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...

Erythrocytosis and Pulmonary Hypertension in a Mouse Model of Human HIF2A Gain of Function Mutation

The Journal of biological chemistry, 2013-06, Vol.288 (24), p.17134-17144

2013

Volltextzugriff (PDF)

Recessive congenital methaemoglobinaemia: cytochrome b5 reductase deficiency

British journal of haematology, 2008-05, Vol.141 (3), p.298-308

2008

Volltextzugriff (PDF)

A Family with Erythrocytosis Establishes a Role for Prolyl Hydroxylase Domain Protein 2 in Oxygen Homeostasis

Proceedings of the National Academy of Sciences - PNAS, 2006-01, Vol.103 (3), p.654-659

2006

Volltextzugriff (PDF)

A Knock-in Mouse Model of Human PHD2 Gene-associated Erythrocytosis Establishes a Haploinsufficiency Mechanism

The Journal of biological chemistry, 2013-11, Vol.288 (47), p.33571-33584

2013

Volltextzugriff (PDF)

A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove

Blood, 2007-09, Vol.110 (6), p.2193-2196

2007

Volltextzugriff (PDF)

Mutation of von Hippel-Lindau tumour suppressor and human cardiopulmonary physiology

PLoS medicine, 2006-07, Vol.3 (7), p.e290

2006

Volltextzugriff (PDF)

The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms

Blood, 2010-06, Vol.115 (22), p.4517-4523

2010

Volltextzugriff (PDF)

The myeloproliferative disorder–associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3

Blood, 2007-06, Vol.109 (11), p.4924-4929

2007

Volltextzugriff (PDF)

The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels

Haematologica (Roma), 2007-12, Vol.92 (12), p.1607-1614

2007

Volltextzugriff (PDF)

Identification of high oxygen affinity hemoglobin variants in the investigation of patients with erythrocytosis

Haematologica (Roma), 2009-09, Vol.94 (9), p.1321-1322

2009

Volltextzugriff (PDF)

Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency

British journal of haematology, 2008-05, Vol.141 (3), p.298-308

2008

Volltextzugriff (PDF)

Erythrocytosis associated with a novel missense mutation in the HIF2A gene

Haematologica (Roma), 2010-05, Vol.95 (5), p.829-832

2010

Volltextzugriff (PDF)

Familial erythrocytosis: molecular links to red blood cell control

Haematologica (Roma), 2008-07, Vol.93 (7), p.963-967

2008

Volltextzugriff (PDF)

Tibetan PHD2, an allele with loss-of-function properties

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (22), p.12230-12238

2020

Volltextzugriff (PDF)

A Gain-of-Function Mutation in the HIF2A Gene in Familial Erythrocytosis

The New England journal of medicine, 2008-01, Vol.358 (2), p.162-168

2008

Volltextzugriff (PDF)

Potential prognostic marker ubiquitin carboxyl-terminal hydrolase-L1 does not predict patient survival in non-small cell lung carcinoma

Journal of experimental & clinical cancer research, 2011-08, Vol.30 (1), p.79-79, Article 79

2011

Volltextzugriff (PDF)

Regulation of human metabolism by hypoxia-inducible factor

Proceedings of the National Academy of Sciences - PNAS, 2010-07, Vol.107 (28), p.12722-12727

2010

Volltextzugriff (PDF)

A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1α (HIF-1α) does not impair Pro-564 hydroxylation

Molecular cancer, 2003-09, Vol.2 (1), p.31-31

2003

Volltextzugriff (PDF)

Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis

Blood, 2008-06, Vol.111 (11), p.5400-5402

2008

Volltextzugriff (PDF)

Polycythaemia‐inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor–EPOR chimeras

British journal of haematology, 2014-05, Vol.165 (4), p.519-528

2014

Volltextzugriff (PDF)

Oxygen Sensing: Recent Insights from Idiopathic Erythrocytosis

Cell cycle (Georgetown, Tex.), 2006-05, Vol.5 (9), p.941-945

2006

Volltextzugriff (PDF)

A novel splicing site IRP1 somatic mutation in a patient with pheochromocytoma and JAK2V617F positive polycythemia vera: a case report

BMC cancer, 2018-03, Vol.18 (1), p.286-286, Article 286

2018

Volltextzugriff (PDF)

Erythropoietin-induced activation of the JAK2/STAT5, PI3K/Akt, and Ras/ERK pathways promotes malignant cell behavior in a modified breast cancer cell line

Molecular cancer research, 2010-04, Vol.8 (4), p.615-626

2010

Volltextzugriff (PDF)

Erythrocytosis-associated HIF-2α Mutations Demonstrate a Critical Role for Residues C-terminal to the Hydroxylacceptor Proline

The Journal of biological chemistry, 2009-04, Vol.284 (14), p.9050-9058

2009

Volltextzugriff (PDF)

1 – 25 von 61

Suche als RSS-Feed

Aktive Filter

KollektionEZB Electronic Journals Library

PublikationsformArtikel

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(61)
Mit Volltextzugriff
(60)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(44)
Science & Technology
(40)
Life Sciences & Biomedicine
(37)
Hematology
(27)
Polycythemia - Genetics
(27)
Female
(21)
Mutation
(19)
Biological And Medical Sciences
(18)
Hematologic And Hematopoietic Diseases
(18)
Male
(18)
Medical Sciences
(18)
Adult
(15)
Diseases Of Red Blood Cells
(15)
Polycythemias
(12)
Basic Helix-Loop-Helix Transcription Factors - Genetics
(10)
Middle Aged
(10)
Polycythemia - Metabolism
(10)
Mutation, Missense
(9)
Erythropoietin
(8)
Amino Acid Substitution
(7)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(44)
Publisher website
(35)
Journals@Ovid Full Text
(18)
Wiley-Blackwell Journals
(14)
Wiley Online Library
(14)
Springer Journals
(6)
IngentaConnect Journals
(5)
Ingenta
(4)
Taylor & Francis Journals Complete
(3)
JSTOR
(3)
Taylor & Francis Journals Auto-Holdings Collection
(3)
Taylor & Francis
(3)
Nexis Uni
(1)
BMJ
(1)
BMJ Journals Archiv - DFG Nationallizenzen
(1)

10 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Erythrocytosis and Pulmonary Hypertension in a Mouse Model of Human HIF2A Gain of Function Mutation

Recessive congenital methaemoglobinaemia: cytochrome b5 reductase deficiency

A Family with Erythrocytosis Establishes a Role for Prolyl Hydroxylase Domain Protein 2 in Oxygen Homeostasis

A Knock-in Mouse Model of Human PHD2 Gene-associated Erythrocytosis Establishes a Haploinsufficiency Mechanism

A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove

Mutation of von Hippel-Lindau tumour suppressor and human cardiopulmonary physiology

The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms

The myeloproliferative disorder–associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3

The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels

Identification of high oxygen affinity hemoglobin variants in the investigation of patients with erythrocytosis

Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency

Erythrocytosis associated with a novel missense mutation in the HIF2A gene

Familial erythrocytosis: molecular links to red blood cell control

Tibetan PHD2, an allele with loss-of-function properties

A Gain-of-Function Mutation in the HIF2A Gene in Familial Erythrocytosis

Potential prognostic marker ubiquitin carboxyl-terminal hydrolase-L1 does not predict patient survival in non-small cell lung carcinoma

Hypoxia-inducible factor 2α regulates key neutrophil functions in humans, mice, and zebrafish

Regulation of human metabolism by hypoxia-inducible factor

A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1α (HIF-1α) does not impair Pro-564 hydroxylation

Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis

Polycythaemia‐inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor–EPOR chimeras

Oxygen Sensing: Recent Insights from Idiopathic Erythrocytosis

A novel splicing site IRP1 somatic mutation in a patient with pheochromocytoma and JAK2V617F positive polycythemia vera: a case report

Erythropoietin-induced activation of the JAK2/STAT5, PI3K/Akt, and Ras/ERK pathways promotes malignant cell behavior in a modified breast cancer cell line

Erythrocytosis-associated HIF-2α Mutations Demonstrate a Critical Role for Residues C-terminal to the Hydroxylacceptor Proline

Aktive Filter

Suchergebnisse filtern