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...

ETS1 mediates MEK1/2-dependent overexpression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancer cells

PloS one, 2011-03, Vol.6 (3), p.e17979

2011

Volltextzugriff (PDF)

Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis

Cogent medicine, 2019-01, Vol.6 (1), p.1582400

2019

Volltextzugriff (PDF)

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

BMB Reports, 2010, 43(8), , pp.530-534

2010

Volltextzugriff (PDF)

Why Crossmatch Tests are Very Important and What Do They Tell Us?

Turkish journal of nephrology, 2020-01, Vol.29 (1), p.77-81

2020

Volltextzugriff (PDF)

Comparison of Cytotoxic Flow Cytometric Cross Match With Complement Dependent Lymphocytotoxicity and Flow Cytometric Cross Match in Renal Transplant Patients

Transplantation proceedings, 2019-05, Vol.51 (4), p.1021-1023

2019

Volltextzugriff (PDF)

Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism

The journal of obstetrics and gynaecology research, 2008-02, Vol.34 (1), p.73-77

2008

Volltextzugriff (PDF)

Myxoma Virus Combination Therapy Enhances Lenalidomide and Bortezomib Treatments for Multiple Myeloma

Pathogens (Basel), 2024-01, Vol.13 (1), p.72

2024

Volltextzugriff (PDF)

Protective effects of Acetobacter ghanensis against gliadin toxicity in intestinal epithelial cells with immunoregulatory and gluten-digestive properties

European journal of nutrition, 2023-03, Vol.62 (2), p.605-614

2023

Volltextzugriff (PDF)

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

BMB reports, 2010-08, Vol.43 (8), p.530-534

2010

Volltextzugriff (PDF)

Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study

Medicine (Baltimore), 2022-08, Vol.101 (32), p.e29881-e29881

2022

Volltextzugriff (PDF)

First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population

Turkish journal of haematology, 2015-12, Vol.32 (4), p.374-375

2015

Volltextzugriff (PDF)

FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center

Gazi tıp dergisi, 2022-10, Vol.33 (4)

2022

Volltextzugriff (PDF)

First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population

Turkish journal of haematology, 2016-03, Vol.33 (1), p.71-72

2016

Volltextzugriff (PDF)

Prevalence and significance of the MEFV gene mutations in childhood Henoch–Schönlein purpura without FMF symptoms

Rheumatology international, 2013-02, Vol.33 (2), p.377-380

2013

Volltextzugriff (PDF)

Chk1 Targeting Reactivates PP2A Tumor Suppressor Activity in Cancer Cells

Cancer research (Chicago, Ill.), 2013-11, Vol.73 (22), p.6757-6769

2013

Volltextzugriff (PDF)

A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C

Hemoglobin, 2016-07, Vol.40 (4), p.280-282

2016

Volltextzugriff (PDF)

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya

Turkish journal of haematology, 2016-06, Vol.33 (2), p.107-111

2016

Volltextzugriff (PDF)

788: The association between inherited thrombophilias and pregnancy-related hypertension recurrence

American journal of obstetrics and gynecology, 2009-12, Vol.201 (6), p.S283-S283

2009

Volltextzugriff (PDF)

The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population

Blood cells, molecules, & diseases, 2011-03, Vol.46 (3), p.226-229

2011

Volltextzugriff (PDF)

ETS1 Mediates MEK1/2-Dependent Overexpression of Cancerous Inhibitor of Protein Phosphatase 2A

PloS one, 2011-03, Vol.6 (3), p.e17979

2011

Volltextzugriff (PDF)

Investigation of the Effects of Piperlongumine and Doxorubicin Combined Treatment on Cell Death via PTEN in HeLa Cells

Yüzüncü Yıl Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2024-04, Vol.29 (1), p.1-11

2024

Volltextzugriff (PDF)

The association between inherited thrombophilias and pregnancy-related hypertension recurrence

Archives of gynecology and obstetrics, 2011-10, Vol.284 (4), p.837-841

2011

Volltextzugriff (PDF)

Alloreactive memory B cell detection by flow cytometric cross match using polyclonally activated memory B cell culture supernatants

Transplant immunology, 2022-08, Vol.73, p.101642-101642, Article 101642

2022

Volltextzugriff (PDF)

Complement Factor H Y403H Polymorphism in the Turkish Population

Balkan journal of medical genetics, 2010-01, Vol.13 (2), p.41-45

2010

Volltextzugriff (PDF)

The effect of HBB: c.+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype

Turkish journal of haematology, 2011-09, Vol.28 (3), p.219-222

2011

Volltextzugriff (PDF)

1 – 25 von 48

Suche als RSS-Feed

Aktive Filter

KollektionOxford Journals 2020 Medicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(43)

Publikationsform

Artikel
(48)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(23)
Life Sciences & Biomedicine
(22)
Humans
(19)
Female
(12)
Male
(9)
Middle Aged
(7)
Mutation
(7)
Turkey
(6)
Adult
(4)
Beta-Globins - Genetics
(4)
Hematology
(4)
Medicine
(4)
Polymorphism, Genetic
(4)
Turkish Population
(4)
Alleles
(3)
Beta-Thalassemia - Genetics
(3)
Case-Control Studies
(3)
European Continental Ancestry Group - Genetics
(3)
Gene Frequency
(3)
General & Internal Medicine
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

ETS1 mediates MEK1/2-dependent overexpression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancer cells

Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

Why Crossmatch Tests are Very Important and What Do They Tell Us?

Comparison of Cytotoxic Flow Cytometric Cross Match With Complement Dependent Lymphocytotoxicity and Flow Cytometric Cross Match in Renal Transplant Patients

Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism

Myxoma Virus Combination Therapy Enhances Lenalidomide and Bortezomib Treatments for Multiple Myeloma

Protective effects of Acetobacter ghanensis against gliadin toxicity in intestinal epithelial cells with immunoregulatory and gluten-digestive properties

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study

First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population

FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center

First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population

Prevalence and significance of the MEFV gene mutations in childhood Henoch–Schönlein purpura without FMF symptoms

Chk1 Targeting Reactivates PP2A Tumor Suppressor Activity in Cancer Cells

A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya

788: The association between inherited thrombophilias and pregnancy-related hypertension recurrence

The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population

ETS1 Mediates MEK1/2-Dependent Overexpression of Cancerous Inhibitor of Protein Phosphatase 2A

Investigation of the Effects of Piperlongumine and Doxorubicin Combined Treatment on Cell Death via PTEN in HeLa Cells

The association between inherited thrombophilias and pregnancy-related hypertension recurrence

Alloreactive memory B cell detection by flow cytometric cross match using polyclonally activated memory B cell culture supernatants

Complement Factor H Y403H Polymorphism in the Turkish Population

The effect of HBB: c.+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype

Aktive Filter

Suchergebnisse filtern