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Items: 1 to 50 of 64

1.

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

Atkins M, Gasmi L, Bercier V, Revenu C, Del Bene F, Hazan J, Fassier C.

J Cell Biol. 2019 Oct 7;218(10):3290-3306. doi: 10.1083/jcb.201805128. Epub 2019 Sep 19.

PMID:
31541015
2.

Surgical Fixation of Metacarpal Shaft Fractures Using Absorbable Implants: A Systematic Review of the Literature.

Hazan J, Azzi AJ, Thibaudeau S.

Hand (N Y). 2019 Jan;14(1):19-26. doi: 10.1177/1558944718798856. Epub 2018 Sep 21.

PMID:
30239220
3.

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

Jardin N, Giudicelli F, Ten Martín D, Vitrac A, De Gois S, Allison R, Houart C, Reid E, Hazan J, Fassier C.

Development. 2018 Sep 12;145(17). pii: dev162701. doi: 10.1242/dev.162701.

4.

Scaphoid Cysts: Literature Review of Etiology, Treatment, and Prognosis.

Safran T, Hazan J, Al-Halabi B, Al-Naeem H, Cugno S.

Hand (N Y). 2018 Apr 1:1558944718769386. doi: 10.1177/1558944718769386. [Epub ahead of print]

PMID:
29661070
5.

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

Fassier C, Fréal A, Gasmi L, Delphin C, Ten Martin D, De Gois S, Tambalo M, Bosc C, Mailly P, Revenu C, Peris L, Bolte S, Schneider-Maunoury S, Houart C, Nothias F, Larcher JC, Andrieux A, Hazan J.

J Cell Biol. 2018 May 7;217(5):1719-1738. doi: 10.1083/jcb.201604108. Epub 2018 Mar 13.

6.

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

Fréal A, Fassier C, Le Bras B, Bullier E, De Gois S, Hazan J, Hoogenraad CC, Couraud F.

J Neurosci. 2016 Apr 20;36(16):4421-33. doi: 10.1523/JNEUROSCI.3219-15.2016.

7.

"There are many reasons why nurses avoid incident reporting".

Hazan J.

Nurs Times. 2015 Sep 23-29;111(39):7. No abstract available.

PMID:
26548277
8.

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

Pilorge M, Fassier C, Le Corronc H, Potey A, Bai J, De Gois S, Delaby E, Assouline B, Guinchat V, Devillard F, Delorme R, Nygren G, Råstam M, Meier JC, Otani S, Cheval H, James VM, Topf M, Dear TN, Gillberg C, Leboyer M, Giros B, Gautron S, Hazan J, Harvey RJ, Legendre P, Betancur C.

Mol Psychiatry. 2016 Jul;21(7):936-45. doi: 10.1038/mp.2015.139. Epub 2015 Sep 15.

9.

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

Allison R, Lumb JH, Fassier C, Connell JW, Ten Martin D, Seaman MN, Hazan J, Reid E.

J Cell Biol. 2013 Aug 5;202(3):527-43. doi: 10.1083/jcb.201211045. Epub 2013 Jul 29.

10.

Self-management for people with long-term neurological conditions.

Chaplin H, Hazan J, Wilson P.

Br J Community Nurs. 2012 Jun;17(6):250-4, 256-7.

PMID:
22875160
11.

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

Fassier C, Tarrade A, Peris L, Courageot S, Mailly P, Dalard C, Delga S, Roblot N, Lefèvre J, Job D, Hazan J, Curmi PA, Melki J.

Dis Model Mech. 2013 Jan;6(1):72-83. doi: 10.1242/dmm.008946. Epub 2012 Jul 5.

12.

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

Fassier C, Hutt JA, Scholpp S, Lumsden A, Giros B, Nothias F, Schneider-Maunoury S, Houart C, Hazan J.

Nat Neurosci. 2010 Nov;13(11):1380-7. doi: 10.1038/nn.2662. Epub 2010 Oct 10.

PMID:
20935645
13.

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

Stevanin G, Paternotte C, Coutinho P, Klebe S, Elleuch N, Loureiro JL, Denis E, Cruz VT, Dürr A, Prud'homme JF, Weissenbach J, Brice A, Hazan J.

Neurology. 2007 May 22;68(21):1837-40.

PMID:
17515546
14.

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

Klebe S, Durr A, Bouslam N, Grid D, Paternotte C, Depienne C, Hanein S, Bouhouche A, Elleuch N, Azzedine H, Poea-Guyon S, Forlani S, Denis E, Charon C, Hazan J, Brice A, Stevanin G.

Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):854-61.

PMID:
17503452
15.

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

McCormick LJ, Hutt JA, Hazan J, Houart C, Cohen J.

Gene Expr Patterns. 2007 Jan;7(3):289-96. Epub 2006 Sep 9.

PMID:
17045851
16.

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

Granata A, Savery D, Hazan J, Cheung BM, Lumsden A, Quaderi NA.

Dev Biol. 2005 Jan 15;277(2):417-24.

17.

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

Abel A, Fonknechten N, Hofer A, Dürr A, Cruaud C, Voit T, Weissenbach J, Brice A, Klimpe S, Auburger G, Hazan J.

Neurogenetics. 2004 Dec;5(4):239-43. Epub 2004 Oct 28.

PMID:
15517445
18.

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

Bönsch D, Schwindt A, Navratil P, Palm D, Neumann C, Klimpe S, Schickel J, Hazan J, Weiller C, Deufel T, Liepert J.

J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1109-12.

19.

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

Charvin D, Cifuentes-Diaz C, Fonknechten N, Joshi V, Hazan J, Melki J, Betuing S.

Hum Mol Genet. 2003 Jan 1;12(1):71-8.

PMID:
12490534
20.

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

Starling A, Rocco P, Passos-Bueno MR, Hazan J, Marie SK, Zatz M.

J Med Genet. 2002 Dec;39(12):e77. No abstract available.

21.

Hereditary spastic paraplegia caused by mutations in the SPG4 gene.

Bürger J, Fonknechten N, Hoeltzenbein M, Neumann L, Bratanoff E, Hazan J, Reis A.

Eur J Hum Genet. 2000 Oct;8(10):771-6.

22.

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

Lindsey JC, Lusher ME, McDermott CJ, White KD, Reid E, Rubinsztein DC, Bashir R, Hazan J, Shaw PJ, Bushby KM.

J Med Genet. 2000 Oct;37(10):759-65.

23.

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

Fontaine B, Davoine CS, Dürr A, Paternotte C, Feki I, Weissenbach J, Hazan J, Brice A.

Am J Hum Genet. 2000 Feb;66(2):702-7.

24.

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

Fonknechten N, Mavel D, Byrne P, Davoine CS, Cruaud C, Bönsch D, Samson D, Coutinho P, Hutchinson M, McMonagle P, Burgunder JM, Tartaglione A, Heinzlef O, Feki I, Deufel T, Parfrey N, Brice A, Fontaine B, Prud'homme JF, Weissenbach J, Dürr A, Hazan J.

Hum Mol Genet. 2000 Mar 1;9(4):637-44. Erratum in: Hum Mol Genet. 2005 Feb 1;14(3):461. Boentsch, D [corrected to Bönsch, D].

PMID:
10699187
25.

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

Zander C, Yuan QP, Lindblad K, Stevanin G, Dürr A, Davoine CS, Hazan J, Fontaine B, Brice A, Schalling M.

Neurosci Lett. 2000 Jan 21;279(1):41-4.

PMID:
10670783
26.

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

Hazan J, Fonknechten N, Mavel D, Paternotte C, Samson D, Artiguenave F, Davoine CS, Cruaud C, Dürr A, Wincker P, Brottier P, Cattolico L, Barbe V, Burgunder JM, Prud'homme JF, Brice A, Fontaine B, Heilig B, Weissenbach J.

Nat Genet. 1999 Nov;23(3):296-303.

PMID:
10610178
27.

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

Hazan J, Davoine CS, Mavel D, Fonknechten N, Paternotte C, Fizames C, Cruaud C, Samson D, Muselet D, Vega-Czarny N, Brice A, Gyapay G, Heilig R, Fontaine B, Weissenbach J.

Genomics. 1999 Sep 15;60(3):309-19.

PMID:
10493830
28.

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

Coutinho P, Barros J, Zemmouri R, Guimarães J, Alves C, Chorão R, Lourenço E, Ribeiro P, Loureiro JL, Santos JV, Hamri A, Paternotte C, Hazan J, Silva MC, Prud'homme JF, Grid D.

Arch Neurol. 1999 Aug;56(8):943-9.

PMID:
10448799
29.

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

Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, Weissenbach J, Hazan J.

Genome Res. 1998 Nov;8(11):1216-27.

30.

[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis].

von Fellenberg J, Paternotte C, Prud'homme JF, Weissenbach J, Hazan J, Burgunder JM.

Schweiz Med Wochenschr. 1998 Jun 27;128(26):1043-50. German.

PMID:
9700778
31.

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

Heinzlef O, Paternotte C, Mahieux F, Prud'homme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J.

J Med Genet. 1998 Feb;35(2):89-93.

32.

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B.

Brain. 1996 Oct;119 ( Pt 5):1487-96.

PMID:
8931574
33.

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

Vicart P, Dupret JM, Hazan J, Li Z, Gyapay G, Krishnamoorthy R, Weissenbach J, Fardeau M, Paulin D.

Hum Genet. 1996 Oct;98(4):422-9.

PMID:
8792816
34.

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

Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A.

Hum Genet. 1996 Sep;98(3):371-5.

PMID:
8707310
35.

A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J.

Nature. 1996 Mar 14;380(6570):152-4.

PMID:
8600387
36.

Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.

De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C.

Eur J Hum Genet. 1996;4(5):260-6.

PMID:
8946171
37.

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

Vincent P, Plauchu H, Hazan J, Fauré S, Weissenbach J, Godet J.

Hum Mol Genet. 1995 May;4(5):945-9. Erratum in: Hum Mol Genet 1995 Jul;4(7):1243.

PMID:
7633456
38.

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

Fontaine B, Rime CS, Hazan J, Dürr A, Stevanin G, Penet C, Reboul J, Agid Y, Lyon-Caen O, Baumann N, et al.

Neuromuscul Disord. 1995 Jan;5(1):11-7.

PMID:
7719135
39.

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

Deleuze JF, Dhorne S, Hazan J, Borghi E, Raynaud N, Pollet N, Meunier-Rotival M, Deschatrette J, Alagille D, Hadchouel M.

Mamm Genome. 1994 Nov;5(11):663-9.

PMID:
7873876
40.

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

James MR, Richard CW 3rd, Schott JJ, Yousry C, Clark K, Bell J, Terwilliger JD, Hazan J, Dubay C, Vignal A, et al.

Nat Genet. 1994 Sep;8(1):70-6.

PMID:
7987395
41.

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

Hazan J, Fontaine B, Bruyn RP, Lamy C, van Deutekom JC, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y, et al.

Hum Mol Genet. 1994 Sep;3(9):1569-73.

PMID:
7833913
42.

Genetic mapping of the human growth hormone-releasing factor gene (GHRF) using two intragenic polymorphisms detected by PCR amplification.

Pérez Jurado LA, Phillips JA 3rd, Summar ML, Mao J, Weber JL, Schaefer FV, Hazan J, Argente J.

Genomics. 1994 Mar 1;20(1):132-4.

PMID:
8020943
43.

The EUROGEM map of human chromosome 20.

Wunderle V, Dib C, Fizames C, Morisette J, Hazan J, Hansmann I, Whitehouse D, Vergnaud G, Weissenbach J.

Eur J Hum Genet. 1994;2(3):242-3. No abstract available.

PMID:
7834300
44.

Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients.

Deleuze JF, Hazan J, Dhorne S, Weissenbach J, Hadchouel M.

Eur J Hum Genet. 1994;2(3):185-90.

PMID:
7834278
45.

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

Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J.

Nat Genet. 1993 Oct;5(2):163-7.

PMID:
8252041
46.

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

Hazan J, Dubay C, Pankowiak MP, Becuwe N, Weissenbach J.

Genomics. 1992 Feb;12(2):183-9.

PMID:
1740328
47.

Energy expenditure during synthetic surfactant replacement therapy for neonatal respiratory distress syndrome.

Hazan J, Chessex P, Piedboeuf B, Bourgeois M, Bard H, Long W.

J Pediatr. 1992 Feb;120(2 Pt 2):S29-33.

PMID:
1735848
48.

A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3).

Bouloux PM, Hardelin JP, Munroe P, Kirk JM, Legouis R, Levilliers J, Hazan J, Weissenbach J, Petit C.

Nucleic Acids Res. 1991 Oct 11;19(19):5453. No abstract available.

49.

Association between hypothermia and mortality rate of premature infants--revisited.

Hazan J, Maag U, Chessex P.

Am J Obstet Gynecol. 1991 Jan;164(1 Pt 1):111-2.

PMID:
1986597
50.

Total parenteral nutrition in the newborn infant: energy substrates and respiratory gas exchange.

Piedboeuf B, Chessex P, Hazan J, Pineault M, Lavoie JC.

J Pediatr. 1991 Jan;118(1):97-102.

PMID:
1898751

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