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1

Corps GW et granules de stress, deux structures cytoplasmiques pour la dégradation et le stockage des ARNm dans les cellules de mammifère.

Weil, Dominique

Journal:

Journal de la Société de Biologie

Year:

2007

File:

PDF, 817 KB

2007

2

Linkage studies of enzyme markers in man-mouse somatic cell hybrids

CLAUDE BILLARDON, NGUYEN VAN CONG, JEAN-YVES PICARD, CHARLES LE BORGNE de KAOUËL, RÉGIS REBOURCET, DOMINIQUE WEIL, JOSUÉ FEINGOLD, JEAN FRÉZAL

Journal:

Annals of Human Genetics

Year:

1973

Language:

english

File:

PDF, 929 KB

english, 1973

3

Absence of Bacterial Imprints on Struvite-containing Kidney Stones: A Structural Investigation at the Mesoscopic and Atomic Scale

Dominique Bazin, Gilles André, Raphael Weil, Guy Matzen, Veron Emmanuel, Xavier Carpentier, M. Daudon

Journal:

Year:

2012

Language:

english

File:

PDF, 887 KB

english, 2012

4

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

Francoise Denoyelle, Sandrine Marlin, Dominique Weil, Lucien Moatti, Pierre Chauvin, Éréa-Noël Garabédian, Christine Petit

Journal:

Year:

1999

Language:

english

File:

PDF, 132 KB

english, 1999

5

The embalmed heart of Richard the Lionheart (1199 A.D.): a biological and anthropological analysis

Charlier, Philippe, Poupon, Joël, Jeannel, Gaël-François, Favier, Dominique, Popescu, Speranta-Maria, Weil, Raphaël, Moulherat, Christophe, Huynh-Charlier, Isabelle, Dorion-Peyronnet, Caroline, Lazar,

Journal:

Scientific Reports

Year:

2013

Language:

english

File:

PDF, 4.71 MB

english, 2013

6

Teratoma in an Undescended Testis Detected Prenatally

Mboyo, Antoine, Foulet, Armelle, Hocine, Samia, Cheve, Marie-Therese, Plat, Monique, Weil, Dominique

Journal:

The Journal of Urology

Year:

1997

Language:

english

File:

PDF, 705 KB

english, 1997

7

Management of gastric varices

Weil, Delphine, Cervoni, Jean-Paul, Fares, Nadim, Rudler, Marika, Bureau, Christophe, Plessier, Aurélie, Dao, Thong, Pauwels, Arnaud, Thabut, Dominique, Castellani, Paul, Oberti, Frederic, Carbonell,

Journal:

European Journal of Gastroenterology & Hepatology

Year:

2016

Language:

english

File:

PDF, 147 KB

english, 2016

8

Detection of silica and calcium carbonate deposits in granulomatous areas of skin sarcoidosis by μFourier transform infrared spectroscopy and Field Emission Scanning Electron Microscopy coupled with Energy Dispersive X-ray Spectroscopy analysis

Colboc, Hester, Bazin, Dominique, Moguelet, Philippe, Frochot, Vincent, Weil, Raphaël, Letavernier, Emmanuel, Jouanneau, Chantal, Francès, Camille, Bachmeyer, Claude, Bernaudin, Jean-François, Daudon,

Journal:

Comptes Rendus Chimie

Year:

2016

Language:

english

File:

PDF, 5.42 MB

english, 2016

9

Tau/DDX6 interaction increases microRNA activity

Chauderlier, Alban, Gilles, Melissa, Spolcova, Andrea, Caillierez, Raphaelle, Chwastyniak, Maggy, Kress, Michel, Drobecq, Herve, Bonnefoy, Eliette, Pinet, Florence, Weil, Dominique, Buée, Luc, Galas,

Journal:

Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms

Year:

2018

Language:

english

File:

PDF, 5.31 MB

english, 2018

10

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Elisabeth Verpy, Michel Leibovici, Nicolas Michalski, Richard J. Goodyear, Carine Houdon, Dominique Weil, Guy P. Richardson, Christine Petit

Journal:

The Journal of Comparative Neurology

Year:

2011

Language:

english

File:

PDF, 5.08 MB

english, 2011

11

Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells

Amel Bahloul, Marie-Christine Simmler, Vincent Michel, Michel Leibovici, Isabelle Perfettini, Isabelle Roux, Dominique Weil, Sylvie Nouaille, Jian Zuo, Cristina Zadro, Danilo Licastro, Paolo Gasparini

Journal:

EMBO Molecular Medicine

Year:

2009

Language:

english

File:

PDF, 1.50 MB

english, 2009

12

Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss

Abdelaziz Tlili, Ilhem Charfedine, Imed Lahmar, Zaineb Benzina, Ben Amor Mohamed, Dominique Weil, Nabil Idriss, Mohamed Drira, Saber Masmoudi, Hammadi Ayadi

Journal:

Year:

2005

Language:

english

File:

PDF, 65 KB

english, 2005

13

CDC2L5, a Cdk-like kinase with RS domain, interacts with the ASF/SF2-associated protein p32 and affects splicing in vivo

Yasmine Even, Sandrine Durieux, Marie-Line Escande, Jean Claude Lozano, Gérard Peaucellier, Dominique Weil, Anne-Marie Genevière

Journal:

Journal of Cellular Biochemistry

Year:

2006

Language:

english

File:

PDF, 396 KB

english, 2006

14

Screening mutations ofOTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy

Da-Yong Wang, Yi-Chen Wang, Dominique Weil, Ya-Li Zhao, Shao-Qi Rao, Liang Zong, Yu-Bin Ji, Qiong Liu, Jian-Qiang Li, Huan-Ming Yang, Yan Shen, Cindy Benedict-Alderfer, Qing-Yin Zheng, Christine Petit

Journal:

BMC Medical Genetics

Year:

2010

Language:

english

File:

PDF, 1.09 MB

english, 2010

15

Localisation du gene de l'α-glucosidase acide (α-GLUa) sur le segment q21→qter du chromosome 17 par l'hybridation cellulaire interspecifique

Dominique Weil, Nguyen Van Cong, Marie-Sylvie Gross, J. Frézal

Journal:

Year:

1979

Language:

english

File:

PDF, 717 KB

english, 1979

16

Localisation régionale des gènes humains IDHS, MDHS, PGK, α-GAL, G6PD par l'hybridation cellulaire interspécifique

Dominique Weil, Nguyen Van-Cong, Catherine Finaz, R. Rebourcet, Chantal Cochet, J. Grouchy, J. Frézal

Journal:

Year:

1977

Language:

english

File:

PDF, 300 KB

english, 1977

17

Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen

P. Tsipouras, P. H. Byers, R. C. Schwartz, Mon-Li Chu, Dominique Weil, Guglielmina Pepe, Suzanne B. Cassidy, F. Ramirez

Journal:

Year:

1986

Language:

english

File:

PDF, 579 KB

english, 1986

18

Localisation régionale des gènes humains LDHB, TPI, ENO2, PepB, PGK, αGALA, G6PD et HGPRT par l'hybridation cellulaire interspécifique

Dominique Weil, Nguyen Van-Cong, R. Rebourcet, J. Frézal

Journal:

Year:

1978

Language:

english

File:

PDF, 395 KB

english, 1978

19

Biochemical evidence for the non-inactivation of the steroid sulfatase locus in human placenta and fibroblasts

Monique Bedin, Dominique Weil, Thérèse Fournier, Lise Cedard, Jean Frezal

Journal:

Year:

1981

Language:

english

File:

PDF, 284 KB

english, 1981

20

Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay

H. Verneuil, B. Grandchamp, Chantal Foubert, Dominique Weil, Cong N'Guyen, Marie-Sylvie Gross, Shigeru Sassa, Y. Nordmann

Journal:

Year:

1984

Language:

english

File:

PDF, 304 KB

english, 1984

21

Localisation du gène phosphoglycolate phosphatase (PGP) sur le chromosome 16 par l'hybridation cellulaire interspecifique

Dominique Weil, Nguyen Van Cong, Catherine Finaz, Marie-Sylvie Gross, Chantal Cochet, J. Grouchy, J. Frézal

Journal:

Year:

1979

File:

PDF, 356 KB

1979

22

Assignment of NADH-cytochrome b5reductase (DIA1locus) to human chromosome 22

Claudine Junien, Magdeleine Vibert, Dominique Weil, Nguyen Van-Cong, Jean-Claude Kaplan

Journal:

Year:

1978

Language:

english

File:

PDF, 377 KB

english, 1978

23

The proα2 (V) collagen gene (COL5A2) maps to 2q14→2q32, syntenic to the proα1 (III) collagen locus (COL3A1)

Cécile Huerre-Jeanpierre, Isabelle Henry, M. Bernard, Pia Gallano, Dominique Weil, K. H. Grzeschik, F. Ramirez, Claudine Junien

Journal:

Year:

1986

Language:

english

File:

PDF, 374 KB

english, 1986

24

The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specific

M. Jeanpierre, Dominique Weil, Pia Gallano, Nicole Creau-Goldberg, Claudine Junien

Journal:

Year:

1985

Language:

english

File:

PDF, 877 KB

english, 1985

25

Assignment of the human coproporphyrinogen oxidase to chromosome 9

B. Grandchamp, Dominique Weil, Y. Nordmann, N. Cong, H. Verneuil, Chantal Foubert, Marie-Sylvie Gross

Journal:

Year:

1983

Language:

english

File:

PDF, 240 KB

english, 1983

26

cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31

Marie-Geneviève Mattei, Dominique Weil, Dorothy Pribula-Conway, Michael P. Bernard, Edith Passage, N'Guyen Van Cong, Rupert Timpl, Mon-Li Chu

Journal:

Year:

1988

Language:

english

File:

PDF, 630 KB

english, 1988

27

Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

Nicolas Michalski, Vincent Michel, Elisa Caberlotto, Gaelle M. Lefèvre, Alexander F. J. van Aken, Jean-Yves Tinevez, Emilie Bizard, Christophe Houbron, Dominique Weil, Jean-Pierre Hardelin, Guy P. Ric

Journal:

Pflügers Archiv European Journal of Physiology

Year:

2009

Language:

english

File:

PDF, 844 KB

english, 2009

28

A novel locus for Usher syndrome type

Mirna Mustapha, Éliane Chouery, Delphine Torchard-Pagnez, Sylvie Nouaille, Awni Khrais, Fouad N. Sayegh, André Mégarbané, Jacques Loiselet, Mark Lathrop, Christine Petit, Dominique Weil

Journal:

Year:

2002

Language:

english

File:

PDF, 41 KB

english, 2002

29

Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralin

Mireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, Jean-Michel Griffoin, Dominique Weil, Mariona Arbones, Robert Vincent, Christian P. Hamel

Journal:

Year:

2003

Language:

english

File:

PDF, 315 KB

english, 2003

30

Acremonium strictumFungaemia in a Paediatric Immunocompromised Patient: Diagnosis and Treatment Difficulties

Hikombo Hitoto, Marc Pihet, Béatrice Weil, Dominique Chabasse, Jean-Philippe Bouchara, Petronella Rachieru-Sourisseau

Journal:

Year:

2010

Language:

english

File:

PDF, 240 KB

english, 2010

31

10.1038/30639

Denoyelle, Françoise, Lina-Granade, Genevieve, Plauchu, Henri, Bruzzone, Roberto, Chaïb, Hassan, Lévi-Acobas, Fabienne, Weil, Dominique, Petit, Christine

Journal:

Year:

1998

Language:

english

File:

PDF, 202 KB

english, 1998

32

Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1

Masmoudi, Saber, Medlej-Hashim, Myrna, Chouery, Eliane, Weil, Dominique, Ayadi, Hammadi, Petit, Christine, Mégarbané, André, Belguith, Hanen

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 154 KB

english, 2008

33

Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

Verpy, Elisabeth, Weil, Dominique, Leibovici, Michel, Goodyear, Richard J., Hamard, Ghislaine, Houdon, Carine, Lefèvre, Gaelle M., Hardelin, Jean-Pierre, Richardson, Guy P., Avan, Paul

Journal:

Year:

2008

Language:

english

File:

PDF, 1.81 MB

english, 2008

34

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Abdelhak, Sonia, Kalatzis, Vasiliki, Heilig, Roland, Compain, Sylvie, Samson, Delphine, Vincent, Christophe, Weil, Dominique, Cruaud, Corinne, Sahly, Iman, Leibovici, Michel

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.55 MB

1997

35

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

Weil, Dominique, Küssel, Polonca, Blanchard, Stéphane, Lévy, Gallia, Levi-Acobas, Fabienne, Drira, Mohamed, Ayadi, Hammadi, Petit, Christine

Journal:

Nature Genetics

Year:

1997

File:

PDF, 361 KB

1997

36

Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness

Weil, Dominique, Wang, Irène, Dietrich, Alexander, Poustka, Annemarie, Weissenbach, Jean, Petit, Christine

Journal:

Nature Genetics

Year:

1994

File:

PDF, 702 KB

1994

37

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Mburu, Philomena, Mustapha, Mirna, Varela, Anabel, Weil, Dominique, El-Amraoui, Aziz, Holme, Ralph H, Rump, Andreas, Hardisty, Rachel E, Blanchard, Stéphane, Coimbra, Roney S

Journal:

Nature Genetics

Year:

2003

Language:

english

File:

PDF, 3.19 MB

english, 2003

38

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

Delmaghani, Sedigheh, del Castillo, Francisco J, Michel, Vincent, Leibovici, Michel, Aghaie, Asadollah, Ron, Uri, Van Laer, Lut, Ben-Tal, Nir, Van Camp, Guy, Weil, Dominique

Journal:

Nature Genetics

Year:

2006

Language:

english

File:

PDF, 638 KB

english, 2006

39

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness

Mustapha, Mirna, Salem, Nabiha, Weil, Dominique, El-Zir, Elie, Loiselet, Jacques, Petit, Christine

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 51 KB

english, 1999

40

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations

Medlej-Hashim, Myrna, Mustapha, Mirna, Chouery, Eliane, Weil, Dominique, Parronaud, Joel, Salem, Nabiha, Delague, Valérie, Loiselet, Jacques, Lathrop, Mark, Petit, Christine

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 92 KB

english, 2002

41

Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor

Chapiro, Elise, Feldmann, Delphine, Denoyelle, Françoise, Sternberg, Damien, Jardel, Claude, Eliot, Marie-Madeleine, Bouccara, Didier, Weil, Dominique, Garabédian, Eréa-Noel, Couderc, Rémy

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 159 KB

english, 2002

42

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

Masmoudi, Saber, Tlili, Abdelaziz, Majava, Marja, Ghorbel, Abdel Monem, Chardenoux, Sébastien, Lemainque, Arnaud, Zina, Zeineb Ben, Moala, Jihene, Männikkö, Minna, Weil, Dominique

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 90 KB

english, 2003

43

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21–12.1

Delmaghani, Sedigheh, Aghaie, Asadollah, Compain-Nouaille, Sylvie, Ataie, Afsaneh, Lemainque, Arnaud, Zeinali, Sirous, Lathrop, Mark, Weil, Dominique, Petit, Christine

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 75 KB

english, 2003

44

Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene

Feldmann, Delphine, Denoyelle, Françoise, Loundon, Natalie, Weil, Dominique, Garabedian, Erea-Noel, Couderc, Remy, Joannard, Alain, Schmerber, Sébastien, Delobel, Bruno, Leman, Jacques

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 161 KB

english, 2003

45

Regulation of pre-mRNA processing by src

Henry Neel, Pierre Gondran, Dominique Weil, François Dautry

Journal:

Current Biology

Year:

1995

Language:

english

File:

PDF, 3.00 MB

english, 1995

46

Assignment of the ǵene for F-type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitation

DOMINIQUE WEIL, DOMINIQUE COTTREAU, NGUYEN VAN CONG, RÉGIS REBOURCET, CHANTAL FOUBERT, MARIE-SYLVIE GROSS, JEAN-CLAUDE DREYFUS, AXEL KAHN

Journal:

Annals of Human Genetics

Year:

1980

Language:

english

File:

PDF, 374 KB

english, 1980

47

Preparation of Optical Quality ZnCdTe Thin Films by Vacuum Evaporation

Weil, Raoul, Joucla, Marguerite, Loison, Jean Luc, Mazilu, Michaël, Ohlmann, Dominique, Robino, Michèle, Schwalbach, Georges

Journal:

Year:

1998

Language:

english

File:

PDF, 460 KB

english, 1998

48

A YAC Contig and an EST Map in the Pericentromeric Region of Chromosome 13 Surrounding the Loci for Neurosensory Nonsyndromic Deafness (DFNB1 and DFNA3) and Limb-Girdle Muscular Dystrophy Type 2C (LGMD2C)

Parry Guilford, Catherine Dodé, Fabien Crozet, Stéphane Blanchard, Hassan Chaı̈b, Jacqueline Levilliers, Fabienne Levi-Acobas, Dominique Weil, Jean Weissenbach, Daniel Cohen, Denis Le Paslier, Jean-Cl

Journal:

Year:

1995

File:

PDF, 426 KB

1995

49

Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2)

Catherine Dodé, Dominique Weil, Jacqueline Levilliers, Fabien Crozet, Hassan Chaı&amp, #x0308, b, Fabienne Levi-Acobas, Parry Guilford, Christine Petit

Journal:

Year:

1998

Language:

english

File:

PDF, 302 KB

english, 1998

50

Monoarthritis induces complex changes in μ-, δ- and κ-opioid binding sites in the superficial dorsal horn of the rat spinal cord

Dominique Besse, Jeanne Weil-Fugazza, Marie-Christine Lombard, Stephen H. Butler, Jean-Marie Besson

Journal:

European Journal of Pharmacology

Year:

1992

Language:

english

File:

PDF, 1.37 MB

english, 1992

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