Laurette Morlé: search on Z-Library

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1

16-P006 The ciliogenic transcription factor RFX3 is required for lung development in mice

Sébastien Sagnol, Laurette Morlé, Aouatef Ait-Lounis, Walter Reith, Bénédicte Durand

Journal:

Mechanisms of Development

Year:

2009

Language:

english

File:

PDF, 49 KB

english, 2009

2

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis

Akio Kanzaki, Sandrine Hayette, Laurette Morlé, Fumihide Inoue, Reiko Matsuyama, Takafumi Inoue, Ayumi Yawata, Hideho Wada, Agnes Vallier, Nicole Alloisio, Yoshihito Yawata, Jean Delaunay

Journal:

British Journal of Haematology

Year:

1997

Language:

english

File:

PDF, 646 KB

english, 1997

3

The red cell skeleton and its genetic disorders

Jean Delaunay, Nicole Alloisio, Laurette Morlé, Brigitte Pothier

Journal:

Molecular Aspects of Medicine

Year:

1990

Language:

english

File:

PDF, 5.91 MB

english, 1990

4

Alterations of Globin Chain Synthesis and of Red Cell Membrane Proteins in Congenital Dyserythropoietic Anemia I and II

Alloisio, Nicole, Jaccoud, Paule, Dorleac, Evelyne, Morle, Laurette, Philippe, Noel, Margueritte, Genevieve, Bryon, Paul A, Delaunay, Jean

Journal:

Pediatric Research

Year:

1982

Language:

english

File:

PDF, 565 KB

english, 1982

5

Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia

Laurette Morlé, Brigitte Pothier, Nicole Alloisio, Marie-Thérése Ducluzeau, Sandra Marques, Gabriel Olim, João Martins e Silva, Claude Féo, Michel Garbarz, Isabelle Chaveroche, Pierre Boivin, Jean Del

Journal:

European Journal of Haematology

Year:

1987

Language:

english

File:

PDF, 786 KB

english, 1987

6

RFX2 Is a Major Transcriptional Regulator of Spermiogenesis

Kistler, W. Stephen, Baas, Dominique, Lemeille, Sylvain, Paschaki, Marie, Seguin-Estevez, Queralt, Barras, Emmanuèle, Ma, Wenli, Duteyrat, Jean-Luc, Morlé, Laurette, Durand, Bénédicte, Reith, Walter,

Journal:

Year:

2015

Language:

english

File:

PDF, 11.53 MB

english, 2015

7

Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24

Lucie Verot, Nicole Alloisio, Laurette Morlé, Muriel Bozon, Renaud Touraine, Henri Plauchu, Patrick Edery

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 122 KB

english, 2003

8

The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab

François Morlé, Laurette Morlé, Faouzi Baklouti, Evelyne Dorléac, Claire Baudonnet, Jean Delaunay, Jacqueline Godet

Journal:

European Journal of Haematology

Year:

1984

Language:

english

File:

PDF, 448 KB

english, 1984

9

High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis

Emanuele Miraglia del Giudice, Matteo Francese, Bruno Nobili, Laurette Morlé, Stefano Cutillo, Jean Delaunay, Silverio Perrotta

Journal:

The Journal of Pediatrics

Year:

1998

Language:

english

File:

PDF, 274 KB

english, 1998

10

The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development

Benadiba, Carine, Magnani, Dario, Niquille, Mathieu, Morlé, Laurette, Valloton, Delphine, Nawabi, Homaira, Ait-Lounis, Aouatef, Otsmane, Belkacem, Reith, Walter, Theil, Thomas, Hornung, Jean-Pierre, L

Journal:

Year:

2012

Language:

english

File:

PDF, 5.50 MB

english, 2012

11

Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome 15q12–q15 and refinement to a 4.4 Mb region

Michon, Laetitia, Morlé, Laurette, Bozon, Muriel, Duret, Laurent, Zech, Jean-Christophe, Godet, Jacqueline, Plauchu, Henry, Edery, Patrick

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 144 KB

english, 2004

12

A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease mice

Karam, Alice, Tebbe, Lars, Weber, Chantal, Messaddeq, Nadia, Morlé, Laurette, Kessler, Pascal, Wolfrum, Uwe, Trottier, Yvon

Journal:

Neurobiology of Disease

Year:

2015

Language:

english

File:

PDF, 5.68 MB

english, 2015

13

Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss

Alloisio, Nicole, Morlé, Laurette, Bozon, Muriel, Godet, Jacqueline, Verhoeven, Kristien, Van Camp, Guy, Plauchu, Henri, Muller, Philippe, Collet, Lionel, Lina-Granade, Geneviève

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 116 KB

english, 1999

14

Transcriptional control of genes involved in ciliogenesis: a first step in making cilia

Joëlle Thomas, Laurette Morlé, Fabien Soulavie, Anne Laurençon, Sébastien Sagnol, Bénédicte Durand

Journal:

Biology of the Cell

Year:

2010

Language:

english

File:

PDF, 610 KB

english, 2010

15

Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14

Jean-Christophe Zech, Laurette Morlé, Pascale Vincent, Nicole Alloisio, Muriel Bozon, Colette Gonnet, Solange Milazzo, Jean-Daniel Grange, Christiane Trepsat, Jacqueline Godet, Henri Plauchu

Journal:

Graefe's Archive for Clinical and Experimental Ophthalmology

Year:

1999

Language:

english

File:

PDF, 307 KB

english, 1999

16

Altered GLI3 and FGF8 signaling underlies Acrocallosal syndrome phenotypes in Kif7 depleted mice

Putoux, Audrey, Baas, Dominique, Paschaki, Marie, Morlé, Laurette, Maire, Charline, Attié-Bitach, Tania, Thomas, Sophie, Durand, Bénédicte

Journal:

Human Molecular Genetics

Year:

2018

Language:

english

File:

PDF, 4.85 MB

english, 2018

17

Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome

Kloeckener-Gruissem, Barbara, Neidhardt, John, Magyar, István, Plauchu, Henri, Zech, Jean-Christophe, Morlé, Laurette, Palmer-Smith, Sheila M, MacDonald, Moira J, Nas, Véronique, Fry, Andrew E, Berger

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 844 KB

english, 2013

18

Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis

Philippe Maillet, Nicole Alloisio, Laurette Morlé, Jean Delaunay

Journal:

Year:

1996

Language:

english

File:

PDF, 1006 KB

english, 1996

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