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IL-12 initiates tumor rejection via lymphoid tissue-inducer cells bearing the natural cytotoxicity receptor NKp46

Nature immunology, 2010-11, Vol.11 (11), p.1030

2010

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A Woman with Missing Hb A 2 Due to a Novel (εγ)δβ 0 -Thalassemia and a Novel δ-Globin Variant Hb A 2 -Gebenstorf ( HBD : c.209G>A)

Hemoglobin, 2020-05, Vol.44 (3), p.214-217

2020

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A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Hemoglobin, 2020-05, Vol.44 (3), p.214-217

2020

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Two Novel α 2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2 : c.428A > T) and Severe ( HBA2 : c.342-345insCC) α -Thalassemia Phenotype

Hemoglobin, 2015-03, Vol.39 (2), p.144-146

2015

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Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

Hemoglobin, 2015-04, Vol.39 (2), p.144-146

2015

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A new (G)γ-globin variant causing low oxygen affinity: Hb F-Brugine/Feldkirch [(G)γ105(G7)Leu→His; HBG2: c.317T>A]

Hemoglobin, 2014, Vol.38 (2), p.84-87

2014

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A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]

Hemoglobin, 2014-04, Vol.38 (2), p.84-87

2014

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A Swiss (εγδβ)0‐thalassemia patient with a novel 3‐Mb deletion associated with mild mental impairment

American journal of hematology, 2013-02, Vol.88 (2), p.158-159

2013

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Neonatal cyanosis due to a new (G)γ-globin variant causing low oxygen affinity: Hb F-Sarajevo [(G)γ102(G4)Asn→Thr, AAC>ACC]

Hemoglobin, 2012-01, Vol.36 (2), p.109-113

2012

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Increased apoptosis induction by 121F mutant p53

The EMBO journal, 1999-08, Vol.18 (16), p.4424-4437

1999

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The transcriptional repressor Brinker antagonizes Wingless signaling

Genes & development, 2002-07, Vol.16 (14), p.1828-1838

2002

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Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels

Hemoglobin, 2012-04, Vol.36 (2), p.177-182

2012

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Direct competition between Brinker and Drosophila Mad in Dpp target gene transcription

EMBO reports, 2001-04, Vol.2 (4), p.298-305

2001

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Neonatal Cyanosis Due to A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Sarajevo [Gγ102(G4)Asn→Thr, AAC>ACC]

Hemoglobin, 2012-04, Vol.36 (2), p.109-113

2012

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Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A 2 Levels

Hemoglobin, 2012-04, Vol.36 (2), p.177-182

2012

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Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints But Causing Different Hb A(2) Levels: Gene rearrangement in the β-globin complex

Hemoglobin, 2012, Vol.36 (2), p.177-82

2012

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Identification of sulfate starvation-regulated genes in Escherichia coli: a gene cluster involved in the utilization of taurine as a sulfur source

Journal of Bacteriology, 1996-09, Vol.178 (18), p.5438-5446

1996

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Distinct expression patterns of the immunogenic differentiation antigen NY‐BR‐1 in normal breast, testis and their malignant counterparts

International journal of cancer, 2008-04, Vol.122 (7), p.1585-1591

2008

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Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels

Hemoglobin, 2012, Vol.36 (2), p.177-182

2012

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A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Hemoglobin, 2020, Vol.44 (3), p.214-217

2020

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Degradative pathways for p-toluenecarboxylate and p-toluenesulfonate and their multicomponent oxygenases in Comamonas testosteroni strains PSB-4 and T-2

Microbiology (Society for General Microbiology), 1996-09, Vol.142 ( Pt 9), p.2419

1996

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A Swiss (εγδβ)⁰-thalassemia patient with a novel 3-Mb deletion associated with mild mental impairment

American journal of hematology, 2013, Vol.88 (2), p.158-159

2013

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A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

Hematology reports, 2011, Vol.3 (3), p.e30-e30

2011

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Patients With Dupuytren Disease Use Excessive Grip Force When Lifting and Holding Small Objects, Independent of the Degree of Contracture

Archives of physical medicine and rehabilitation, 2023-08, Vol.104 (8), p.1268-1273

2023

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Differences in the Inflammatory Response of White Adipose Tissue and Adipose-Derived Stem Cells

International journal of molecular sciences, 2020-02, Vol.21 (3), p.1086

2020

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IL-12 initiates tumor rejection via lymphoid tissue-inducer cells bearing the natural cytotoxicity receptor NKp46

A Woman with Missing Hb A 2 Due to a Novel (εγ)δβ 0 -Thalassemia and a Novel δ-Globin Variant Hb A 2 -Gebenstorf ( HBD : c.209G>A)

A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Two Novel α 2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2 : c.428A > T) and Severe ( HBA2 : c.342-345insCC) α -Thalassemia Phenotype

Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

A new (G)γ-globin variant causing low oxygen affinity: Hb F-Brugine/Feldkirch [(G)γ105(G7)Leu→His; HBG2: c.317T>A]

A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]

A Swiss (εγδβ)0‐thalassemia patient with a novel 3‐Mb deletion associated with mild mental impairment

Neonatal cyanosis due to a new (G)γ-globin variant causing low oxygen affinity: Hb F-Sarajevo [(G)γ102(G4)Asn→Thr, AAC>ACC]

Increased apoptosis induction by 121F mutant p53

The transcriptional repressor Brinker antagonizes Wingless signaling

Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels

Direct competition between Brinker and Drosophila Mad in Dpp target gene transcription

Neonatal Cyanosis Due to A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Sarajevo [Gγ102(G4)Asn→Thr, AAC>ACC]

Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A 2 Levels

Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints But Causing Different Hb A(2) Levels: Gene rearrangement in the β-globin complex

Identification of sulfate starvation-regulated genes in Escherichia coli: a gene cluster involved in the utilization of taurine as a sulfur source

Distinct expression patterns of the immunogenic differentiation antigen NY‐BR‐1 in normal breast, testis and their malignant counterparts

Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels

A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Degradative pathways for p-toluenecarboxylate and p-toluenesulfonate and their multicomponent oxygenases in Comamonas testosteroni strains PSB-4 and T-2

A Swiss (εγδβ)⁰-thalassemia patient with a novel 3-Mb deletion associated with mild mental impairment

A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

Patients With Dupuytren Disease Use Excessive Grip Force When Lifting and Holding Small Objects, Independent of the Degree of Contracture

Differences in the Inflammatory Response of White Adipose Tissue and Adipose-Derived Stem Cells

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