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Thrombin generation in patients with factor XI deficiency and clinical bleeding risk

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-09, Vol.16 (5), p.771-777

2010

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Proadipogenic effect of leptin on rat preadipocytes in vitro: activation of MAPK and STAT3 signaling pathways

American Journal of Physiology: Cell Physiology, 2002-04, Vol.282 (4), p.C853-C863

2002

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Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Journal of thrombosis and haemostasis, 2004-01, Vol.2 (1), p.71-76

2004

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Characterization of combined factor VII and factor XI deficiencies

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-05, Vol.14 (3), p.639-642

2008

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Expression studies of key adipogenic transcriptional factors reveal that the anti-adipogenic properties of retinol in primary cultured human preadipocytes are due to retinol per se

International journal of cosmetic science, 2001-10, Vol.23 (5), p.299-308

2001

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The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal A{alpha} disulfide bonds in protein assembly and secretion

Haematologica (Roma), 2011-08, Vol.96 (8), p.1226-1230

2011

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Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Journal of thrombosis and haemostasis, 2007-10, Vol.5 (10), p.1999-2005

2007

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Leptin mediates a proliferative response in human MCF7 breast cancer cells

Biochemical and biophysical research communications, 2002-04, Vol.293 (1), p.622-628

2002

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Direct in vitro effects of androgens and estrogens on ob gene expression and leptin secretion in human adipose tissue

Endocrine, 2002-07, Vol.18 (2), p.179-184

2002

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Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K)

Haematologica (Roma), 2005-08, Vol.90 (8), p.1149-1150

2005

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Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency

Blood coagulation & fibrinolysis, 2006-01, Vol.17 (1), p.69-73

2006

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Characterization of combined factor VII and factor XI deficiencies

Haemophilia : the official journal of the World Federation of Hemophilia, 2008, Vol.14 (3), p.639-642

2008

Volltextzugriff (PDF)

Proadipogenic effect of leptin on rat preadipocytes in vitro: activation of MAPK and STAT3 signaling pathways

American Journal of Physiology: Cell Physiology, 2002-04, Vol.51 (4), p.C853-C863

2002

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100 children treated by the combination of propionylerythromycin (in the form of the laurylsulfate) and trisulfazine. Granules suspended in a syrup

Gazette medicale de France, 1961-12, Vol.68, p.2987

1961

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Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients

Clinical genetics, 2018-03, Vol.93 (3), p.567-576

2018

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Significant decrease of the optical losses in the coupling between colloidal CdSe/CdS nanocrystals and a flat gold film at cryogenic temperature

Physical review. B, 2017-11, Vol.96 (19), Article 195416

2017

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Aide médicale à la procréation, malformations congénitales et santé postnatale

Revue de médecine périnatale, 2022-06, Vol.14 (2), p.77

2022

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Unraveling the time cross correlations of an emitter switching between two states with the same fluorescence intensity

Optics express, 2015-11, Vol.23 (23), p.29921-29928

2015

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Enhanced and polarized emission from single colloidal CdSe/CdS nanocrystals coupled to a one-dimensional gold grating

Physical review. B, 2016-08, Vol.94 (8), Article 085301

2016

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LHX2 haploinsufficiency causes a variable neurodevelopmental disorder

Genetics in medicine, 2023-07, Vol.25 (7), p.100839, Article 100839

2023

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Thermal activation of non-radiative Auger recombination in charged colloidal nanocrystals

Nature nanotechnology, 2013-03, Vol.8 (3), p.206-212

2013

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Fetal costello syndrome with neuromuscular spindle excess and p.Gly12Val HRAS mutation

European journal of medical genetics, 2017-07, Vol.60 (7), p.395-398

2017

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Clinical delineation of SETBP1 haploinsufficiency disorder

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1198-1205

2021

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IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Genetics in medicine, 2019-04, Vol.21 (4), p.837-849

2019

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Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

Clinical genetics, 2014-10, Vol.86 (4), p.326-334

2014

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Thrombin generation in patients with factor XI deficiency and clinical bleeding risk

Proadipogenic effect of leptin on rat preadipocytes in vitro: activation of MAPK and STAT3 signaling pathways

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Characterization of combined factor VII and factor XI deficiencies

Expression studies of key adipogenic transcriptional factors reveal that the anti-adipogenic properties of retinol in primary cultured human preadipocytes are due to retinol per se

The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal A{alpha} disulfide bonds in protein assembly and secretion

Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Leptin mediates a proliferative response in human MCF7 breast cancer cells

Direct in vitro effects of androgens and estrogens on ob gene expression and leptin secretion in human adipose tissue

Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K)

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency

Characterization of combined factor VII and factor XI deficiencies

Proadipogenic effect of leptin on rat preadipocytes in vitro: activation of MAPK and STAT3 signaling pathways

100 children treated by the combination of propionylerythromycin (in the form of the laurylsulfate) and trisulfazine. Granules suspended in a syrup

Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients

Significant decrease of the optical losses in the coupling between colloidal CdSe/CdS nanocrystals and a flat gold film at cryogenic temperature

Aide médicale à la procréation, malformations congénitales et santé postnatale

Unraveling the time cross correlations of an emitter switching between two states with the same fluorescence intensity

Enhanced and polarized emission from single colloidal CdSe/CdS nanocrystals coupled to a one-dimensional gold grating

LHX2 haploinsufficiency causes a variable neurodevelopmental disorder

Thermal activation of non-radiative Auger recombination in charged colloidal nanocrystals

Fetal costello syndrome with neuromuscular spindle excess and p.Gly12Val HRAS mutation

Clinical delineation of SETBP1 haploinsufficiency disorder

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

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