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...

Mutation screening of the muscarinic M 2 and M 3 receptor genes in normal and asthmatic subjects

British journal of pharmacology, 2009-01, Vol.133 (1), p.43-48

2009

Volltextzugriff (PDF)

Population Structure in the Mediterranean Basin: A Y Chromosome Perspective

Annals of human genetics, 2006-03, Vol.70 (2), p.207-225

2006

Volltextzugriff (PDF)

ESTUDO IN SILICO DAS LINHAGENS DE ENTEROCOCCUS FAECIUM: ANÁLISE PANGENÔMICA E PREDIÇÃO DE ALVOS VACINAIS E DE FÁRMACOS

Hematology, Transfusion and Cell Therapy, 2023-10, Vol.45, p.S837

2023

Volltextzugriff (PDF)

Novel Polymorphisms Influencing Transcription of the Human CHRM2 Gene in Airway Smooth Muscle

American journal of respiratory cell and molecular biology, 2004-05, Vol.30 (5), p.678-686

2004

Volltextzugriff (PDF)

Sleep Brain Networks and Sleep Depth during Somatosensory Stimulation

Klinische Neurophysiologie, 2013-03, Vol.44 (1)

2013

Volltextzugriff (PDF)

THE EFFECT OF VARIOUS RADIATION SHIELDS ON OPERATOR EXPOSURE DURING CONGENITAL CARDIAC CATHETERIZATION

Journal of the American College of Cardiology, 2014, Vol.63 (12), p.A522-A522

2014

Volltextzugriff (PDF)

Treatment of leg ulcers with platelet-derived wound healing factor (PDWHFS) in a patient with beta thalassaemia intermedia

British journal of haematology, 2001-02, Vol.112 (2), p.528-529

2001

Volltextzugriff (PDF)

Hb St. Luke's [alpha95(G2)Pro --> Arg (alpha1)]

Hemoglobin, 2003-05, Vol.27 (2), p.137-137

Felice, Alexander E

2003

Volltextzugriff (PDF)

Two new missense mutations (P134T and A244V) in the coagulation factor VII gene

Human mutation, 1998, Vol.11 (S1), p.S189-S191

1998

Volltextzugriff (PDF)

Polymerase chain reaction in molecular biotechnology ; appropriate technology for developing countries

World journal of microbiology & biotechnology, 1996-09, Vol.12 (5), p.467-471

1996

Volltextzugriff (PDF)

Characterization and locus assignment of two α-globin variants present in the maltese population: Hb St. Luke's [α95(G2)Pro→Arg] and Hb Setif [α94(G1)Asp→Tyr]

Hemoglobin, 1999, Vol.23 (2), p.145-157

1999

Volltextzugriff (PDF)

HB Setif [α94(GI)ASPàTYR] in Malta

Hemoglobin, 1997, Vol.21 (1), p.91-96

1997

Volltextzugriff (PDF)

Different ζ globin gene deletions among black Americans

Human genetics, 1986-07, Vol.73 (3), p.221-224

1986

Volltextzugriff (PDF)

α‐thalassemia among Pediatric Hemoglobin S Homozygotes: Molecular and Clinical Studies

Annals of the New York Academy of Sciences, 1989-01, Vol.565 (1), p.381-382

1989

Volltextzugriff (PDF)

Quantitation of erythropoietin stimulatory activity using [3H]thymidine uptake by K562 cells

Experimental hematology, 1989-02, Vol.17 (2), p.102-105

1989

Volltextzugriff (PDF)

Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia

American journal of hematology, 1987-08, Vol.25 (4), p.389-400

1987

Volltextzugriff (PDF)

Hemorheologic Parameters in Children with Homozygous Sickle Cell Anemia Receiving Chronic Red Cell Transfusions for Large Cerebral Vessel Vasculopathy

Annals of the New York Academy of Sciences, 1989-07, Vol.565 (1), p.455-457

1989

Volltextzugriff (PDF)

Partial deletion of the 5' beta-globin gene region causes beta zero- thalassemia in members of an American black family

Blood, 1984-10, Vol.64 (4), p.941-944

1984

Volltextzugriff (PDF)

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

Blood, 1984-05, Vol.63 (5), p.1253-1257

1984

Volltextzugriff (PDF)

Partial deletion of the 5' beta-globin gene region causes beta zero-thalassemia in members of an American black family

Blood, 1984-10, Vol.64 (4), p.941-944

1984

Volltextzugriff (PDF)

Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia

Hemoglobin, 1989, Vol.13 (6), p.557-566

1989

Volltextzugriff (PDF)

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

Blood, 1984-05, Vol.63 (5), p.1253-1257

1984

Volltextzugriff (PDF)

Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2

Biochemical genetics, 1982-08, Vol.20 (7-8), p.689-701

1982

Volltextzugriff (PDF)

The Atlanta family with hemoglobin grady revisited

American journal of human genetics, 1983-11, Vol.35 (6), p.1314-1316

1983

Volltextzugriff (PDF)

The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotes

American journal of clinical pathology, 1981-07, Vol.76 (1), p.70-73

1981

Volltextzugriff (PDF)

1 – 25 von 50

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(41)

Publikationsform

Artikel
(44)
Bücher
(6)

Sprache

Englisch
(45)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutation screening of the muscarinic M 2 and M 3 receptor genes in normal and asthmatic subjects

Population Structure in the Mediterranean Basin: A Y Chromosome Perspective

ESTUDO IN SILICO DAS LINHAGENS DE ENTEROCOCCUS FAECIUM: ANÁLISE PANGENÔMICA E PREDIÇÃO DE ALVOS VACINAIS E DE FÁRMACOS

Novel Polymorphisms Influencing Transcription of the Human CHRM2 Gene in Airway Smooth Muscle

Sleep Brain Networks and Sleep Depth during Somatosensory Stimulation

THE EFFECT OF VARIOUS RADIATION SHIELDS ON OPERATOR EXPOSURE DURING CONGENITAL CARDIAC CATHETERIZATION

Treatment of leg ulcers with platelet-derived wound healing factor (PDWHFS) in a patient with beta thalassaemia intermedia

Hb St. Luke's [alpha95(G2)Pro --> Arg (alpha1)]

Two new missense mutations (P134T and A244V) in the coagulation factor VII gene

Polymerase chain reaction in molecular biotechnology ; appropriate technology for developing countries

Characterization and locus assignment of two α-globin variants present in the maltese population: Hb St. Luke's [α95(G2)Pro→Arg] and Hb Setif [α94(G1)Asp→Tyr]

HB Setif [α94(GI)ASPàTYR] in Malta

Different ζ globin gene deletions among black Americans

α‐thalassemia among Pediatric Hemoglobin S Homozygotes: Molecular and Clinical Studies

Quantitation of erythropoietin stimulatory activity using [3H]thymidine uptake by K562 cells

Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia

Hemorheologic Parameters in Children with Homozygous Sickle Cell Anemia Receiving Chronic Red Cell Transfusions for Large Cerebral Vessel Vasculopathy

Partial deletion of the 5' beta-globin gene region causes beta zero- thalassemia in members of an American black family

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

Partial deletion of the 5' beta-globin gene region causes beta zero-thalassemia in members of an American black family

Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2

The Atlanta family with hemoglobin grady revisited

The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotes

Suchergebnisse filtern