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51

Asymmetries of the conductance matrix in a three-terminal quantum ring in the Coulomb blockade regime

R. Leturcq, L. Schmid, T. Ihn, K. Ensslin, D.C. Driscoll, A.C. Gossard

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2006

Language:

english

File:

PDF, 145 KB

english, 2006

52

Probing the Kondo density of states in a three-terminal quantum ring

R. Leturcq, L. Schmid, K. Ensslin, Y. Meir, D.C. Driscoll, A.C. Gossard

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2006

Language:

english

File:

PDF, 174 KB

english, 2006

53

noise in a dilute GaAs two-dimensional hole system in the insulating phase

G. Deville, R. Leturcq, D. L’Hôte, R. Tourbot, C.J. Mellor, M. Henini

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2006

Language:

english

File:

PDF, 142 KB

english, 2006

54

Noise measurements in quantum dots using charge detection techniques

S. Gustavsson, R. Leturcq, T. Ihn, K. Ensslin, D.C. Driscoll, A.C. Gossard

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2007

Language:

english

File:

PDF, 337 KB

english, 2007

55

Aharonov–Bohm oscillations in p-type GaAs quantum rings

Boris Grbić, Renaud Leturcq, Thomas Ihn, Klaus Ensslin, Dirk Reuter, Andreas D. Wieck

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2008

Language:

english

File:

PDF, 520 KB

english, 2008

56

Pauli spin-blockade in an InAs nanowire double quantum dot

A. Pfund, I. Shorubalko, R. Leturcq, K. Ensslin

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2008

Language:

english

File:

PDF, 330 KB

english, 2008

57

Time-resolved interference experiments in a solid state environment

S. Gustavsson, R. Leturcq, M. Studer, T. Ihn, K. Ensslin, D.C. Driscoll, A.C. Gossard

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2008

Language:

english

File:

PDF, 354 KB

english, 2008

58

Strong spin–orbit interactions in carbon doped p-type GaAs heterostructures

B. Grbić, R. Leturcq, T. Ihn, K. Ensslin, D. Reuter, A.D. Wieck

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2008

Language:

english

File:

PDF, 147 KB

english, 2008

59

Frequency-selective single-photon detection with a double quantum dot

R. Leturcq, S. Gustavsson, M. Studer, T. Ihn, K. Ensslin, D.C. Driscoll, A.C. Gossard

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2008

Language:

english

File:

PDF, 535 KB

english, 2008

60

Time-resolved charge detection and back-action in quantum circuits

T. Ihn, S. Gustavsson, U. Gasser, R. Leturcq, I. Shorubalko, K. Ensslin

Journal:

Physica E: Low-dimensional Systems and Nanostructures

Year:

2010

Language:

english

File:

PDF, 418 KB

english, 2010

61

Quantum dots investigated with charge detection techniques

Thomas Ihn, Simon Gustavsson, Urszula Gasser, Bruno Küng, Thomas Müller, Roland Schleser, Martin Sigrist, Ivan Shorubalko, Renaud Leturcq, Klaus Ensslin

Journal:

Solid State Communications

Year:

2009

Language:

english

File:

PDF, 2.37 MB

english, 2009

62

Kondo effect in a three-terminal quantum ring

R. Leturcq, L. Schmid, K. Ensslin, D. C. Driscoll, A. C. Gossard

Journal:

physica status solidi (b)

Year:

2006

Language:

english

File:

PDF, 2.52 MB

english, 2006

63

Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter

Frédérique Tihy, Nicolas Vogt, Dominique Recan, Bernard Malfoy, France Leturcq, Michelle Coquet, Françoise Serville, Daniel Fontan, Jean-Michel Guillard, Jean-Claude Kaplan, Bernard Dutrillaux, Nicole

Journal:

Year:

1994

Language:

english

File:

PDF, 1.06 MB

english, 1994

64

Screening of the CAPN3 gene in patients with possible LGMD2A

Martin Krahn, Rafaëlle Bernard, Christophe Pécheux, El Hadi Hammouda, Bruno Eymard, Adolfo Lopez de Munain, Anna Maria Cobo, Norma Romero, Andoni Urtizberea, France Leturcq, Nicolas Lévy, The Calpain

Journal:

Clinical Genetics

Year:

2006

Language:

english

File:

PDF, 287 KB

english, 2006

65

Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay

M Krahn, C Pécheux, F Chapon, C Béroud, V Drouin-Garraud, P Laforet, NB Romero, I Penisson-Besnier, R Bernard, JA Urtizberea, F Leturcq, N Lévy

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 600 KB

english, 2007

66

Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

M Krahn, M Goicoechea, F Hanisch, E Groen, M Bartoli, C Pécheux, F Garcia-Bragado, F Leturcq, P-Y Jeannet, JA Lobrinus, S Jacquemont, J Strober, JA Urtizberea, A Saenz, K Bushby, N Lévy, A Lopez de Mu

Journal:

Clinical Genetics

Year:

2011

Language:

english

File:

PDF, 501 KB

english, 2011

67

Immunization of hu-PBL–SCID mice and the rescue of human monoclonal Fab fragments through combinatorial libraries

Duchosal, Michel A., Eming, Sabine A., Fischer, Peter, Leturcq, Didier, Barbas, Carlos F., McConahey, Patricia J., Caothien, Roger H., Dixon, Frank J., Burton, Dennis R.

Journal:

Year:

1992

File:

PDF, 499 KB

1992

68

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Piccolo, F., Roberds, S.L., Jeanpierre, M., Leturcq, F., Azibi, K., Beldjord, C., Carrié, A., Récan, D., Chaouch, M., Reghis, A.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 387 KB

1995

69

Conditional statistics of electron transport in interacting nanoscale conductors

Sukhorukov, Eugene V., Jordan, Andrew N., Gustavsson, Simon, Leturcq, Renaud, Ihn, Thomas, Ensslin, Klaus

Journal:

Year:

2007

Language:

english

File:

PDF, 334 KB

english, 2007

70

Design of Q-band loop-gap resonators at frequencies of 34–36 GHz for single electron spin spectroscopy in semiconductor nanostructures

Simovic, B., Studerus, P., Gustavsson, S., Leturcq, R., Ensslin, K., Schuhmann, R., Forrer, J., Schweiger, A.

Journal:

Review of Scientific Instruments

Year:

2006

Language:

english

File:

PDF, 981 KB

english, 2006

71

Asymmetric Franck-Condon factors in suspended carbon nanotube quantum dots

Cavaliere, Fabio, Mariani, Eros, Leturcq, Renaud, Stampfer, Christoph, Sassetti, Maura

Journal:

Physical Review B

Year:

2010

Language:

english

File:

PDF, 234 KB

english, 2010

72

Hepatitis B virus core antigen (HBc Ag) accumulation in an HBV nonproducer clone of HepG2-transfected cells is associated with cytopathic effect

Philippe Roingeard, Jean-Loup Romet-Lemonne, Didier Leturcq, Alain Goudeau, Max Essex

Journal:

Year:

1990

Language:

english

File:

PDF, 2.27 MB

english, 1990

73

Will you civil union me? Taxation and civil unions in France

Journal:

Journal of Public Economics

Year:

2012

Language:

english

File:

PDF, 843 KB

english, 2012

74

Lipopolysaccharide binding protein and soluble CD14 receptor protein in amniotic fluid and cord blood in patients at term

Thomas Roos, Thomas R. Martin, John T. Ruzinski, Didier J. Leturcq, Sharon L. Hillier, Dorothy L. Patton, David A. Eschenbach

Journal:

American Journal of Obstetrics and Gynecology

Year:

1997

Language:

english

File:

PDF, 805 KB

english, 1997

75

Human adult tonsil xenotransplantation into SCID mice for studying human immune responses and B cell lymphomagenesis

Michel A. Duchosal, Marie-Thérèse Fuzzati-Armentero, Roberto Baccala, Andreas Layer, Rosana Gonzalez-Quintial, Didier Leturcq, Marlies Rüegg, Philippe Trouillet, Sandrine Mauray, Jean-Daniel Tissot, M

Journal:

Experimental Hematology

Year:

2000

Language:

english

File:

PDF, 2.77 MB

english, 2000

76

High-level behavior of power rectifiers: A quantitative analysis of the forward voltage drop

Munoz-Yague, A., Leturcq, P.

Journal:

IEEE Transactions on Electron Devices

Year:

1978

Language:

english

File:

PDF, 864 KB

english, 1978

77

A comparative study of methods of measuring carrier lifetime in p-i-n devices

Derdouri, M., Leturcq, P., Munoz-Yague, A.

Journal:

IEEE Transactions on Electron Devices

Year:

1980

Language:

english

File:

PDF, 512 KB

english, 1980

78

Prenatal diagnosis of recessive congenital methaemoglobinaemia type II: novel mutation in the NADH-cytochrome b5 reductase gene leading to stop codon read-through

Alena Leroux, France Leturcq, Nathalie Deburgrave, Marie-France Szajnert

Journal:

European Journal of Haematology

Year:

2005

Language:

english

File:

PDF, 261 KB

english, 2005

79

Absence of γ-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

Daniel Jung, France Leturcq, Yoshihide Sunada, Franck Duclos, Fernando M.S. Tomé, Carolyn Moomaw, Luciano Merlini, Kemal Azibi, Malika Chaouch, Clive Slaughter, Michel Fardeau, Jean-Claude Kaplan, Kev

Journal:

Year:

1996

Language:

english

File:

PDF, 832 KB

english, 1996

80

Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)

J.-C. Kaplan, F. Piccolo, K. Azibi, A. Carrié, F. Leturcq, C. de Toma, C. Beldjord, M. Chaouch, A. Sefiani, L. Merlini, T. Voit, C. Sewry, Y. Sunada, J.S. Beckmann, N. Rornero, F.M.S. Tomé, M. Fardeau

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 101 KB

english, 1996

81

Aqueous alteration of nearly pure Nd-doped zirconolite (Ca0.8Nd0.2ZrTi1.8Al0.2O7), a passivating layer control

G. Leturcq, P.J. McGlinn, C. Barbe, M.G. Blackford, K.S. Finnie

Journal:

Applied Geochemistry

Year:

2005

Language:

english

File:

PDF, 464 KB

english, 2005

82

P.P.1 02 Combined approaches to diagnosis of congenital muscular dystrophies with α-dystroglycan hypoglycosylation

C. Bouchet, H. Manya, A. Yanagisawa, S. Maugenre, S. Quijano-Roy, B. Estournet, L. Merlini, H. Topaloglu, N.B. Romero, F. Leturcq, N. Seta, T. Endo, P. Guicheney

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 49 KB

english, 2006

83

G.P.4.09 Looking for a third gene causing Emery-Dreifuss muscular dystrophy: Lessons and perspectives

L. Gueneau, R. Ben Yaou, L. Demay, S. Llense, N. Deburgrave, F. Leturcq, P. Richard, G. Bonne

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 59 KB

english, 2006

84

P.P.1 01 Congenital muscular dystrophy with mental retradation due to a homozygous protein-o-mannosyltransferase 2 (POMT2) mutation: A case report

P.Y.K. Van den Bergh, C. Bouchet, S. Maugenre, A. Yanagisawa, G. Cosnard, F. Leturcq, N. Deburgrave, N. Séta, P. Guicheney

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 49 KB

english, 2006

85

G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy

Y.H. Hu, F. Leturcq, D. Héron, D. Logéart, S. Llense, J. Chelly, D. Récan, N.B. Romero, P. Lafôret, B. Eymard

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 44 KB

english, 2006

86

P.P.6 05 CAPN3 mutations in patients with idiopathic eosinophilic myositis

M. Krahn, A. Lopez de Munain, N. Streichenberger, R. Bernard, C. Pécheux, H. Testard, J.L. Pena-Segura, N.R. Romero, S. Bouillot-Eimer, X. Ferrer, M. Goicoechea, F. Garcia-Bragado, F. Leturcq, J.A. Ur

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 44 KB

english, 2006

87

T.O. 2 Rescue of dystrophin in the GRMD dog by multi-exon skipping using engineered U7 snRNAs

A. Vulin, A. Goyenvalle, I. Barthélémy, F. Leturcq, J.C. Kaplan, J. Chelly, O. Danos, S. Blot, L. Garcia

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 60 KB

english, 2006

88

G.P.4.10 Functional evaluation of a putative mini-dysferlin identified in a patient with moderate Miyoshi myopathy phenotype

M. Krahn, N. Wein, K. Nguyen, C. Vial, S. Courrier, W. Lostal, M. Bartoli, V. Labelle, F. Leturcq, P. Cau, I. Richard, N. Levy

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 47 KB

english, 2007

89

G.P.4.01 Mutational spectrum of the DYSF gene based on a large cohort of dysferlin deficient patients

M. Krahn, R. Bernard, K. Nguyen, V. Labelle, G. Bassez, D. Figarella-Branger, J. Pouget, E. Di Salvo, E. Hammouda, C. Béroud, B. Eymard, J.A. Urtizberea, F. Leturcq, N. Lévy

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 51 KB

english, 2007

90

G.P.1.15 Clinical description and molecular analysis of a promising model of DMD, the LRMD dog

I. Barthélémy, J. Thibaud, N. Carelle, L. Tiret, A. Vulin, C. Drougard, L. Garcia, J. Kaplan, F. Leturcq, S. Blot

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 46 KB

english, 2007

91

G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?

M. Krahn, F. Hanisch, M. Goicoechea, E. Groen, C. Pécheux, F. Garcia-Bragado, R. Layzer, F. Leturcq, J. Strober, J.A. Urtizberea, A. Sáenz, K. Bushby, N. Lévy, A. Lopez de Munain

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 63 KB

english, 2007

92

G.P.8.12 Molecular characterization and clinical update on one of the earliest described families with severe childhood autosomal recessive muscular dystrophy (SCARMD)

M. Salih, J.A. Urtizberea, F. Leturcq, M. Mukhtar, L. Anderson, K. Bushby

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

93

G.P.9.10 Clinical development of the French UMD–DMD database

V. Humbertclaude, S. Tuffery-Giraud, R. Ben Yaou, D. Hamroun, P. Khau Van Kien, F. Leturcq, J. Chelly, M. Claustres, C. Béroud

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 63 KB

english, 2007

94

C.P.3.03 Novel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly

A. Yanagisawa, C. Bouchet, H. Manya, S. Quijano-Roy, P. van den Bergh, L. Viollet, J. Cuisset, F. Leturcq, N. Romero, M. Fardeau, N. Seta, T. Endo, P. Guicheney

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 50 KB

english, 2007

95

G.P.1.03 Important variability in clinical severity in a family with Col VI-related myopathy: Potential implication of digenism?

F. Chapon, C. Gartioux, C. Ledeuil, L. Demay, L. Brinas, D. Herlicoviez, S. Allouche, A. Ferreiro, F. Leturcq, P. Richard, V. Allamand, G. Bonne

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 48 KB

english, 2008

96

G.O.5 Partial functionality of a Mini-dysferlin molecule identified in a patient affected with moderately severe primary dysferlinopathy

M. Krahn, N. Wein, W. Lostal, N. Bourg-Alibert, K. Nguyen, S. Courrier, C. Vial, V. Labelle, D. De Petris, A. Borges, M.G. Mattei, C. Roudaut, K. Miyake, P. McNeil, P. Cau, F. Leturcq, M. Bartoli, N.

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 48 KB

english, 2008

97

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H

Mireille Cossée, Clotilde Lagier-Tourenne, Claire Seguela, Michel Mohr, France Leturcq, Hulya Gundesli, Jamel Chelly, Christine Tranchant, Michel Koenig, Jean-Louis Mandel

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 1.45 MB

english, 2009

98

G.P.6.09 Immunolabelling and FACS as new tools to explore dysferlinopathies

W.N. Wein, K.M. Krahn, C.S. Courrier, S.C.E. Salort-Campana, N.K. Nguyen, F.C. Fernandez, P.J. Pouget, F.C. Fossat, D.D. Depetris, L.F. Leturcq, L.N. Lévy

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 53 KB

english, 2009

99

Immunolabelling and flow cytometry as new tools to explore dysferlinopathies

N. Wein, M. Krahn, S. Courrier, M. Bartoli, E. Salort-Campana, K. Nguyen, C. Fernandez, J. Pouget, C. Fossat, D. Depetris, F. Leturcq, P. Cau, N. Levy

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 861 KB

english, 2010

100

P1.15 DNA micro-arrays for revisiting molecular pathology in neuromuscular disorders

M. Cossée, M. Bartoli, V. Allamand, C. Guittard, V. Delague, M. Krahn, C. Ledeuil, I. Marey, I. Nelson, P. Richard, P. Bourgeois, G. Bonne, F. Leturcq, T. Voit, C. Béroud, J. Chelly, N. Lévy

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 39 KB

english, 2010

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