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...

Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study

The lancet oncology, 2022-01, Vol.23 (1), p.161-171

2022

Volltextzugriff (PDF)

E‐health education interventions on HbA1c in patients with type 1 diabetes on intensive insulin therapy: A systematic review and meta‐analysis of randomized controlled trials

Diabetes/metabolism research and reviews, 2020-09, Vol.36 (6), p.e3313-n/a

2020

Volltextzugriff (PDF)

A noncoding RNA modulator potentiates phenylalanine metabolism in mice

Science (American Association for the Advancement of Science), 2021-08, Vol.373 (6555), p.662-673

2021

Volltextzugriff (PDF)

Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis

Nature communications, 2023-01, Vol.14 (1), p.309-309, Article 309

2023

Volltextzugriff (PDF)

The Fate of Transplanted Olfactory Progenitors Is Conditioned by the Cell Phenotypes of the Receiver Brain Tissue in Cocultures

International journal of molecular sciences, 2020-10, Vol.21 (19), p.7249

2020

Volltextzugriff (PDF)

Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome

Genetics in medicine, 2019-09, Vol.21 (9), p.2025-2035

2019

Volltextzugriff (PDF)

HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotyping

Journal of allergy and clinical immunology, 2015-01, Vol.135 (1), p.253-259.e10

2015

Volltextzugriff (PDF)

Vitamin B12 Deficiency Dysregulates m6A mRNA Methylation of Genes Involved in Neurological Functions

Molecular nutrition & food research, 2021-09, Vol.65 (17), p.e2100206-n/a

2021

Volltextzugriff (PDF)

Elastase and exacerbation of neutrophil innate immunity are involved in multi‐visceral manifestations of COVID‐19

Allergy (Copenhagen), 2021-06, Vol.76 (6), p.1846-1858

2021

Volltextzugriff (PDF)

Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations

The American journal of clinical nutrition, 2006-03, Vol.83 (3), p.701-707

2006

Volltextzugriff (PDF)

The importance of gene-environment interactions in human obesity

Clinical science (1979), 2016-09, Vol.130 (18), p.1571-1597

2016

Volltextzugriff (PDF)

Glucocorticoid Receptor Activation Restores Learning Memory by Modulating Hippocampal Plasticity in a Mouse Model of Brain Vitamin B12 Deficiency

Molecular neurobiology, 2021-03, Vol.58 (3), p.1024-1035

2021

Volltextzugriff (PDF)

Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency

Biochimie, 2016-07, Vol.126, p.43-51

2016

Volltextzugriff (PDF)

Mechanisms of homocysteine-induced damage to the endothelial, medial and adventitial layers of the arterial wall

Biochimie, 2020-06, Vol.173, p.100-106

2020

Volltextzugriff (PDF)

Proof of concept and development of a couple-based machine learning model to stratify infertile patients with idiopathic infertility

Scientific reports, 2021-12, Vol.11 (1), p.24003-24003, Article 24003

2021

Volltextzugriff (PDF)

Next‐generation sequencing and genotype association studies reveal the association of HLA‐DRB302:02 with delayed hypersensitivity to penicillins

Allergy (Copenhagen), 2022-06, Vol.77 (6), p.1827-1834

2022

Volltextzugriff (PDF)

Blood myeloperoxidase‐DNA, a biomarker of early response to SARS‐CoV‐2 infection?

Allergy (Copenhagen), 2021-03, Vol.76 (3), p.892-896

2021

Volltextzugriff (PDF)

Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cells development and retinal metabolism

Clinical epigenetics, 2024-02, Vol.16 (1), p.23-23, Article 23

2024

Volltextzugriff (PDF)

Folate and fetal programming: a play in epigenomics?

Trends in endocrinology and metabolism, 2013-06, Vol.24 (6), p.279-289

2013

Volltextzugriff (PDF)

Health outcomes associated with vegetarian diets: An umbrella review of systematic reviews and meta-analyses

Clinical nutrition (Edinburgh, Scotland), 2020-11, Vol.39 (11), p.3283-3307

2020

Volltextzugriff (PDF)

1 – 25 von 421

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(391)
Mit Volltextzugriff
(369)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(293)
Life Sciences & Biomedicine
(278)
Humans
(210)
Female
(136)
Life Sciences
(133)
Male
(108)
Biological And Medical Sciences
(95)
Animals
(80)
Adult
(69)
Medical Sciences
(66)
Middle Aged
(65)
Vitamin B12
(56)
Biochemistry & Molecular Biology
(53)
Homocysteine
(51)
Rats
(42)
Vitamin B
(42)
Folate
(40)
Aged
(38)
Fundamental And Applied Biological Sciences. Psychology
(37)
Gastroenterology & Hepatology
(34)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study

E‐health education interventions on HbA1c in patients with type 1 diabetes on intensive insulin therapy: A systematic review and meta‐analysis of randomized controlled trials

Plasma mSEPT9: A Novel Circulating Cell-free DNA-Based Epigenetic Biomarker to Diagnose Hepatocellular Carcinoma

A noncoding RNA modulator potentiates phenylalanine metabolism in mice

Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis

The Fate of Transplanted Olfactory Progenitors Is Conditioned by the Cell Phenotypes of the Receiver Brain Tissue in Cocultures

Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome

HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotyping

Vitamin B12 Deficiency Dysregulates m6A mRNA Methylation of Genes Involved in Neurological Functions

Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia

Elastase and exacerbation of neutrophil innate immunity are involved in multi‐visceral manifestations of COVID‐19

WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation

Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations

The importance of gene-environment interactions in human obesity

Glucocorticoid Receptor Activation Restores Learning Memory by Modulating Hippocampal Plasticity in a Mouse Model of Brain Vitamin B12 Deficiency

Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency

Mechanisms of homocysteine-induced damage to the endothelial, medial and adventitial layers of the arterial wall

Proof of concept and development of a couple-based machine learning model to stratify infertile patients with idiopathic infertility

Next‐generation sequencing and genotype association studies reveal the association of HLA‐DRB302:02 with delayed hypersensitivity to penicillins

Blood myeloperoxidase‐DNA, a biomarker of early response to SARS‐CoV‐2 infection?

Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cells development and retinal metabolism

Folate and fetal programming: a play in epigenomics?

The spectrum of biochemical alterations associated with organ dysfunction and inflammatory status and their association with disease outcomes in severe COVID-19: A longitudinal cohort and time-series design study

Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs

Health outcomes associated with vegetarian diets: An umbrella review of systematic reviews and meta-analyses

Suchergebnisse filtern