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The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

Leukemia, 2018-04, Vol.32 (4), p.911-919

2018

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The Cul4A-DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity

Oncogene, 2013-09, Vol.32 (39), p.4721-4726

2013

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Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Circulation research, 2001-04, Vol.88 (7), p.740-745

2001

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Peopling of three Mediterranean Islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability

American journal of physical anthropology, 2003-07, Vol.121 (3), p.270-279

2003

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FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Cell, 2003-06, Vol.113 (7), p.829-840

2003

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Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Human immunology, 2001-09, Vol.62 (9), p.871-884

2001

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2001-01, Vol.103 (2), p.196-200

2001

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Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2002-07, Vol.106 (1), p.69-74

2002

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Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

Journal of cellular physiology, 2002-01, Vol.190 (1), p.1-6

2002

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Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Annals of human genetics, 2000-09, Vol.64 (5), p.395-412

2000

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Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes

The Journal of biological chemistry, 2001-08, Vol.276 (33), p.30623-30630

2001

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Brugada syndrome and sudden cardiac death in children

The Lancet (British edition), 2000-03, Vol.355 (9206), p.808-809

2000

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Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

American journal of human biology, 2003-03, Vol.15 (2), p.151-163

2003

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Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome

American journal of physiology. Heart and circulatory physiology, 2000-10, Vol.279 (4), p.H1748-H1756

2000

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β-Thalassemia Mutations in Corsica

Hemoglobin, 2000-01, Vol.24 (3), p.239-244

2000

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Mechanisms of I(Ks) suppression in LQT1 mutants

American journal of physiology. Heart and circulatory physiology, 2000-12, Vol.279 (6), p.H3003

2000

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Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.613-619

2004

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A study of several genetic markers in the Corsican population (France)

Anthropologischer Anzeiger, 1995-06, Vol.53 (2), p.125

1995

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Finger dermatoglyphics in the Corsican population (France)

Anthropologischer Anzeiger, 1999-12, Vol.57 (4), p.339

1999

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The polymorphism of the APOB 3' VNTR in the populations of the three largest islands of the western Mediterranean

Anthropologischer Anzeiger, 1998-09, Vol.56 (3), p.227

1998

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β-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations

Human biology, 2003-12, Vol.75 (6), p.855-871

2003

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Study on the variability of seven genetic serum protein markers in Corsica (France)

Anthropologischer Anzeiger, 1996-06, Vol.54 (2), p.97

1996

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Mitochondrial DNA sequence analysis in Sicily

American journal of human biology, 2001-09, Vol.13 (5), p.576-589

2001

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Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

Journal of medical genetics, 1998-09, Vol.35 (9), p.778-783

1998

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A pentanucleotide repeat polymorphism (TTTTA) in the apolipoprotein (a) gene--its distribution and its association with the risk of cardiovascular disease

Collegium antropologicum, 2003-06, Vol.27 (1), p.105-115

2003

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The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

The Cul4A-DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity

Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Peopling of three Mediterranean Islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes

Brugada syndrome and sudden cardiac death in children

Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome

β-Thalassemia Mutations in Corsica

Mechanisms of I(Ks) suppression in LQT1 mutants

Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region

A study of several genetic markers in the Corsican population (France)

Finger dermatoglyphics in the Corsican population (France)

The polymorphism of the APOB 3' VNTR in the populations of the three largest islands of the western Mediterranean

β-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations

Study on the variability of seven genetic serum protein markers in Corsica (France)

Mitochondrial DNA sequence analysis in Sicily

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

A pentanucleotide repeat polymorphism (TTTTA) in the apolipoprotein (a) gene--its distribution and its association with the risk of cardiovascular disease

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