UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 2.832

Sortiert nach

High-throughput marker assays for FaRPc2-mediated resistance to Phytophthora crown rot in octoploid strawberry

Molecular breeding, 2018-08, Vol.38 (8), p.1-11, Article 104

2018

Link zum Volltext

Verfügbarkeit prüfen

BoLA-DIB: species distribution, linkage with DOB, and Northern analysis

Animal genetics, 1993-02, Vol.24 (1), p.41-45

1993

Link zum Volltext

Verfügbarkeit prüfen

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP

American journal of human genetics, 2012-03, Vol.90 (3), p.502-510

2012

Link zum Volltext

Verfügbarkeit prüfen

Partial nucleotide sequence of a novel bovine major histocompatibility complex class II β‐chain gene, BoLA‐DIB

Animal genetics, 1990-01, Vol.21 (4), p.353-360

1990

Link zum Volltext

Verfügbarkeit prüfen

A conserved role for p48 homologs in protecting dopaminergic neurons from oxidative stress

PLoS genetics, 2014-10, Vol.10 (10), p.e1004718-e1004718

2014

Link zum Volltext

Verfügbarkeit prüfen

Cerebrospinal Fluid C1-Esterase Inhibitor and Tie-1 Levels Affect Cognitive Performance: Evidence from Proteome-Wide Mendelian Randomization

Genes, 2024-01, Vol.15 (1), p.71

2024

Link zum Volltext

Verfügbarkeit prüfen

De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy

Journal of medical genetics, 2015-05, Vol.52 (5), p.330-337

2015

Link zum Volltext

Verfügbarkeit prüfen

Virus-mediated shRNA knockdown of Na(v)1.3 in rat dorsal root ganglion attenuates nerve injury-induced neuropathic pain

Molecular therapy, 2013-01, Vol.21 (1), p.49-56

2013

Link zum Volltext

Verfügbarkeit prüfen

Spondyloocular Syndrome: A Report of an Additional Family and Phenotypic Spectrum Delineation

Genes, 2023-02, Vol.14 (2), p.497

2023

Link zum Volltext

Verfügbarkeit prüfen

Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus

BMC medical genetics, 2011-09, Vol.12 (1), p.129-129, Article 129

2011

Link zum Volltext

Verfügbarkeit prüfen

A generalized mechanistic codon model

Molecular biology and evolution, 2014-09, Vol.31 (9), p.2528-2541

2014

Link zum Volltext

Verfügbarkeit prüfen

Multi-locus sequencing typing reveals geographically related intraspecies variability of Sporothrix brasiliensis

Fungal genetics and biology, 2024-02, Vol.170, p.103845-103845, Article 103845

2024

Link zum Volltext

Verfügbarkeit prüfen

HLA Genotypes and Type 1 Diabetes and Its Relationship to Reported Race/Skin Color in Their Relatives: A Brazilian Multicenter Study

Genes, 2022-05, Vol.13 (6), p.972

2022

Link zum Volltext

Verfügbarkeit prüfen

Impact of achondroplasia on Latin American patients: a systematic review and meta-analysis of observational studies

Orphanet journal of rare diseases, 2022-01, Vol.17 (1), p.4-4, Article 4

2022

Link zum Volltext

Verfügbarkeit prüfen

Nomenclature for factors of the BoLA system, 1996: report of the ISAG BoLA Nomenclature Committee

Animal genetics, 1997-06, Vol.28 (3), p.159-168

1997

Link zum Volltext

Verfügbarkeit prüfen

Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

Frontiers in genetics, 2022-08, Vol.13, p.900574-900574

2022

Link zum Volltext

Verfügbarkeit prüfen

Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome

American journal of human genetics, 2010-08, Vol.87 (2), p.265-273

2010

Link zum Volltext

Verfügbarkeit prüfen

Pri smORF Peptides Are Wide Mediators of Ecdysone Signaling, Contributing to Shape Spatiotemporal Responses

Frontiers in genetics, 2021-08, Vol.12, p.714152-714152

2021

Link zum Volltext

Verfügbarkeit prüfen

Angiogenic gene therapy in patients with nonrevascularizable ischemic heart disease: a phase 2 randomized, controlled trial of AdVEGF (AdVEGF121) versus maximum medical treatment

Gene therapy, 2006-11, Vol.13 (21), p.1503-1511

2006

Link zum Volltext

Verfügbarkeit prüfen

Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes

Advances in genetics, 2008, Vol.63, p.85

2008

Link zum Volltext

Verfügbarkeit prüfen

TYMS promotes genomic instability and tumor progression in Ink4a/Arf null background

Oncogene, 2023-06, Vol.42 (23), p.1926-1939

2023

Link zum Volltext

Verfügbarkeit prüfen

Association between HLA Class II Alleles/Haplotypes and Genomic Ancestry in Brazilian Patients with Type 1 Diabetes: A Nationwide Exploratory Study

Genes, 2023-04, Vol.14 (5), p.991

2023

Link zum Volltext

Verfügbarkeit prüfen

Identification and evaluation of reference genes for expression studies by RT-qPCR during embryonic development of the emerging model organism, Macrobrachium olfersii

Gene, 2017-01, Vol.598, p.97-106

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 2.832

Suche als RSS-Feed

Aktive Filter

ThemaGenetics & Heredity

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.703)
Mit Volltextzugriff
(2.637)

Publikationsform

Artikel
(2.828)
Buchkapitel
(4)

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(2.830)
Science & Technology
(2.830)
Humans
(2.303)
Biological And Medical Sciences
(1.407)
Female
(1.321)
Male
(1.272)
Medical Sciences
(1.053)
Chromosome Mapping
(944)
Pedigree
(799)
Genetics
(754)
Animals
(547)
Genetic Markers
(545)
Genetic Linkage
(531)
Biochemistry & Molecular Biology
(500)
Biotechnology & Applied Microbiology
(471)
Fundamental And Applied Biological Sciences. Psychology
(464)
Adult
(463)
Mutation
(458)
Molecular Sequence Data
(455)

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

American Journal Of Human Genetics
(361)
Genomics
(228)
American Journal Of Medical Genetics
(200)
Journal Of Medical Genetics
(140)
Human Molecular Genetics
(119)
Genes Chromosomes & Cancer
(112)
European Journal Of Human Genetics : Ejhg
(110)
The American Journal Of Human Genetics
(104)
Human Genetics
(94)
Nature Genetics
(78)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

High-throughput marker assays for FaRPc2-mediated resistance to Phytophthora crown rot in octoploid strawberry

BoLA-DIB: species distribution, linkage with DOB, and Northern analysis

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP

Partial nucleotide sequence of a novel bovine major histocompatibility complex class II β‐chain gene, BoLA‐DIB

A conserved role for p48 homologs in protecting dopaminergic neurons from oxidative stress

Cerebrospinal Fluid C1-Esterase Inhibitor and Tie-1 Levels Affect Cognitive Performance: Evidence from Proteome-Wide Mendelian Randomization

De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy

Virus-mediated shRNA knockdown of Na(v)1.3 in rat dorsal root ganglion attenuates nerve injury-induced neuropathic pain

Spondyloocular Syndrome: A Report of an Additional Family and Phenotypic Spectrum Delineation

Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus

A generalized mechanistic codon model

Multi-locus sequencing typing reveals geographically related intraspecies variability of Sporothrix brasiliensis

HLA Genotypes and Type 1 Diabetes and Its Relationship to Reported Race/Skin Color in Their Relatives: A Brazilian Multicenter Study

Impact of achondroplasia on Latin American patients: a systematic review and meta-analysis of observational studies

Nomenclature for factors of the BoLA system, 1996: report of the ISAG BoLA Nomenclature Committee

Whole-methylome analysis of circulating monocytes in acute diabetic Charcot foot reveals differentially methylated genes involved in the formation of osteoclasts

Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome

Pri smORF Peptides Are Wide Mediators of Ecdysone Signaling, Contributing to Shape Spatiotemporal Responses

Angiogenic gene therapy in patients with nonrevascularizable ischemic heart disease: a phase 2 randomized, controlled trial of AdVEGF (AdVEGF121) versus maximum medical treatment

Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes

TYMS promotes genomic instability and tumor progression in Ink4a/Arf null background

Association between HLA Class II Alleles/Haplotypes and Genomic Ancestry in Brazilian Patients with Type 1 Diabetes: A Nationwide Exploratory Study

Identification and evaluation of reference genes for expression studies by RT-qPCR during embryonic development of the emerging model organism, Macrobrachium olfersii

De novo TRPV4 Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathy

Aktive Filter

Suchergebnisse filtern