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...

The basis of mink susceptibility to SARS-CoV-2 infection

Journal of applied genetics, 2022-09, Vol.63 (3), p.543-555

2022

Volltextzugriff (PDF)

Circulating miRNA as potential biomarkers for diabetes mellitus type 2: should we focus on searching for sex differences?

Journal of applied genetics, 2022-05, Vol.63 (2), p.293-303

2022

Volltextzugriff (PDF)

In-silico analysis of Thr767Ile pathogenic variant in the MSH6 gene in family with endometrial cancer

European journal of obstetrics & gynecology and reproductive biology, 2019-07, Vol.238, p.54-57

2019

Volltextzugriff (PDF)

Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease - A Systematic Review

Frontiers in immunology, 2021-12, Vol.12, p.790803

2021

Volltextzugriff (PDF)

Physical Activity and DNA Methylation in Humans

International journal of molecular sciences, 2021-12, Vol.22 (23), p.12989

2021

Volltextzugriff (PDF)

Low-Penetrance Susceptibility Variants in Colorectal Cancer-Current Outlook in the Field

International journal of molecular sciences, 2024-08, Vol.25 (15), p.8338

2024

Volltextzugriff (PDF)

Role of rs2366152 single-nucleotide variant located in the long noncoding RNA HOTAIR gene in the cervical cancer susceptibility in a Polish population

Journal of applied genetics, 2024-09, Vol.65 (3), p.511-518

2024

Volltextzugriff (PDF)

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

Journal of applied genetics, 2021-05, Vol.62 (2), p.327-337

2021

Volltextzugriff (PDF)

Colorectal carcinoma in the course of inflammatory bowel diseases

Hereditary cancer in clinical practice, 2019-07, Vol.17 (1), p.18-9, Article 18

2019

Volltextzugriff (PDF)

NTHL1 Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14548

2023

Volltextzugriff (PDF)

The prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP

International journal of colorectal disease, 2011-09, Vol.26 (9), p.1197-1203

2011

Volltextzugriff (PDF)

Modern therapies of nonsmall cell lung cancer

Journal of applied genetics, 2023-12, Vol.64 (4), p.695-711

2023

Volltextzugriff (PDF)

The Regulation of Collagen Processing by miRNAs in Disease and Possible Implications for Bone Turnover

International journal of molecular sciences, 2021-12, Vol.23 (1), p.91

2021

Volltextzugriff (PDF)

In silico and in vitro analysis of the impact of single substitutions within EXO-motifs on Hsa-MiR-1246 intercellular transfer in breast cancer cell

Journal of applied genetics, 2023-02, Vol.64 (1), p.105-124

2023

Volltextzugriff (PDF)

Endoscopic Surveillance and Treatment of Upper GI Tract Lesions in Patients with Familial Adenomatous Polyposis-A New Perspective on an Old Disease

Genes, 2022-12, Vol.13 (12), p.2329

2022

Volltextzugriff (PDF)

Mutations in Helicobacter pylori infected patients with chronic gastritis, intestinal type of gastric cancer and familial gastric cancer

Hereditary cancer in clinical practice, 2024-06, Vol.22 (1), p.9-11

2024

Volltextzugriff (PDF)

Genetic variants of MTHFR gene in relation to folic acid levels and bone mineral density in Polish patients with inflammatory bowel disease

Journal of applied genetics, 2024-02, Vol.65 (1), p.73-81

2024

Volltextzugriff (PDF)

Strong Hereditary Predispositions to Colorectal Cancer

Genes, 2022-12, Vol.13 (12), p.2326

2022

Volltextzugriff (PDF)

No dynamic changes in the expression of genes related to the epigenetic mechanism during acute exercise

Journal of applied genetics, 2023-02, Vol.64 (1), p.81-87

2023

Volltextzugriff (PDF)

Polymorphic variants in genes related to stress coping are associated with the awake bruxism

BMC oral health, 2021-10, Vol.21 (1), p.496-496, Article 496

2021

Volltextzugriff (PDF)

Absence of the RET+3:T allele in the MTC patients

Hereditary cancer in clinical practice, 2012-10, Vol.10 (1), p.14-14, Article 14

2012

Volltextzugriff (PDF)

Novel genetic variants potentially associated with the pathogenesis of coronary artery aneurysm: whole-exome sequencing analysis

Hellenic journal of cardiology, 2024-09, Vol.79, p.84-85

2024

Volltextzugriff (PDF)

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

Hereditary cancer in clinical practice, 2012-12, Vol.10 (Suppl 4), p.A11-A11

2012

Volltextzugriff (PDF)

Crohn’s Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes

Journal of clinical medicine, 2021-08, Vol.10 (17), p.3777

2021

Volltextzugriff (PDF)

Colorectal cancer in the course of familial adenomatous polyposis syndrome ("de novo" pathogenic mutation of APC gene): case report, review of the literature and genetic commentary

Archives of medical science, 2010-04, Vol.6 (2), p.283-287

2010

Volltextzugriff (PDF)

1 – 25 von 79

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(74)
Mit Volltextzugriff
(74)

Publikationsform

Artikel
(76)
Berichte
(3)

Sprache

Englisch
(77)
Polnisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(57)
Life Sciences & Biomedicine
(56)
Humans
(35)
Mutation
(25)
Female
(19)
Genetics & Heredity
(18)
Oncology
(18)
Genes
(16)
Biomedical And Life Sciences
(14)
Human Genetics
(14)
Genetic Aspects
(13)
Biotechnology & Applied Microbiology
(11)
Health Aspects
(11)
Male
(11)
Animal Genetics And Genomics
(10)
Colorectal Cancer
(10)
Life Sciences
(10)
Microbial Genetics And Genomics
(10)
Plant Genetics And Genomics
(10)
Risk Factors
(9)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

The basis of mink susceptibility to SARS-CoV-2 infection

Circulating miRNA as potential biomarkers for diabetes mellitus type 2: should we focus on searching for sex differences?

In-silico analysis of Thr767Ile pathogenic variant in the MSH6 gene in family with endometrial cancer

Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease - A Systematic Review

Physical Activity and DNA Methylation in Humans

Low-Penetrance Susceptibility Variants in Colorectal Cancer-Current Outlook in the Field

Role of rs2366152 single-nucleotide variant located in the long noncoding RNA HOTAIR gene in the cervical cancer susceptibility in a Polish population

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

Colorectal carcinoma in the course of inflammatory bowel diseases

NTHL1 Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

The prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP

Modern therapies of nonsmall cell lung cancer

The Regulation of Collagen Processing by miRNAs in Disease and Possible Implications for Bone Turnover

In silico and in vitro analysis of the impact of single substitutions within EXO-motifs on Hsa-MiR-1246 intercellular transfer in breast cancer cell

Endoscopic Surveillance and Treatment of Upper GI Tract Lesions in Patients with Familial Adenomatous Polyposis-A New Perspective on an Old Disease

Mutations in Helicobacter pylori infected patients with chronic gastritis, intestinal type of gastric cancer and familial gastric cancer

Genetic variants of MTHFR gene in relation to folic acid levels and bone mineral density in Polish patients with inflammatory bowel disease

Strong Hereditary Predispositions to Colorectal Cancer

No dynamic changes in the expression of genes related to the epigenetic mechanism during acute exercise

Polymorphic variants in genes related to stress coping are associated with the awake bruxism

Absence of the RET+3:T allele in the MTC patients

Novel genetic variants potentially associated with the pathogenesis of coronary artery aneurysm: whole-exome sequencing analysis

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

Crohn’s Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes

Colorectal cancer in the course of familial adenomatous polyposis syndrome ("de novo" pathogenic mutation of APC gene): case report, review of the literature and genetic commentary

Suchergebnisse filtern