UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Relationships between DNA methylation and expression in erythrocyte membrane protein (band 3, protein 4.2, and β-spectrin) genes during human erythroid development and differentiation

International journal of hematology, 2005-12, Vol.82 (5), p.422-429

2005

Volltextzugriff (PDF)

Ankyrin gene mutations in Japanese patients with hereditary spherocytosis

International journal of hematology, 2001-01, Vol.73 (1), p.54-63

2001

Volltextzugriff (PDF)

DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders

International journal of hematology, 2005-06, Vol.81 (5), p.385-395

2005

Volltextzugriff (PDF)

Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation

The Journal of clinical investigation, 1996-04, Vol.97 (8), p.1804-1817

1996

Volltextzugriff (PDF)

Protein 4.2： Normal and Abnormal in Clinical Hematology, Protein Chemistry, Molecular Genetics, and Ultrastructure

KAWASAKI MEDICAL JOURNAL, 2000, Vol.26 (2), p.35-82

2000

Volltextzugriff (PDF)

Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population

International journal of hematology, 2000-02, Vol.71 (2), p.118-135

2000

Volltextzugriff (PDF)

A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele 4.1 Madrid) : Implications regarding a critical role of protein 4.1 in maintenance of the integrity of the red blood cell membrane

Blood, 1997-09, Vol.90 (6), p.2471-2481

1997

Volltextzugriff (PDF)

A Markedly Disrupted Skeletal Network With Abnormally Distributed Intramembrane Particles in Complete Protein 4.1-Deficient Red Blood Cells (Allele 4.1 Madrid): Implications Regarding a Critical Role of Protein 4.1 in Maintenance of the Integrity of the Red Blood Cell Membrane

Blood, 1997-09, Vol.90 (6), p.2471-2481

1997

Volltextzugriff (PDF)

Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene

Experimental hematology, 1999, Vol.27 (1), p.54-62

1999

Volltextzugriff (PDF)

Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near‐normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency

British journal of haematology, 1998-09, Vol.102 (4), p.932-939

1998

Volltextzugriff (PDF)

A Case of Insulin-dependent Diabetes Mellitus (IDDM) Caused by EB Virus Infection Accompanied by Atypical (nontuberculous) Mycobacterial Infection

Journal of the Japan Diabetes Society, 1996/10/30, Vol.39(10), pp.803-808

1996

Volltextzugriff (PDF)

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis

British journal of haematology, 1997-12, Vol.99 (3), p.522-530

1997

Volltextzugriff (PDF)

Genotypic and phenotypic expressions of protein 4.2 in human erythroid cells

Gene function & disease, 2000-09, Vol.1 (2), p.61-81

2000

Volltextzugriff (PDF)

Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied

Hematology (Luxembourg), 2001-01, Vol.6 (6), p.399-422

2001

Volltextzugriff (PDF)

Band 4.2 Shiga: 317 CGC → TGC in compound heterozygotes with 142 GCT → ACT results in band 4.2 deficiency and microspherocytosis

British journal of haematology, 1995-10, Vol.91 (2), p.333-340

1995

Volltextzugriff (PDF)

Stop codon in exon 30 (E2069X) of β-spectrin gene associated with hereditary elliptocytosis in spectrin Nagoya

Human mutation, 1996, Vol.8 (4), p.366-368

1996

Volltextzugriff (PDF)

Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population

International journal of hematology, 1994-12, Vol.60 (4), p.227-238

1994

Volltextzugriff (PDF)

Band 4.2 Komatsu: 523 GAT→TAT (175 Asp→Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2 hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network

International journal of hematology, 1995-06, Vol.61 (4), p.165-178

1995

Volltextzugriff (PDF)

The state of DNA methylation in the promoter regions of the human red cell membrane protein (band 3, protein 4.2, and β-spectrin) genes

Gene function & disease, 2001-12, Vol.2 (4), p.171-184

2001

Volltextzugriff (PDF)

Generalized Resistance to Thyroid Hormone (GRTH) in a Family: Case Studies

Endocrinologia Japonica, 1992, Vol.39(6), pp.533-538

1992

Volltextzugriff (PDF)

Hereditary elliptocytosis associated with spectrin Le Puy in a Japanese family: Ultrastructural aspect of the red cell skeleton

European journal of haematology, 1994-02, Vol.52 (2), p.92-98

1994

Volltextzugriff (PDF)

インスリン非依存型糖尿病ヒト膵島におけるProinsulin, Insulinの局在に関する免疫組織学的研究

川崎医学会誌, 1993, Vol.19 (4), p.283-292

八幡愛弓

1993

Volltextzugriff (PDF)

Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells

Cell motility and the cytoskeleton, 1996, Vol.33 (2), p.95-105

1996

Volltextzugriff (PDF)

出産後にインスリン依存型糖尿病(IDDM)とGraves病を同時に発症した1例

川崎医学会誌, 1995, Vol.21 (4), p.297-301

1995

Volltextzugriff (PDF)

糖尿病合併症におけるトロンボモジュリン測定の有用性

川崎医学会誌, 1993, Vol.19 (1), p.19-24

1993

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(30)

Sprache

Englisch
(25)
Japanisch
(9)

Erscheinungsjahr

n.n

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Relationships between DNA methylation and expression in erythrocyte membrane protein (band 3, protein 4.2, and β-spectrin) genes during human erythroid development and differentiation

Ankyrin gene mutations in Japanese patients with hereditary spherocytosis

DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders

Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation

Protein 4.2： Normal and Abnormal in Clinical Hematology, Protein Chemistry, Molecular Genetics, and Ultrastructure

Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population

A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele 4.1 Madrid) : Implications regarding a critical role of protein 4.1 in maintenance of the integrity of the red blood cell membrane

A Markedly Disrupted Skeletal Network With Abnormally Distributed Intramembrane Particles in Complete Protein 4.1-Deficient Red Blood Cells (Allele 4.1 Madrid): Implications Regarding a Critical Role of Protein 4.1 in Maintenance of the Integrity of the Red Blood Cell Membrane

Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene

Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near‐normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency

A Case of Insulin-dependent Diabetes Mellitus (IDDM) Caused by EB Virus Infection Accompanied by Atypical (nontuberculous) Mycobacterial Infection

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis

Genotypic and phenotypic expressions of protein 4.2 in human erythroid cells

Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied

Band 4.2 Shiga: 317 CGC → TGC in compound heterozygotes with 142 GCT → ACT results in band 4.2 deficiency and microspherocytosis

Stop codon in exon 30 (E2069X) of β-spectrin gene associated with hereditary elliptocytosis in spectrin Nagoya

Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population

Band 4.2 Komatsu: 523 GAT→TAT (175 Asp→Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2 hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network

The state of DNA methylation in the promoter regions of the human red cell membrane protein (band 3, protein 4.2, and β-spectrin) genes

Generalized Resistance to Thyroid Hormone (GRTH) in a Family: Case Studies

Hereditary elliptocytosis associated with spectrin Le Puy in a Japanese family: Ultrastructural aspect of the red cell skeleton

インスリン非依存型糖尿病ヒト膵島におけるProinsulin, Insulinの局在に関する免疫組織学的研究

Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells

出産後にインスリン依存型糖尿病(IDDM)とGraves病を同時に発症した1例

糖尿病合併症におけるトロンボモジュリン測定の有用性

Suchergebnisse filtern