UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 93

Sortiert nach

A Method to Cleave Target Molecules in a Neocartilage

Connective tissue research, 2012-10, Vol.53 (5), p.430-436

2012

Volltextzugriff (PDF)

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)

Influence of bone morphogenetic protein-2 on the extracellular matrix, material properties, and gene expression of long-term articular chondrocyte cultures: loss of chondrocyte stability

Tissue engineering. Part A, 2009-06, Vol.15 (6), p.1247

2009

Volltextzugriff (PDF)

Collagen 11a1 is indirectly activated by lymphocyte enhancer-binding factor 1 (Lef1) and negatively regulates osteoblast maturation

Matrix biology, 2008-05, Vol.27 (4), p.330-338

2008

Volltextzugriff (PDF)

Effect of dermatan sulfate on the indentation and tensile properties of articular cartilage

Osteoarthritis and cartilage, 2009-05, Vol.17 (5), p.655-661

2009

Volltextzugriff (PDF)

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

Human genetics, 2013-10, Vol.132 (10), p.1077-1130

2013

Volltextzugriff (PDF)

Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility

Nature genetics, 2008-11, Vol.40 (11), p.1319-1323

2008

Volltextzugriff (PDF)

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

Human mutation, 2007-02, Vol.28 (2), p.150-158

2007

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)

Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics

Human mutation, 2010-06, Vol.31 (6), p.631-655

2010

Volltextzugriff (PDF)

comprehensive evaluation of SNP genotype imputation

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

2009

Volltextzugriff (PDF)

Human Gene Mutation Database (HGMD®): 2003 update

Human mutation, 2003-06, Vol.21 (6), p.577-581

2003

Volltextzugriff (PDF)

Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity

Human mutation, 2005-09, Vol.26 (3), p.205-213

2005

Volltextzugriff (PDF)

IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants

Nucleic acids research, 2017-02, Vol.45 (3), p.e13

2017

Volltextzugriff (PDF)

Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense

PloS one, 2015-07, Vol.10 (7), p.e0132150-e0132150

2015

Volltextzugriff (PDF)

VarWatch-A stand-alone software tool for variant matching

PloS one, 2019-04, Vol.14 (4), p.e0215618-e0215618

2019

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)

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

Human mutation, 2003-09, Vol.22 (3), p.229-244

2003

Volltextzugriff (PDF)

Neighboring-Nucleotide Effects on the Rates of Germ-Line Single-Base-Pair Substitution in Human Genes

American journal of human genetics, 1998-08, Vol.63 (2), p.474-488

1998

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)

The human gene mutation database

Trends in genetics, 1997-03, Vol.13 (3), p.121-122

1997

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)

Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity

Human mutation, 2003-01, Vol.21 (1), p.28-44

2003

Volltextzugriff (PDF)

1 – 25 von 93

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(90)
Mit Volltextzugriff
(88)

Publikationsform

Artikel
(90)
Buchkapitel
(3)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(77)
Humans
(74)
Life Sciences & Biomedicine
(71)
Genetics & Heredity
(51)
Biological And Medical Sciences
(28)
Mutation
(25)
Male
(20)
Medical Sciences
(20)
Genetic Diseases, Inborn - Genetics
(18)
Base Sequence
(17)
Female
(16)
Animals
(15)
Fundamental And Applied Biological Sciences. Psychology
(15)
Models, Genetic
(13)
Phenotype
(12)
Biochemistry & Molecular Biology
(11)
Genetic Variation
(11)
Genetics
(11)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(11)
Molecular Sequence Data
(11)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A Method to Cleave Target Molecules in a Neocartilage

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

Influence of bone morphogenetic protein-2 on the extracellular matrix, material properties, and gene expression of long-term articular chondrocyte cultures: loss of chondrocyte stability

Collagen 11a1 is indirectly activated by lymphocyte enhancer-binding factor 1 (Lef1) and negatively regulates osteoblast maturation

Effect of dermatan sulfate on the indentation and tensile properties of articular cartilage

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

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

Correlation between Genetic and Geographic Structure in Europe

Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics

comprehensive evaluation of SNP genotype imputation

Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 ( IL17REL )

Human Gene Mutation Database (HGMD®): 2003 update

Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity

IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants

Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense

VarWatch-A stand-alone software tool for variant matching

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

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

Neighboring-Nucleotide Effects on the Rates of Germ-Line Single-Base-Pair Substitution in Human Genes

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

The human gene mutation database

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

Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity

Suchergebnisse filtern