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...

Fibroblast growth factor 21 attenuates ventilator-induced lung injury by inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway

Critical care (London, England), 2023-05, Vol.27 (1), p.196-196, Article 196

2023

Volltextzugriff (PDF)

ILK–PI3K/AKT pathway participates in cutaneous wound contraction by regulating fibroblast migration and differentiation to myofibroblast

Laboratory investigation, 2016-07, Vol.96 (7), p.741-751

2016

Volltextzugriff (PDF)

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent

PloS one, 2015-07, Vol.10 (7), p.e0132034-e0132034

2015

Volltextzugriff (PDF)

Seroprevalence of Human Immunodeficiency Virus, Hepatitis B Virus, Hepatitis C Virus, and Treponema pallidum Infections among Blood Donors on Bioko Island, Equatorial Guinea

PloS one, 2015-10, Vol.10 (10), p.e0139947-e0139947

2015

Volltextzugriff (PDF)

UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China

BMC pediatrics, 2021-06, Vol.21 (1), p.259-259, Article 259

2021

Volltextzugriff (PDF)

Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China

PloS one, 2014-07, Vol.9 (7), p.e101505-e101505

2014

Volltextzugriff (PDF)

Molecular epidemiological investigation of abnormal hemoglobin in Shaokwan region, southern China

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.150-156

2022

Volltextzugriff (PDF)

Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

BMC pediatrics, 2021-12, Vol.21 (1), p.564-564, Article 564

2021

Volltextzugriff (PDF)

Clinical validation of a single-tube PCR and reverse dot blot assay for detection of common α-thalassaemia and β-thalassaemia in Chinese

Journal of international medical research, 2022-02, Vol.50 (2), p.3000605221078785-3000605221078785

2022

Volltextzugriff (PDF)

Human serum albumin variants in China: a molecular epidemiological investigation and literature review

Journal of international medical research, 2021-12, Vol.49 (12), p.3000605211064225-3000605211064225

2021

Volltextzugriff (PDF)

Glucose-6-phosphate dehydrogenase deficiency screening and gene analysis in blood donors of Guangdong province

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.494-498

2022

Volltextzugriff (PDF)

Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China

PloS one, 2013-02, Vol.8 (2), p.e55024-e55024

2013

Volltextzugriff (PDF)

Epidemiologic characterization of human papillomavirus infection in rural Chaozhou, eastern Guangdong Province of China

PloS one, 2012-02, Vol.7 (2), p.e32149-e32149

2012

Volltextzugriff (PDF)

High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population

PloS one, 2014-08, Vol.9 (8), p.e102243-e102243

2014

Volltextzugriff (PDF)

Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia

Pediatrics and neonatology, 2016-08, Vol.57 (4), p.310-317

2016

Volltextzugriff (PDF)

The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China

Gene, 2018-12, Vol.678, p.312-317

2018

Volltextzugriff (PDF)

Hospitalized children with COVID-19 infection during large outbreak of SARS-CoV-2 Omicron strain: a retrospective study in Chaozhou, Guangdong, China

Annals of medicine (Helsinki), 2024-12, Vol.56 (1), p.2389301

2024

Volltextzugriff (PDF)

Reconstructing a Full-Thickness Cheek Defect of Electrical Burn With a Folding Radial Forearm Flap

Journal of oral and maxillofacial surgery, 2013-10, Vol.71 (10), p.1811.e1-1811.e3

2013

Volltextzugriff (PDF)

Human umbilical cord Wharton's Jelly-derived mesenchymal stem cells differentiation into nerve-like cells

Chinese medical journal, 2005-12, Vol.118 (23), p.1987-1993

2005

Volltextzugriff (PDF)

Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia

Neonatology (Basel, Switzerland), 2023-07, Vol.120 (3), p.371-380

2023

Volltextzugriff (PDF)

Genotype and phenotype analysis of α-thalassemia fusion gene in southern China

Hematology (Luxembourg), 2024-12, Vol.29 (1), p.2399361

2024

Volltextzugriff (PDF)

Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification

Blood coagulation & fibrinolysis, 2020-03, Vol.31 (2), p.160-164

2020

Volltextzugriff (PDF)

Fibroblast growth factor 10 protects neuron against oxygen–glucose deprivation injury through inducing heme oxygenase-1

Biochemical and biophysical research communications, 2015-01, Vol.456 (1), p.225-231

2015

Volltextzugriff (PDF)

Genital human papillomavirus screening by gene chip in Chinese women of Guangdong province

Australian & New Zealand journal of obstetrics & gynaecology, 2008-04, Vol.48 (2), p.189-194

2008

Volltextzugriff (PDF)

Hepatitis B virus infection and replication in primarily cultured human fetal hepatocytes

World journal of gastroenterology : WJG, 2007-02, Vol.13 (7), p.1027

2007

Volltextzugriff (PDF)

1 – 25 von 426

Suche als RSS-Feed

Aktive Filter

ThemaChemistry

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(336)
Mit Volltextzugriff
(345)

Publikationsform

Artikel
(425)
Tagungsberichte
(1)

Sprache

Englisch
(369)
Chinesisch
(58)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(11)

Menü

Weitere Dienste

Einstellungen

Fibroblast growth factor 21 attenuates ventilator-induced lung injury by inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway

ILK–PI3K/AKT pathway participates in cutaneous wound contraction by regulating fibroblast migration and differentiation to myofibroblast

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent

Seroprevalence of Human Immunodeficiency Virus, Hepatitis B Virus, Hepatitis C Virus, and Treponema pallidum Infections among Blood Donors on Bioko Island, Equatorial Guinea

UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China

Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China

Molecular epidemiological investigation of abnormal hemoglobin in Shaokwan region, southern China

Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

Clinical validation of a single-tube PCR and reverse dot blot assay for detection of common α-thalassaemia and β-thalassaemia in Chinese

Human serum albumin variants in China: a molecular epidemiological investigation and literature review

Glucose-6-phosphate dehydrogenase deficiency screening and gene analysis in blood donors of Guangdong province

Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China

Epidemiologic characterization of human papillomavirus infection in rural Chaozhou, eastern Guangdong Province of China

High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population

Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia

The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China

Hospitalized children with COVID-19 infection during large outbreak of SARS-CoV-2 Omicron strain: a retrospective study in Chaozhou, Guangdong, China

Reconstructing a Full-Thickness Cheek Defect of Electrical Burn With a Folding Radial Forearm Flap

Human umbilical cord Wharton's Jelly-derived mesenchymal stem cells differentiation into nerve-like cells

Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia

Genotype and phenotype analysis of α-thalassemia fusion gene in southern China

Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification

Fibroblast growth factor 10 protects neuron against oxygen–glucose deprivation injury through inducing heme oxygenase-1

Genital human papillomavirus screening by gene chip in Chinese women of Guangdong province

Hepatitis B virus infection and replication in primarily cultured human fetal hepatocytes

Aktive Filter

Suchergebnisse filtern