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Dépistage néonatal et configuration de sujets éthiques: une analyse sociohistorique : Prédiction et prévention

Éthique & santé, 2012, Vol.9 (2), p.76-80

VAILLY, J

2012

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Dépistage néonatal et configuration de sujets éthiques : une analyse sociohistorique

Éthique & santé, 2012-06, Vol.9 (2), p.76-80

Vailly, J.

2012

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The Birth of a Genetics Policy: Social Issues of Newborn Screening

Vailly, Joëlle

1, 2013

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Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia

Gene therapy, 1998-10, Vol.5 (10), p.1322-1332

1998

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Splicing Modulation of Integrin (β4 Pre-mRNA Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing

Human molecular genetics, 1999-10, Vol.8 (11), p.2097-2105

1999

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Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence

Journal of investigative dermatology, 1995-04, Vol.104 (4), p.462-466

1995

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The Genes for Nicein/Kalinin 125- and 100-kDa Subunits, Candidates for Junctional Epidermolysis Bullosa, Map to Chromosomes 1q32 and 1q25-q31

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.286-288

1994

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

Nature genetics, 1994-03, Vol.6 (3), p.299-304

1994

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Biomedical arguments and modes of action around an a priori health policy: neonatal screening for cystic fibrosis in Brittany

Sciences sociales et santé, 2004-12, Vol.22 (4), p.35-60

Vailly, Joelle

2004

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Identification of a Homozygous Exon-Skipping Mutation in the LAMC2 Gene in a Patient with Herlitz's Junctional Epidermolysis Bullosa

Journal of investigative dermatology, 1995-03, Vol.104 (3), p.434-437

1995

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Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa

Human gene therapy, 1998-06, Vol.9 (9), p.1359-1370

1998

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)

Nature genetics, 1994-03, Vol.6 (3), p.299-304

1994

Volltextzugriff (PDF)

Splicing modulation of integrin beta 4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Human molecular genetics, 1999-10, Vol.8 (11), p.2097-2105

1999

Volltextzugriff (PDF)

Functional re-expression of laminin-5 in laminin- gamma 2-deficient human keratinocytes modifies cell morphology, motility, and adhesion

The Journal of biological chemistry, 1996-08, Vol.271 (31), p.18437-18444

1996

Volltextzugriff (PDF)

Extending Abnormality

The Birth of a Genetics Policy, 2013, p.119-142

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

Living with the Disease

The Birth of a Genetics Policy, 2013, p.143-168

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

Maintaining a Quality Life

The Birth of a Genetics Policy, 2013, p.169-195

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

On Scientific Grounds

The Birth of a Genetics Policy, 2013, p.57-85

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

The Birth of a Screening Policy (Brittany-France)

The Birth of a Genetics Policy, 2013, p.21-55

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

Governing

The Birth of a Genetics Policy, 2013, p.87-118

Vailly, Joëlle

1, 2013

Volltextzugriff (PDF)

Persistence and transmission in the mouse of autonomous plasmids derived from polyoma virus

Cold Spring Harbor Symposia on Quantitative Biology, 1985, Vol.50, p.679

1985

Volltextzugriff (PDF)

Splicing modulation of integrin beta4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Human molecular genetics, 1999-10, Vol.8 (11), p.2097-2105

1999

Volltextzugriff (PDF)

Splicing modulation of integrin [beta]4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Human molecular genetics, 1999-10, Vol.8 (11), p.2097

1999

Volltextzugriff (PDF)

Functional Re-expression of laminin-5 in laminin-gamma2-deficient human keratinocytes modifies cell morphology, motility, and adhesion

The Journal of biological chemistry, 1996-08, Vol.271 (31), p.18437-18444

1996

Volltextzugriff (PDF)

Germ line transmission of autonomous genetic elements in transgenic mouse strains

Cell, 1986-08, Vol.46 (4), p.513-519

1986

Volltextzugriff (PDF)

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Dépistage néonatal et configuration de sujets éthiques: une analyse sociohistorique : Prédiction et prévention

Dépistage néonatal et configuration de sujets éthiques : une analyse sociohistorique

The Birth of a Genetics Policy: Social Issues of Newborn Screening

Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia

Splicing Modulation of Integrin (β4 Pre-mRNA Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing

Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence

The Genes for Nicein/Kalinin 125- and 100-kDa Subunits, Candidates for Junctional Epidermolysis Bullosa, Map to Chromosomes 1q32 and 1q25-q31

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

Biomedical arguments and modes of action around an a priori health policy: neonatal screening for cystic fibrosis in Brittany

Identification of a Homozygous Exon-Skipping Mutation in the LAMC2 Gene in a Patient with Herlitz's Junctional Epidermolysis Bullosa

Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)

Splicing modulation of integrin beta 4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Functional re-expression of laminin-5 in laminin- gamma 2-deficient human keratinocytes modifies cell morphology, motility, and adhesion

Extending Abnormality

Living with the Disease

Maintaining a Quality Life

On Scientific Grounds

The Birth of a Screening Policy (Brittany-France)

Governing

Persistence and transmission in the mouse of autonomous plasmids derived from polyoma virus

Splicing modulation of integrin beta4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Splicing modulation of integrin [beta]4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing

Functional Re-expression of laminin-5 in laminin-gamma2-deficient human keratinocytes modifies cell morphology, motility, and adhesion

Germ line transmission of autonomous genetic elements in transgenic mouse strains

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