J. Hazan

发表

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Bertrand Fontaine, Patrick Wincker, Jean Weissenbach, 1999, Nature Genetics.

An ESCRT–spastin interaction promotes fission of recycling tubules from the endosome

J. Hazan, J. Connell, E. Reid, 2013, The Journal of cell biology.

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

J. Weissenbach, J. Hazan, H. Plauchu, 1995, Human molecular genetics.

Cooperative Interactions between 480 kDa Ankyrin-G and EB Proteins Assemble the Axon Initial Segment

C. Hoogenraad, Amélie Fréal, J. Hazan, 2016, The Journal of Neuroscience.

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description

S. Klebe, A. Durr, S. Hanein, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24

K. Lindblad, A. Brice, G. Stevanin, 2000, Neuroscience Letters.

Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice

P. Mailly, J. Melki, P. Curmi, 2012, Disease Models & Mechanisms.

BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation

J. Hazan, E. Reid, C. Fassier, 2018, Development.

Mouse Models of Autosomal Dominant Spastic Paraplegia

J. Melki, J. Hazan, C. Fassier, 2015 .

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

J. Weissenbach, A. Dürr, A. Brice, 2004, Neurogenetics.

Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus.

J. Melki, C. Cifuentes-Díaz, V. Joshi, 2003, Human molecular genetics.

Pure Familial Spastic Paraplegia: Clinical and Genetic Analysis of Nine Belgian Pedigrees

J. Weissenbach, C. Broeckhoven, J. Hazan, 1996, European journal of human genetics : EJHG.

Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree

M. Passos-Bueno, M. Zatz, J. Hazan, 2002, Journal of medical genetics.

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Y. Agid, J. Melki, A. Dürr, 1994, Human molecular genetics.

Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome.

J. Hazan, A. Lumsden, A. Granata, 2005, Developmental biology.

Mapping of Microsatellite Markers in the Alagille Region and Screening of Microdeletions by Genotyping 23 Patients

J. Weissenbach, J. Deleuze, J. Hazan, 1994, European journal of human genetics : EJHG.

Deleted Chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes

J. Deleuze, J. Deschatrette, J. Hazan, 1994, Mammalian Genome.

Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

R. Delorme, C. Gillberg, M. Leboyer, 2016, Molecular Psychiatry.

Hereditary spastic paraplegia caused by mutations in the SPG4 gene

A. Reis, J. Hazan, N. Fonknechten, 2000, European Journal of Human Genetics.

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

J. Weissenbach, J. Burgunder, J. Prud'homme, 2000, Human molecular genetics.

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.

J. Weissenbach, C. Dubay, J. Hazan, 1992, Genomics.

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

G. Gyapay, N. Drouot, C. Fizames, 1998, Genome research.

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

G. Gyapay, C. Fizames, D. Muselet, 1999, Genomics.

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

J. Weissenbach, J. Prud'homme, J. Pouget, 1998, Journal of medical genetics.

Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway

B. Giros, S. Scholpp, S. Schneider-Maunoury, 2010, Nature Neuroscience.

FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation

F. Del Bene, L. Gasmi, J. Hazan, 2019, The Journal of cell biology.

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

K. D. White, D. Rubinsztein, P. Shaw, 2000, Journal of medical genetics.

Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy

G. Gyapay, J. Weissenbach, J. Hazan, 1996, Human Genetics.

Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.

J. Prud'homme, J. Hazan, C. Paternotte, 1999, Archives of neurology.

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

J. Weissenbach, J. Burgunder, J. Prud'homme, 1996, Brain : a journal of neurology.

Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene

J. Liepert, C. Weiller, J. Hazan, 2003, Journal of neurology, neurosurgery, and psychiatry.

A key role for p60-Katanin in axon navigation is conditioned by the tubulin polyglutamylase TTLL6

C. Janke, L. Gasmi, J. Hazan, 2022, bioRxiv.

Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics

P. Mailly, S. Schneider-Maunoury, C. Delphin, 2018, The Journal of cell biology.

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

J. Weissenbach, A. Durr, A. Dürr, 2000, American journal of human genetics.

Mappingofacomplicated familial spastic paraplegia tolocus SPG4onchromosome 2p

J. Hazan, C. Paternotte, E. Roullet, 1998 .

The homeodomain transcription factor drg11 is expressed in primary sensory neurons and their putative CNS targets during embryonic development of the zebrafish.

J. Hazan, C. Houart, James Cohen, 2007, Gene expression patterns : GEP.

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

S. Klebe, C. Duyckaerts, C. van Broeckhoven, 2020, Genetics in Medicine.

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

S. Klebe, C. Duyckaerts, C. van Broeckhoven, 2020, Genetics in Medicine.

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

J. Weissenbach, A. Munnich, J. Melki, 1993, Nature genetics.

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

A. Reis, J. Hazan, C. Paternotte, 1996, Human Genetics.

In Vivo Live Imaging of Axonal Transport in Developing Zebrafish Axons.

J. Hazan, C. Fassier, Melody Atkins, 2022, Methods in molecular biology.

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21

J. Weissenbach, J. Prud'homme, A. Dürr, 2007, Neurology.

A key role for p60-Katanin in axon navigation is conditioned by the tubulin polyglutamylase TTLL6

J. Hazan, Nicolas Jardin, Coralie Fassier, 2022 .

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia

J. Weissenbach, Y. Agid, N. Baumann, 1995, Neuromuscular Disorders.