Hayette, O. Reman, P. Maillet, 1998, American journal of hematology.

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

S. Hayette, B. Forget, J. Delaunay, 1997, American journal of hematology.

Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis

S. Perrotta, A. Iolascon, S. Hayette, 1996, British journal of haematology.

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia

M. Tanner, S. Hayette, C. M. Cohen, 1995, British journal of haematology.

X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variant

R. Touraine, B. Gérard, A. Piton, 2021, neurogenetics.

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis.

M. Tanner, P. Maillet, M. Ribeiro, 1997, Blood.

Iterative inhibition of commissural growth cone exploration, not post-crossing barrier, ensures forward midline navigation through SlitC-PlxnA1 signaling

O. Thoumine, S. Tauszig-Delamasure, V. Castellani, 2020, bioRxiv.

A balance of noncanonical Semaphorin signaling from the cerebrospinal fluid regulates apical cell dynamics during corticogenesis

D. Jabaudon, V. Castellani, M. Bozon, 2022, Science advances.

An unconventional cerebrospinal fluid-derived Semaphorin-signalling regulates apical progenitor dynamics in the developing neocortex

D. Jabaudon, V. Castellani, M. Bozon, 2020, bioRxiv.

New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia.

P. Denis, P. Edery, F. Béby, 2007, Archives of ophthalmology.

Microenvironment-Driven Shift of Cohesion/Detachment Balance within Tumors Induces a Switch toward Metastasis in Neuroblastoma.

S. Tauszig-Delamasure, V. Combaret, V. Castellani, 2017, Cancer cell.

A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

C. Philippe, J. Zech, J. Lambert, 2000, American journal of human genetics.

A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon

P. Maillet, J. Delaunay, F. Baklouti, 1999, Human mutation.

A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss

P. Latour, G. Lina-Granade, H. Plauchu, 2000, Journal of medical genetics.

X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variant

R. Touraine, B. Gérard, A. Piton, 2021, neurogenetics.

Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus

N. Drouot, T. Frebourg, V. Castellani, 2012, neurogenetics.

Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14

C. Gonnet, J. Zech, H. Plauchu, 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.

Comparison of HLA-A antigen typing by serology with two polymerase chain reaction based DNA typing methods: implications for proficiency testing.

B. Dupont, E. Yunis, J. Delgado, 1996, Tissue antigens.

Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis

A. Pierani, F. Causeret, V. Castellani, 2015, Nature Communications.

gdnf Activates Midline Repulsion by Semaphorin3B via NCAM during Commissural Axon Guidance

V. Castellani, K. Wright, F. Helmbacher, 2012, Neuron.

Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.

R. Touraine, V. Bernard, A. Calender, 2007, European journal of medical genetics.

Semaphorin and neuropilin co-expression in motoneurons sets axon sensitivity to environmental semaphorin sources during motor axon pathfinding

V. Castellani, M. Bozon, Frédéric Moret, 2007, Development.

Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss

L. Collet, K. Verhoeven, G. Lina-Granade, 1999, European Journal of Human Genetics.

A midline switch of receptor processing regulates commissural axon guidance in vertebrates.

Yutaka Yoshida, V. Castellani, A. Kumanogoh, 2010, Genes & development.

Spatial and temporal profiling of receptor membrane insertion controls commissural axon responses to midline repellents

O. Thoumine, S. Tauszig-Delamasure, V. Castellani, 2019, bioRxiv.

A Spatio-Temporal Sequence of Axonal Sensitization to Slits and Semaphorins Orchestrates Commissural Axon Navigation

O. Thoumine, S. Tauszig-Delamasure, V. Castellani, 2019, SSRN Electronic Journal.

Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus

N. Drouot, T. Frebourg, V. Castellani, 2012, neurogenetics.

Dual Functional Activity of Semaphorin 3B Is Required for Positioning the Anterior Commissure

J. Sanes, G. Rougon, A. Püschel, 2005, Neuron.

Dual Functional Activity of Semaphorin 3B Is Required for Positioning the Anterior Commissure

J. Sanes, G. Rougon, A. Püschel, 2005, Neuron.

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.

S. Hayette, J. Delaunay, D. Dhermy, 1995, Blood.

The dependence receptor TrkC regulates the number of sensory neurons during DRG development.

C. Costechareyre, J. Blachier, L. Jarrosson-Wuillème, 2018, Developmental biology.

FAK–MAPK‐dependent adhesion disassembly downstream of L1 contributes to semaphorin3A‐induced collapse

M. Tessier-Lavigne, A. Yaron, J. Guan, 2008, The EMBO journal.

Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24

R. Touraine, H. Plauchu, P. Edery, 2003, American journal of medical genetics. Part A.

Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis

A. Pierani, V. Castellani, J. Falk, 2015, Nature Communications.

Microenvironment-Driven Shift of Cohesion/Detachment Balance within Tumors Induces a Switch toward Metastasis in Neuroblastoma.

S. Tauszig-Delamasure, V. Combaret, V. Castellani, 2017, Cancer Cell.