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...

Effect of Decorin and Dermatan Sulfate on the Mechanical Properties of a Neocartilage

Connective tissue research, 2010-04, Vol.51 (2), p.159-170

2010

Volltextzugriff (PDF)

A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals

Mechanisms of ageing and development, 2011-06, Vol.132 (6), p.324-330

2011

Volltextzugriff (PDF)

comprehensive evaluation of SNP genotype imputation

Human genetics, 2009-03, Vol.125 (2), p.163-171

2009

Volltextzugriff (PDF)

Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice

Gastroenterology (New York, N.Y. 1943), 2017-08, Vol.153 (2), p.550-565

2017

Volltextzugriff (PDF)

Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies

Gastroenterology (New York, N.Y. 1943), 2013-08, Vol.145 (2), p.339-347

2013

Volltextzugriff (PDF)

Human growth hormone 1 (GH1) gene expression: Complex haplotype‐dependent influence of polymorphic variation in the proximal promoter and locus control region

Human mutation, 2003-04, Vol.21 (4), p.408-423

2003

Volltextzugriff (PDF)

Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature

Human mutation, 2003-04, Vol.21 (4), p.424-440

2003

Volltextzugriff (PDF)

Growth hormone ( GH1) gene variation and the growth hormone receptor ( GHR) exon 3 deletion polymorphism in a West-African population

Molecular and cellular endocrinology, 2008-12, Vol.296 (1), p.18-25

2008

Volltextzugriff (PDF)

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2

Cold Spring Harbor molecular case studies, 2019-02, Vol.5 (1), p.a002428

2019

Volltextzugriff (PDF)

How to distinguish genetically between an alleged father and his monozygotic twin: A thought experiment

Forensic science international : genetics, 2012-09, Vol.6 (5), p.e129-e130

2012

Volltextzugriff (PDF)

Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke

Human genetics, 2006-06, Vol.119 (5), p.527-540

2006

Volltextzugriff (PDF)

Location of mutations within the PKD2 gene influences clinical outcome

Kidney international, 2000-04, Vol.57 (4), p.1444-1451

2000

Volltextzugriff (PDF)

Molecular analysis of the genotype-phenotype relationship in factor X deficiency

Human genetics, 2000-02, Vol.106 (2), p.249-257

2000

Volltextzugriff (PDF)

Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1

Human genetics, 2003, Vol.112 (1), p.12-17

2003

Volltextzugriff (PDF)

Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selection

Human mutation, 1995, Vol.5 (1), p.48-57

1995

Volltextzugriff (PDF)

Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiency

Journal of medical genetics, 1995-07, Vol.32 (7), p.543-545

1995

Volltextzugriff (PDF)

Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNA

Human genetics, 1998-08, Vol.103 (2), p.228-233

1998

Volltextzugriff (PDF)

RNA-binding proteins and human male infertility

Trends in genetics, 1997-03, Vol.13 (3), p.87-89

1997

Volltextzugriff (PDF)

Discrimination between recurrent mutation and identity by descent : application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene

Human genetics, 1991-08, Vol.87 (4), p.457-461

1991

Volltextzugriff (PDF)

1 – 20 von 20

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(20)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(20)

Sprache

Englisch
(20)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(20)
Science & Technology
(20)
Humans
(19)
Female
(14)
Genetics & Heredity
(13)
Biological And Medical Sciences
(11)
Medical Sciences
(8)
Fundamental And Applied Biological Sciences. Psychology
(6)
Genotype
(6)
Genetic Variation
(5)
Polymorphism, Single Nucleotide
(5)
Adult
(4)
Animals
(4)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(4)
Haplotypes
(4)
Mutation, Missense
(4)
Alleles
(3)
Base Sequence
(3)
Case-Control Studies
(3)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Effect of Decorin and Dermatan Sulfate on the Mechanical Properties of a Neocartilage

A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals

comprehensive evaluation of SNP genotype imputation

Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice

Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies

Human growth hormone 1 (GH1) gene expression: Complex haplotype‐dependent influence of polymorphic variation in the proximal promoter and locus control region

Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature

Growth hormone ( GH1) gene variation and the growth hormone receptor ( GHR) exon 3 deletion polymorphism in a West-African population

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2

How to distinguish genetically between an alleged father and his monozygotic twin: A thought experiment

Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke

Location of mutations within the PKD2 gene influences clinical outcome

Molecular analysis of the genotype-phenotype relationship in factor X deficiency

Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1

Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selection

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population

Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiency

Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNA

RNA-binding proteins and human male infertility

Discrimination between recurrent mutation and identity by descent : application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene

Aktive Filter

Suchergebnisse filtern