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...

Defining screening panel of functional variants of CYP1A1, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 genes in Serbian population

International journal of legal medicine, 2020-03, Vol.134 (2), p.433-439

2020

Volltextzugriff (PDF)

Cryptic Diversity of the European Blind Mole Rat Nannospalax leucodon Species Complex: Implications for Conservation

Animals (Basel), 2022-04, Vol.12 (9), p.1097

2022

Volltextzugriff (PDF)

Transgenerational Sub-Lethal Pyrethroid Exposure Affects Shape Variation and Fluctuating Asymmetry in Seed Beetles

Symmetry (Basel), 2024-08, Vol.16 (8), p.995

2024

Volltextzugriff (PDF)

Vitamin D Serum Levels and Vitamin D Receptor Genotype in Patients with Parkinson’s Disease

Neuroscience, 2023-11, Vol.533, p.53-62

2023

Volltextzugriff (PDF)

A Cryptic Subterranean Mammal Species, the Lesser Blind Mole Rat ( Nannospalax leucodon syrmiensis )-Retreated but Not Extinct

Animals (Basel), 2024-02, Vol.14 (5), p.774

2024

Volltextzugriff (PDF)

The angiotensin converting enzyme (ace) gene polymorphism: Insight study of the renal regulation of the arterial blood pressure

Medicinski podmladak, 2016, Vol.67 (3), p.31-35

2016

Volltextzugriff (PDF)

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

Nature (London), 2007-08, Vol.448 (7157), p.1058-1062

2007

Volltextzugriff (PDF)

Case Report: Post-mortem Histopathological and Molecular Analyses of the Very First Documented COVID-19-Related Death in Europe

Frontiers in medicine, 2021-02, Vol.8, p.612758

2021

Volltextzugriff (PDF)

Prediction of autosomal STR typing success in ancient and Second World War bone samples

Forensic science international : genetics, 2017-03, Vol.27, p.17-26

2017

Volltextzugriff (PDF)

16S rRNA gene polymorphism supports cryptic speciation within the lesser blind mole rat Nannospalax leucodon superspecies (Rodentia: Spalacidae)

Mammalian biology : Zeitschrift für Säugetierkunde, 2020-06, Vol.100 (3), p.315-324

2020

Volltextzugriff (PDF)

Polymorphisms in ACE and ACTN3 Genes and Blood Pressure Response to Acute Exercise in Elite Male Athletes from Serbia

The Tohoku Journal of Experimental Medicine, 2017, Vol.243(4), pp.311-320

2017

Volltextzugriff (PDF)

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation

Scientific reports, 2016-02, Vol.6 (1), p.20369-20369, Article 20369

2016

Volltextzugriff (PDF)

Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertility

Blood coagulation & fibrinolysis, 2021-03, Vol.32 (2), p.103-107

2021

Volltextzugriff (PDF)

Y-STR profiling in two Afghanistan populations

Legal medicine (Tokyo, Japan), 2011-03, Vol.13 (2), p.103-108

2011

Volltextzugriff (PDF)

Principal components analysis to evaluate complex association of polymorphisms in ACE and ACTN3 genes and the extent of cardiovascular adaptive changes in elite athletes

Journal of sports medicine and physical fitness, 2024-02, Vol.64 (2), p.192

2024

Volltextzugriff (PDF)

Forensic DNA databases in Western Balkan region: retrospectives, perspectives, and initiatives

Croatian medical journal, 2011-06, Vol.52 (3), p.235-244

2011

Volltextzugriff (PDF)

Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertility

Human fertility (Cambridge, England), 2020-04, Vol.23 (2), p.101-110

2020

Volltextzugriff (PDF)

Hemostasis-related gene polymorphisms and their epistatic relationship in women with idiopathic infertility

Blood coagulation & fibrinolysis, 2019-09, Vol.30 (6), p.253-262

2019

Volltextzugriff (PDF)

POOR GRAFT FUNCTION - CAUSES AND POTENTIAL SOLUTIONS/SLABOST KALEMA - UZROCI I POTENCIJALNA RESENJA

Medicinski pregled, 2022-10, Vol.75 (S1), p.45

2022

Volltextzugriff (PDF)

Poor graft function - causes and potential solutions

Medicinski pregled, 2022, Vol.75 (Suppl. 1), p.45-49

2022

Volltextzugriff (PDF)

250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1

Human mutation, 2002-02, Vol.19 (2), p.131-139

2002

Volltextzugriff (PDF)

Influence of ACE and ACTN3 genes polymorphisms on cardiovascular adaptation in female football players

Genetika (Beograd), 2022, Vol.54 (3), p.1035-1047

2022

Volltextzugriff (PDF)

O-23 ACE and ACTN3 genes polymorphisms among elite male serbian athletes

British journal of sports medicine, 2016-11, Vol.50 (Suppl 1), p.A12-A13

2016

Volltextzugriff (PDF)

On the Bantu expansion

Gene, 2016-11, Vol.593 (1), p.48-57

2016

Volltextzugriff (PDF)

Corrigendum to “On the Bantu expansion” [GENE 593/1 (2016) 48–57]

Gene, 2017-02, Vol.602, p.57-57

2017

Volltextzugriff (PDF)

1 – 25 von 52

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(43)

Publikationsform

Artikel
(51)
Berichte
(1)

Sprache

Englisch
(52)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Defining screening panel of functional variants of CYP1A1, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 genes in Serbian population

Cryptic Diversity of the European Blind Mole Rat Nannospalax leucodon Species Complex: Implications for Conservation

Transgenerational Sub-Lethal Pyrethroid Exposure Affects Shape Variation and Fluctuating Asymmetry in Seed Beetles

Vitamin D Serum Levels and Vitamin D Receptor Genotype in Patients with Parkinson’s Disease

A Cryptic Subterranean Mammal Species, the Lesser Blind Mole Rat ( Nannospalax leucodon syrmiensis )-Retreated but Not Extinct

The angiotensin converting enzyme (ace) gene polymorphism: Insight study of the renal regulation of the arterial blood pressure

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

Case Report: Post-mortem Histopathological and Molecular Analyses of the Very First Documented COVID-19-Related Death in Europe

Prediction of autosomal STR typing success in ancient and Second World War bone samples

16S rRNA gene polymorphism supports cryptic speciation within the lesser blind mole rat Nannospalax leucodon superspecies (Rodentia: Spalacidae)

Polymorphisms in ACE and ACTN3 Genes and Blood Pressure Response to Acute Exercise in Elite Male Athletes from Serbia

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation

Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertility

Y-STR profiling in two Afghanistan populations

Principal components analysis to evaluate complex association of polymorphisms in ACE and ACTN3 genes and the extent of cardiovascular adaptive changes in elite athletes

Forensic DNA databases in Western Balkan region: retrospectives, perspectives, and initiatives

Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertility

Hemostasis-related gene polymorphisms and their epistatic relationship in women with idiopathic infertility

POOR GRAFT FUNCTION - CAUSES AND POTENTIAL SOLUTIONS/SLABOST KALEMA - UZROCI I POTENCIJALNA RESENJA

Poor graft function - causes and potential solutions

250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1

Influence of ACE and ACTN3 genes polymorphisms on cardiovascular adaptation in female football players

O-23 ACE and ACTN3 genes polymorphisms among elite male serbian athletes

On the Bantu expansion

Corrigendum to “On the Bantu expansion” [GENE 593/1 (2016) 48–57]

Suchergebnisse filtern