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...

Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing

Proceedings of the National Academy of Sciences - PNAS, 2018-07, Vol.115 (31), p.E7379-E7388

2018

Volltextzugriff (PDF)

Clade F AAVHSCs cross the blood brain barrier and transduce the central nervous system in addition to peripheral tissues following intravenous administration in nonhuman primates

PloS one, 2019-11, Vol.14 (11), p.e0225582-e0225582

2019

Volltextzugriff (PDF)

Inhibition of Choroidal Neovascularization in a Nonhuman Primate Model by Intravitreal Administration of an AAV2 Vector Expressing a Novel Anti-VEGF Molecule

Molecular therapy, 2011-02, Vol.19 (2), p.260-265

2011

Volltextzugriff (PDF)

Sustained Correction of a Murine Model of Phenylketonuria following a Single Intravenous Administration of AAVHSC15-PAH

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.568-580

2020

Volltextzugriff (PDF)

Aurintricarboxylic acid increases yield of HSV-1 vectors

Molecular therapy. Methods & clinical development, 2014-01, Vol.1 (C), p.6-6, Article 6

2014

Volltextzugriff (PDF)

AAVHSC characterization for developing treatments for human genetic diseases of the nervous system

Molecular genetics and metabolism, 2020-02, Vol.129 (2), p.S62-S62

2020

Volltextzugriff (PDF)

Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAHenu2 mouse model

Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.S56-S56

2019

Volltextzugriff (PDF)

Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAH mouse model

Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.S56

2019

Volltextzugriff (PDF)

Low Seroprevalence of Neutralizing Antibodies Targeting Two Clade F AAV in Humans

Human gene therapy. Clinical development, 2018-03, Vol.29 (1), p.60-67

2018

Volltextzugriff (PDF)

Low Seroprevalence of Neutralizing Antibodies Targeting Two Clade F AAV in Humans

Human gene therapy. Clinical development, 2018-02, Article hum.2017.239

2018

Volltextzugriff (PDF)

Deletion in Erythrocyte Band 3 Gene in Malaria-Resistant Southeast Asian Ovalocytosis

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (24), p.11022-11026

1991

Volltextzugriff (PDF)

The Structure and Organization of the Human Erythroid Anion Exchanger (AE1) Gene

Genomics (San Diego, Calif.), 1994-12, Vol.24 (3), p.491-501

1994

Volltextzugriff (PDF)

Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger

The Journal of biological chemistry, 1998-03, Vol.273 (11), p.6380-6388

1998

Volltextzugriff (PDF)

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

Blood, 1996-12, Vol.88 (11), p.4366-4374

1996

Volltextzugriff (PDF)

883. AAV-2 Based Gene Therapy Using Novel Anti-VEGF Molecules for Inhibition of Angiogenesis in the Eye

Molecular therapy, 2006-05, Vol.13 (S1), p.S340-S340

2006

Volltextzugriff (PDF)

Mutations of Conserved Arginines in the Membrane Domain of Erythroid Band 3 Lead to a Decrease in Membrane-Associated Band 3 and to the Phenotype of Hereditary Spherocytosis

Blood, 1995-02, Vol.85 (3), p.634-640

1995

Volltextzugriff (PDF)

Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)

The Journal of clinical investigation, 1994, Vol.93 (1), p.121-130

1994

Volltextzugriff (PDF)

The Homozygous State for the Band 3 Protein Mutation in Southeast Asian Ovalocytosis May Be Lethal

Blood, 1994-11, Vol.84 (10), p.3590-3591

1994

Volltextzugriff (PDF)

A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis

The Journal of clinical investigation, 1995-03, Vol.95 (3), p.941-947

1995

Volltextzugriff (PDF)

Comparison of the Ankyrin (AC)n Microsatellites in Genomic DNA and mRNA Reveals Absence of One Ankyrin mRNA Allele in 20% of Patients With Hereditary Spherocytosis

Blood, 1995-06, Vol.85 (11), p.3278-3282

1995

Volltextzugriff (PDF)

Bone marrow stromal cell-mediated gene therapy for hemophilia A: in vitro expression of human factor VIII with high biological activity requires the inclusion of the proteolytic site at amino acid 1648

Human gene therapy, 1999-01, Vol.10 (1), p.61-76

1999

Volltextzugriff (PDF)

Band 3 memphis : a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG→GAG (Lys→Glu) in codon 56

Blood, 1992-09, Vol.80 (6), p.1592-1598

1992

Volltextzugriff (PDF)

Band 3 Tuscaloosa: Pro327 → Arg327 Substitution in the Cytoplasmic Domain of Erythrocyte Band 3 Protein Associated With Spherocytic Hemolytic Anemia and Partial Deficiency of Protein 4.2

Blood, 1992-07, Vol.80 (2), p.523-529

1992

Volltextzugriff (PDF)

Autosomal Dominant Distal Renal Tubular Acidosis Is Associated in Three Families with Heterozygosity for the R589H Mutation in the AE1 (Band 3) Clâ/HCO3 âExchanger

The Journal of biological chemistry, 1998-03, Vol.273 (11), p.6380

1998

Volltextzugriff (PDF)

1 – 25 von 34

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(30)

Publikationsform

Artikel
(34)

Sprache

Englisch
(34)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing

Clade F AAVHSCs cross the blood brain barrier and transduce the central nervous system in addition to peripheral tissues following intravenous administration in nonhuman primates

Inhibition of Choroidal Neovascularization in a Nonhuman Primate Model by Intravitreal Administration of an AAV2 Vector Expressing a Novel Anti-VEGF Molecule

Sustained Correction of a Murine Model of Phenylketonuria following a Single Intravenous Administration of AAVHSC15-PAH

Aurintricarboxylic acid increases yield of HSV-1 vectors

AAVHSC characterization for developing treatments for human genetic diseases of the nervous system

Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAHenu2 mouse model

Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAH mouse model

Low Seroprevalence of Neutralizing Antibodies Targeting Two Clade F AAV in Humans

Low Seroprevalence of Neutralizing Antibodies Targeting Two Clade F AAV in Humans

Deletion in Erythrocyte Band 3 Gene in Malaria-Resistant Southeast Asian Ovalocytosis

The Structure and Organization of the Human Erythroid Anion Exchanger (AE1) Gene

Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

883. AAV-2 Based Gene Therapy Using Novel Anti-VEGF Molecules for Inhibition of Angiogenesis in the Eye

Mutations of Conserved Arginines in the Membrane Domain of Erythroid Band 3 Lead to a Decrease in Membrane-Associated Band 3 and to the Phenotype of Hereditary Spherocytosis

Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)

The Homozygous State for the Band 3 Protein Mutation in Southeast Asian Ovalocytosis May Be Lethal

A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis

Comparison of the Ankyrin (AC)n Microsatellites in Genomic DNA and mRNA Reveals Absence of One Ankyrin mRNA Allele in 20% of Patients With Hereditary Spherocytosis

Bone marrow stromal cell-mediated gene therapy for hemophilia A: in vitro expression of human factor VIII with high biological activity requires the inclusion of the proteolytic site at amino acid 1648

Band 3 memphis : a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG→GAG (Lys→Glu) in codon 56

Band 3 Tuscaloosa: Pro327 → Arg327 Substitution in the Cytoplasmic Domain of Erythrocyte Band 3 Protein Associated With Spherocytic Hemolytic Anemia and Partial Deficiency of Protein 4.2

Autosomal Dominant Distal Renal Tubular Acidosis Is Associated in Three Families with Heterozygosity for the R589H Mutation in the AE1 (Band 3) Clâ/HCO3 âExchanger

Informing the Tolerability of Cancer Treatments Using Patient-Reported Outcome Measures: Summary of an FDA and Critical Path Institute Workshop

Suchergebnisse filtern