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Dual Role of Dendritic Cells in the Induction and Down-Regulation of Antigen-Specific Cutaneous Inflammation

The Journal of immunology (1950), 1998-02, Vol.160 (3), p.1181-1190

1998

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Contact dermatitis. I. Pathophysiology of contact sensitivity

EJD. European journal of dermatology, 1999, Vol.9 (1), p.65-77

1999

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Cytotoxicity is mandatory for CD8(+) T cell-mediated contact hypersensitivity

The Journal of experimental medicine, 1999-03, Vol.189 (5), p.779-786

1999

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The popliteal lymph node response to streptozotocin is under type 1, MHC class-I restricted, CD8 + T-cell control

Toxicology (Amsterdam), 2000-04, Vol.146 (1), p.73-82

2000

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Interferon-γ Production in Skin During Contact Hypersensitivity. No Contribution from Keratinocytes

Journal of investigative dermatology, 2001-07, Vol.117 (1), p.163-163

2001

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Contact dermatitis. II. Clinical aspects and diagnosis

EJD. European journal of dermatology, 1999-03, Vol.9 (2), p.144-159

1999

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Increased production of interferon-gamma, but not IL-4 mRNA, by streptozotocin in the popliteal lymph node assay

Journal of applied toxicology, 2000-05, Vol.20 (3), p.175-178

2000

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Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

The Journal of clinical investigation, 1992-11, Vol.90 (5), p.1713-1717

1992

Volltextzugriff (PDF)

Molecular Analysis of Hereditary Elliptocytosis With Reduced Protein 4.1 in the French Northern Alps

Blood, 1991-10, Vol.78 (8), p.2113-2119

1991

Volltextzugriff (PDF)

Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

British journal of haematology, 1991-05, Vol.78 (1), p.108-113

1991

Volltextzugriff (PDF)

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

The Journal of clinical investigation, 1991-06, Vol.87 (6), p.2169-2177

1991

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Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton

The Journal of clinical investigation, 1994-10, Vol.94 (4), p.1651-1656

1994

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Spectrin Tunis (αI/78): A New αI Variant That Causes Asymptomatic Hereditary Elliptocytosis in the Heterozygous State

Blood, 1988-02, Vol.71 (2), p.508-511

1988

Volltextzugriff (PDF)

Spectrin Oran (αII/21), a new spectrin variant concerning the αII domain and causing severe elliptocytosis in the homozygous state

Blood, 1988-04, Vol.71 (4), p.1039-1047

1988

Volltextzugriff (PDF)

Diffusion of a particular 4.1(-) hereditary elliptocytosis allele in the French Northern Alps

Journal of biosocial science, 1993-04, Vol.25 (2), p.239

1993

Volltextzugriff (PDF)

Gerbich reactivity in 4.1(—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency

British journal of haematology, 1987-01, Vol.65 (1), p.43-50

1987

Volltextzugriff (PDF)

Spectrin nice (β220/216): a shortened β-chain variant associated with an increase of the αI/74 fragment in a case of elliptocytosis

Blood, 1987-06, Vol.69 (6), p.1759-1765

1987

Volltextzugriff (PDF)

Skin Inflammation During Contact Hypersensitivity Is Mediated by Early Recruitment of CD8+ T Cytotoxic 1 Cells Inducing Keratinocyte Apoptosis

The Journal of immunology (1950), 2002-03, Vol.168 (6), p.3079-3087

2002

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SpαI/65 Hereditary elliptocytosis in North Africa

American journal of hematology, 1986-10, Vol.23 (2), p.113-122

1986

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Spectrin Jendouba : an αII/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site

Blood, 1992-08, Vol.80 (3), p.809-815

1992

Volltextzugriff (PDF)

Evidence that expression of SpαI/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous α-spectrin allele

Human genetics, 1990-10, Vol.85 (6), p.627-630

1990

Volltextzugriff (PDF)

Two distinct variants of erythrocyte spectrin βIV domain

Human genetics, 1989-11, Vol.83 (4), p.373-376

1989

Volltextzugriff (PDF)

Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia

British journal of haematology, 1987-07, Vol.66 (3), p.393-400

1987

Volltextzugriff (PDF)

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

British journal of haematology, 1990-07, Vol.75 (3), p.414-420

1990

Volltextzugriff (PDF)

αI/65 hereditary elliptocytosis in Southern Italy : evidence for an African origin

Human genetics, 1992-07, Vol.89 (5), p.553-556

1992

Volltextzugriff (PDF)

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Dual Role of Dendritic Cells in the Induction and Down-Regulation of Antigen-Specific Cutaneous Inflammation

Contact dermatitis. I. Pathophysiology of contact sensitivity

Cytotoxicity is mandatory for CD8(+) T cell-mediated contact hypersensitivity

The popliteal lymph node response to streptozotocin is under type 1, MHC class-I restricted, CD8 + T-cell control

Interferon-γ Production in Skin During Contact Hypersensitivity. No Contribution from Keratinocytes

Contact dermatitis. II. Clinical aspects and diagnosis

Increased production of interferon-gamma, but not IL-4 mRNA, by streptozotocin in the popliteal lymph node assay

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

Molecular Analysis of Hereditary Elliptocytosis With Reduced Protein 4.1 in the French Northern Alps

Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton

Spectrin Tunis (αI/78): A New αI Variant That Causes Asymptomatic Hereditary Elliptocytosis in the Heterozygous State

Spectrin Oran (αII/21), a new spectrin variant concerning the αII domain and causing severe elliptocytosis in the homozygous state

Diffusion of a particular 4.1(-) hereditary elliptocytosis allele in the French Northern Alps

Gerbich reactivity in 4.1(—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency

Spectrin nice (β220/216): a shortened β-chain variant associated with an increase of the αI/74 fragment in a case of elliptocytosis

Skin Inflammation During Contact Hypersensitivity Is Mediated by Early Recruitment of CD8+ T Cytotoxic 1 Cells Inducing Keratinocyte Apoptosis

SpαI/65 Hereditary elliptocytosis in North Africa

Spectrin Jendouba : an αII/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site

Evidence that expression of SpαI/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous α-spectrin allele

Two distinct variants of erythrocyte spectrin βIV domain

Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

αI/65 hereditary elliptocytosis in Southern Italy : evidence for an African origin

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