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...

Genetic parameters, genome-wide association study, and selection perspective on gestation length in 16 French cattle breeds

Journal of dairy science, 2024-10, Vol.107 (10), p.8157-8169

2024

Volltextzugriff (PDF)

Whole-genome analysis of introgressive hybridization and characterization of the bovine legacy of Mongolian yaks

Nature genetics, 2017-03, Vol.49 (3), p.470-475

2017

Volltextzugriff (PDF)

Uncovering Adaptation from Sequence Data: Lessons from Genome Resequencing of Four Cattle Breeds

Genetics (Austin), 2016-05, Vol.203 (1), p.433-450

2016

Volltextzugriff (PDF)

Nuclear sequences of mitochondrial origin in domestic yak

Scientific reports, 2024-05, Vol.14 (1), p.10217-10217, Article 10217

2024

Volltextzugriff (PDF)

Genome-wide association study with imputed whole-genome sequence variants including large deletions for female fertility in 3 Nordic dairy cattle breeds

Journal of dairy science, 2022-02, Vol.105 (2), p.1298-1313

2022

Volltextzugriff (PDF)

X-linked genes influence various complex traits in dairy cattle

BMC genomics, 2023-06, Vol.24 (1), p.338-338, Article 338

2023

Volltextzugriff (PDF)

A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle

Genetics selection evolution (Paris), 2024-05, Vol.56 (1), p.39-39, Article 39

2024

Volltextzugriff (PDF)

Rare cases of hernia of the linea alba among TWIST1 haploinsufficient Charolais cattle

Animal genetics, 2022-04, Vol.53 (2), p.239-241

2022

Volltextzugriff (PDF)

Targeted mutation and inactivation of the kinesin light chain 3 protein-encoding gene have no impact on mouse fertility

Biology of reproduction, 2024-01, Vol.110 (1), p.78-89

2024

Volltextzugriff (PDF)

Α de novo 3.8-Mb inversion affecting the EDA and XIST genes in a heterozygous female calf with generalized hypohidrotic ectodermal dysplasia

BMC genomics, 2019-09, Vol.20 (1), p.715-715, Article 715

2019

Volltextzugriff (PDF)

Are scurs in heterozygous polled (Pp) cattle a complex quantitative trait?

Genetics selection evolution (Paris), 2020-02, Vol.52 (1), p.6-6, Article 6

2020

Volltextzugriff (PDF)

Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets

Genome research, 2023-06, Vol.33 (6), p.957-971

2023

Volltextzugriff (PDF)

Integrin alpha 6 homozygous splice-site mutation causes a new form of junctional epidermolysis bullosa in Charolais cattle

Genetics selection evolution (Paris), 2023-06, Vol.55 (1), p.40-40, Article 40

2023

Volltextzugriff (PDF)

Massive detection of cryptic recessive genetic defects in dairy cattle mining millions of life histories

Genome Biology, 2024-09, Vol.25 (1), p.248-30, Article 248

2024

Volltextzugriff (PDF)

The 80-kb DNA duplication on BTA1 is the only remaining candidate mutation for the polled phenotype of Friesian origin

Genetics selection evolution (Paris), 2014-07, Vol.46 (1), p.44-44, Article 44

2014

Volltextzugriff (PDF)

A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse

Genetics selection evolution (Paris), 2017-11, Vol.49 (1), p.85-85, Article 85

2017

Volltextzugriff (PDF)

A newly described bovine type 2 scurs syndrome segregates with a frame-shift mutation in TWIST1

PloS one, 2011-07, Vol.6 (7), p.e22242-e22242

2011

Volltextzugriff (PDF)

Genomic regions underlying positive selection in local, Alpine cattle breeds

Animal genetics, 2023-06, Vol.54 (3), p.239-253

2023

Volltextzugriff (PDF)

An initiator codon mutation in SDE2 causes recessive embryonic lethality in Holstein cattle

Journal of dairy science, 2018-07, Vol.101 (7), p.6220-6231

2018

Volltextzugriff (PDF)

Identification of two new recessive MC1R alleles in red‐coloured Evolèner cattle and other breeds

Animal genetics, 2022-06, Vol.53 (3), p.427-435

2022

Volltextzugriff (PDF)

A de novo frameshift mutation in ZEB2 causes polledness, abnormal skull shape, small body stature and subfertility in Fleckvieh cattle

Scientific reports, 2020-10, Vol.10 (1), p.17032-17032, Article 17032

2020

Volltextzugriff (PDF)

A missense mutation in PFAS (phosphoribosylformylglycinamidine synthase) is likely causal for embryonic lethality associated with the MH1 haplotype in Montbéliarde dairy cattle

Journal of dairy science, 2017-10, Vol.100 (10), p.8176-8187

2017

Volltextzugriff (PDF)

Avant-propos : Anomalies génétiques

INRA Productions Animales, 2020-01, Vol.29 (5), p.293-296

2020

Volltextzugriff (PDF)

A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds

Genetics selection evolution (Paris), 2016-08, Vol.48 (1), p.56-56, Article 56

2016

Volltextzugriff (PDF)

Construction of a large collection of small genome variations in French dairy and beef breeds using whole-genome sequences

Genetics selection evolution (Paris), 2016-11, Vol.48 (1), p.87-87, Article 87

2016

Volltextzugriff (PDF)

1 – 25 von 49

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(48)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(49)

Sprache

Englisch
(49)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

Life Sciences
(47)
Science & Technology
(44)
Life Sciences & Biomedicine
(37)
Animals
(34)
Agriculture
(27)
Cattle
(27)
Genetics & Heredity
(23)
Male
(23)
Agriculture, Dairy & Animal Science
(22)
Female
(21)
Genomes
(21)
Mutation
(21)
Cattle - Genetics
(18)
Genomics
(18)
Genes
(15)
Genetics
(15)
Haplotypes
(15)
Genotype
(14)
Phenotype
(14)
Genetic Aspects
(13)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Genetic parameters, genome-wide association study, and selection perspective on gestation length in 16 French cattle breeds

Whole-genome analysis of introgressive hybridization and characterization of the bovine legacy of Mongolian yaks

Uncovering Adaptation from Sequence Data: Lessons from Genome Resequencing of Four Cattle Breeds

Nuclear sequences of mitochondrial origin in domestic yak

Genome-wide association study with imputed whole-genome sequence variants including large deletions for female fertility in 3 Nordic dairy cattle breeds

X-linked genes influence various complex traits in dairy cattle

A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle

Rare cases of hernia of the linea alba among TWIST1 haploinsufficient Charolais cattle

Targeted mutation and inactivation of the kinesin light chain 3 protein-encoding gene have no impact on mouse fertility

Α de novo 3.8-Mb inversion affecting the EDA and XIST genes in a heterozygous female calf with generalized hypohidrotic ectodermal dysplasia

Are scurs in heterozygous polled (Pp) cattle a complex quantitative trait?

Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets

Integrin alpha 6 homozygous splice-site mutation causes a new form of junctional epidermolysis bullosa in Charolais cattle

Massive detection of cryptic recessive genetic defects in dairy cattle mining millions of life histories

The 80-kb DNA duplication on BTA1 is the only remaining candidate mutation for the polled phenotype of Friesian origin

A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse

A newly described bovine type 2 scurs syndrome segregates with a frame-shift mutation in TWIST1

Genomic regions underlying positive selection in local, Alpine cattle breeds

An initiator codon mutation in SDE2 causes recessive embryonic lethality in Holstein cattle

Identification of two new recessive MC1R alleles in red‐coloured Evolèner cattle and other breeds

A de novo frameshift mutation in ZEB2 causes polledness, abnormal skull shape, small body stature and subfertility in Fleckvieh cattle

A missense mutation in PFAS (phosphoribosylformylglycinamidine synthase) is likely causal for embryonic lethality associated with the MH1 haplotype in Montbéliarde dairy cattle

Avant-propos : Anomalies génétiques

A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds

Construction of a large collection of small genome variations in French dairy and beef breeds using whole-genome sequences

Suchergebnisse filtern