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Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3

Blood, 2000-08, Vol.96 (4), p.1602-1604

2000

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Truncated Hemoglobins in Actinorhizal Nodules of Datisca glomerata

Plant biology (Stuttgart, Germany), 2007-11, Vol.9 (6), p.776-785

2007

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Frankia alni Symbiotic Transcriptome

Molecular plant-microbe interactions, 2010-05, Vol.23 (5), p.593-607

2010

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Evidence That Red Blood Cell Protein p55 May Participate in the Skeleton-Membrane Linkage That Involves Protein 4.1 and Glycophorin C

Blood, 1993-08, Vol.82 (4), p.1323-1327

1993

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Early signaling in actinorhizal symbioses

Plant signaling & behavior, 2011-09, Vol.6 (9), p.1377-1379

2011

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The Cisternae Decorating the Red Blood Cell Membrane in Congenital Dyserythropoietic Anemia (Type II) Originate From the Endoplasmic Reticulum

Blood, 1996-05, Vol.87 (10), p.4433-4439

1996

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Rare specific flavonoids affect differentially compatible and incompatible strains in the Myrica gale-Frankia actinorhizal symbiosis

Applied and environmental microbiology, 2010, Vol.76, p.2451-2460

2010

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A Deletional Frameshift Mutation in Protein 4.2 Gene (Allele 4.2 Lisboa) Associated With Hereditary Hemolytic Anemia

Blood, 1995-01, Vol.85 (1), p.250-256

1995

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Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis

British journal of haematology, 1996-06, Vol.93 (4), p.828-834

1996

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Two distinct truncated variants of ankyrin associated with hereditary spherocytosis

American journal of hematology, 1998-05, Vol.58 (1), p.36-41

1998

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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

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Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

American journal of hematology, 1997-03, Vol.54 (3), p.242-248

1997

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Les surdités génétiques : première cause de surdité de perception de l’enfant

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2001-03, Vol.8 (3), p.308-312

2001

Volltextzugriff (PDF)

Genetic deafness:the primary cause of sensorineural hearing loss in children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2001-03, Vol.8 (3), p.308-312

2001

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Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin

British journal of haematology, 1993-01, Vol.83 (1), p.152-157

1993

Volltextzugriff (PDF)

Elliptopoikilocytosis Associated With the α469 His → Pro Mutation in Spectrin Barcelona (αI/50-46b)

Blood, 1993-09, Vol.82 (5), p.1661-1665

1993

Volltextzugriff (PDF)

Hereditary spherocytosis: from clinical to molecular defects

Haematologica (Roma), 1998-03, Vol.83 (3), p.240

1998

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Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis

British journal of haematology, 1989-01, Vol.71 (1), p.141-146

1989

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)

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

Blood, 1993-08, Vol.82 (4), p.1323-1327

1993

Volltextzugriff (PDF)

Expression of spectrin mutations as a function of their topography

Biochemical Society transactions, 1992-11, Vol.20 (4), p.782

1992

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Spectrin beta-chain variant associated with hereditary elliptocytosis

The Journal of clinical investigation, 1982-10, Vol.70 (4), p.707-715

1982

Volltextzugriff (PDF)

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 mutations in hereditary elliptocytosis and hereditary spherocytosis

Human mutation, 1996, Vol.8 (2), p.97-107

1996

Volltextzugriff (PDF)

Assignment of SpαI/74 Hereditary Elliptocytosis to the α- or β-Chain of Spectrin Through In Vitro Dimer Reconstitution

Blood, 1990-05, Vol.75 (10), p.2061-2069

1990

Volltextzugriff (PDF)

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Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3

Truncated Hemoglobins in Actinorhizal Nodules of Datisca glomerata

Frankia alni Symbiotic Transcriptome

Evidence That Red Blood Cell Protein p55 May Participate in the Skeleton-Membrane Linkage That Involves Protein 4.1 and Glycophorin C

Early signaling in actinorhizal symbioses

The Cisternae Decorating the Red Blood Cell Membrane in Congenital Dyserythropoietic Anemia (Type II) Originate From the Endoplasmic Reticulum

Rare specific flavonoids affect differentially compatible and incompatible strains in the Myrica gale-Frankia actinorhizal symbiosis

A Deletional Frameshift Mutation in Protein 4.2 Gene (Allele 4.2 Lisboa) Associated With Hereditary Hemolytic Anemia

Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis

Two distinct truncated variants of ankyrin associated with hereditary spherocytosis

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

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

Les surdités génétiques : première cause de surdité de perception de l’enfant

Genetic deafness:the primary cause of sensorineural hearing loss in children

Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin

Elliptopoikilocytosis Associated With the α469 His → Pro Mutation in Spectrin Barcelona (αI/50-46b)

Hereditary spherocytosis: from clinical to molecular defects

Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis

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

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

Expression of spectrin mutations as a function of their topography

Spectrin beta-chain variant associated with hereditary elliptocytosis

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

Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis

Assignment of SpαI/74 Hereditary Elliptocytosis to the α- or β-Chain of Spectrin Through In Vitro Dimer Reconstitution

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