Paternotte C[Author] - Search Results

Year	Number of Results
1951	1
1995	1
1996	2
1998	3
1999	4
2000	1
2001	3
2002	1
2003	2
2005	1
2007	2
2012	1
2013	1
2018	1
2019	1
2020	1
2024	0

1

Group adaptation, formal darwinism and contextual analysis.

Okasha S, Paternotte C. Okasha S, et al. Among authors: paternotte c. J Evol Biol. 2012 Jun;25(6):1127-39. doi: 10.1111/j.1420-9101.2012.02501.x. Epub 2012 Apr 5. J Evol Biol. 2012. PMID: 22487485 Free article.

2

Social evolution and the individual-as-maximising-agent analogy.

Paternotte C. Paternotte C. Stud Hist Philos Biol Biomed Sci. 2020 Feb;79:101225. doi: 10.1016/j.shpsc.2019.101225. Epub 2019 Nov 2. Stud Hist Philos Biol Biomed Sci. 2020. PMID: 31690488 Free article.

3

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. Dürr A, et al. Among authors: paternotte c. Brain. 1996 Oct;119 ( Pt 5):1487-96. doi: 10.1093/brain/119.5.1487. Brain. 1996. PMID: 8931574

4

Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.

Gücüyener K, Ozgül K, Paternotte C, Erdem H, Prud'homme JF, Ozgüç M, Topaloğlu H. Gücüyener K, et al. Among authors: paternotte c. Neuropediatrics. 2001 Jun;32(3):142-6. doi: 10.1055/s-2001-16616. Neuropediatrics. 2001. PMID: 11521210

5

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. Hazan J, et al. Among authors: paternotte c. Nat Genet. 1999 Nov;23(3):296-303. doi: 10.1038/15472. Nat Genet. 1999. PMID: 10610178

6

Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients.

Doudney K, Ybot-Gonzalez P, Paternotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P. Doudney K, et al. Among authors: paternotte c. Am J Med Genet A. 2005 Jul 1;136(1):90-2. doi: 10.1002/ajmg.a.30766. Am J Med Genet A. 2005. PMID: 15952208 No abstract available.

7

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. Coutinho P, et al. Among authors: paternotte c. Arch Neurol. 1999 Aug;56(8):943-9. doi: 10.1001/archneur.56.8.943. Arch Neurol. 1999. PMID: 10448799

8

Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.

Murdoch JN, Henderson DJ, Doudney K, Gaston-Massuet C, Phillips HM, Paternotte C, Arkell R, Stanier P, Copp AJ. Murdoch JN, et al. Among authors: paternotte c. Hum Mol Genet. 2003 Jan 15;12(2):87-98. doi: 10.1093/hmg/ddg014. Hum Mol Genet. 2003. PMID: 12499390

9

Genomic organization and embryonic expression of Igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia.

Murdoch JN, Doudney K, Gerrelli D, Wortham N, Paternotte C, Stanier P, Copp AJ. Murdoch JN, et al. Among authors: paternotte c. Mol Cell Neurosci. 2003 Jan;22(1):62-74. doi: 10.1016/s1044-7431(02)00021-0. Mol Cell Neurosci. 2003. PMID: 12595239

10

Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.

Doudney K, Murdoch JN, Braybrook C, Paternotte C, Bentley L, Copp AJ, Stanier P. Doudney K, et al. Among authors: paternotte c. Genomics. 2002 May;79(5):663-70. doi: 10.1006/geno.2002.6757. Genomics. 2002. PMID: 11991715

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