Vincent A - Search Results

1

TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.

Ivanova EL, Gilet JG, Sulimenko V, Duchon A, Rudolf G, Runge K, Collins SC, Asselin L, Broix L, Drouot N, Tilly P, Nusbaum P, Vincent A, Magnant W, Skory V, Birling MC, Pavlovic G, Godin JD, Yalcin B, Hérault Y, Dráber P, Chelly J, Hinckelmann MV. Ivanova EL, et al. Among authors: vincent a. Nat Commun. 2019 May 13;10(1):2129. doi: 10.1038/s41467-019-10081-8. Nat Commun. 2019. PMID: 31086189 Free PMC article.

2

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.

Sellier C, Buijsen RAM, He F, Natla S, Jung L, Tropel P, Gaucherot A, Jacobs H, Meziane H, Vincent A, Champy MF, Sorg T, Pavlovic G, Wattenhofer-Donze M, Birling MC, Oulad-Abdelghani M, Eberling P, Ruffenach F, Joint M, Anheim M, Martinez-Cerdeno V, Tassone F, Willemsen R, Hukema RK, Viville S, Martinat C, Todd PK, Charlet-Berguerand N. Sellier C, et al. Among authors: vincent a. Neuron. 2017 Jan 18;93(2):331-347. doi: 10.1016/j.neuron.2016.12.016. Epub 2017 Jan 5. Neuron. 2017. PMID: 28065649 Free PMC article.

3

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.

Vincent A, Heitz D, Petit C, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Nature. 1991 Feb 14;349(6310):624-6. doi: 10.1038/349624a0. Nature. 1991. PMID: 1672039

4

New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.

Oberlé I, Vincent A, Abbadi N, Rousseau F, Hupkes PE, Hors-Cayla MC, Gilgenkrantz S, Oostra BA, Mandel JL. Oberlé I, et al. Among authors: vincent a. Am J Med Genet. 1991 Feb-Mar;38(2-3):336-42. doi: 10.1002/ajmg.1320380234. Am J Med Genet. 1991. PMID: 1673307

5

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Vincent A, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Hum Genet. 1989 Apr;82(1):85-6. doi: 10.1007/BF00288280. Hum Genet. 1989. PMID: 2565870

6

Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.

Sefiani A, M'rad R, Simard L, Vincent A, Julier C, Holvoet-Vermaut L, Heuertz S, Dahl N, Stalder JF, Peter MO, et al. Sefiani A, et al. Among authors: vincent a. Hum Genet. 1991 Jan;86(3):297-9. doi: 10.1007/BF00202414. Hum Genet. 1991. PMID: 1847690

7

Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis.

Fujita R, Hanauer A, Vincent A, Mandel JL, Koenig M. Fujita R, et al. Among authors: vincent a. Genomics. 1991 Aug;10(4):915-20. doi: 10.1016/0888-7543(91)90179-i. Genomics. 1991. PMID: 1916823

8

Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region.

Arveiler B, Vincent A, Mandel JL. Arveiler B, et al. Among authors: vincent a. Genomics. 1989 May;4(4):460-71. doi: 10.1016/0888-7543(89)90269-3. Genomics. 1989. PMID: 2501212

9

The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.

Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U. Vincent A, et al. Genomics. 1989 Nov;5(4):797-801. doi: 10.1016/0888-7543(89)90121-3. Genomics. 1989. PMID: 2574147

10

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).

Rousseau F, Vincent A, Rivella S, Heitz D, Triboli C, Maestrini E, Warren ST, Suthers GK, Goodfellow P, Mandel JL, et al. Rousseau F, et al. Among authors: vincent a. Am J Hum Genet. 1991 Jan;48(1):108-16. Am J Hum Genet. 1991. PMID: 1670748 Free PMC article.

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