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...

Phase-Aware Web Browser Power Management on HMP Platforms

Proceedings of the 2018 International Conference on Supercomputing, 2018, p.274-283

2018

Volltextzugriff (PDF)

API for power-aware application design on mobile systems

2018 IEEE/ACM 5th International Conference on Mobile Software Engineering and Systems (MOBILESoft), 2018, p.90-91

2018

Volltextzugriff (PDF)

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

PLoS genetics, 2011-10, Vol.7 (10), p.e1002316-e1002316

2011

Volltextzugriff (PDF)

Antihypertensive action of drug combination: polythiazide, prazosin and tolamolol

Current therapeutic research, 1977-02, Vol.21 (2), p.169

1977

Volltextzugriff (PDF)

Dog colour patterns explained by modular promoters of ancient canid origin

Nature ecology & evolution, 2021-10, Vol.5 (10), p.1415-1423

2021

Volltextzugriff (PDF)

Antihypertensive drug combinations: prazosin, hydrochlorothiazide and clonidine

Annals of clinical research, 1977-10, Vol.9 (5), p.296

1977

Volltextzugriff (PDF)

A putative silencer variant in a spontaneous canine model of retinitis pigmentosa

PLoS genetics, 2020-03, Vol.16 (3), p.e1008659-e1008659

2020

Volltextzugriff (PDF)

A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease

PLoS genetics, 2015-04, Vol.11 (4), p.e1005169-e1005169

2015

Volltextzugriff (PDF)

Intronic variant in POU1F1 associated with canine pituitary dwarfism

Human genetics, 2021-11, Vol.140 (11), p.1553-1562

2021

Volltextzugriff (PDF)

Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders

PloS one, 2016-08, Vol.11 (8), p.e0161005-e0161005

2016

Volltextzugriff (PDF)

Intronic variant in POU1F1 associated with canine pituitary dwarfism

Yearbook of Paediatric Endocrinology, 2022-09

2022

Volltextzugriff (PDF)

An across-breed validation study of 46 genetic markers in canine hip dysplasia

BMC genomics, 2021-01, Vol.22 (1), p.68-68, Article 68

2021

Volltextzugriff (PDF)

Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10

PloS one, 2013-09, Vol.8 (9), p.e75621-e75621

2013

Volltextzugriff (PDF)

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

PLoS genetics, 2019-09, Vol.15 (9), p.e1008378-e1008378

2019

Volltextzugriff (PDF)

TSEN54 missense variant in Standard Schnauzers with leukodystrophy

PLoS genetics, 2019-10, Vol.15 (10), p.e1008411-e1008411

2019

Volltextzugriff (PDF)

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats

PLoS genetics, 2022-06, Vol.18 (6), p.e1009804-e1009804

2022

Volltextzugriff (PDF)

Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs

PLoS genetics, 2020-03, Vol.16 (3), p.e1008651-e1008651

2020

Volltextzugriff (PDF)

Altered Basal Autophagy Affects Extracellular Vesicle Release in Cells of Lagotto Romagnolo Dogs With a Variant ATG4D

Veterinary pathology, 2020-11, Vol.57 (6), p.926-935

2020

Volltextzugriff (PDF)

Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

PLoS genetics, 2020-01, Vol.16 (1), p.e1008527-e1008527

2020

Volltextzugriff (PDF)

Joint Formal Comment for PLGE and Commentary for G3

G3 : genes - genomes - genetics, 2020-11, Vol.10 (11), p.3881-3881

2020

Volltextzugriff (PDF)

A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia

Scientific reports, 2019-01, Vol.9 (1), p.973-973, Article 973

2019

Volltextzugriff (PDF)

A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery

PLoS genetics, 2012-06, Vol.8 (6), p.e1002759-e1002759

2012

Volltextzugriff (PDF)

Evaluating intrusion prevention systems with evasions

International journal of communication systems, 2017-11, Vol.30 (16), p.n/a

2017

Volltextzugriff (PDF)

Disease Progression and Treatment Response of Idiopathic Epilepsy in Australian Shepherd Dogs

Journal of veterinary internal medicine, 2012-01, Vol.26 (1), p.116-125

2012

Volltextzugriff (PDF)

Genome‐wide association study in mice identifies loci affecting liver‐related phenotypes including Sel1l influencing serum bile acids

Hepatology (Baltimore, Md.), 2016-06, Vol.63 (6), p.1943-1956

2016

Volltextzugriff (PDF)

1 – 25 von 40

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(31)

Publikationsform

Sprache

Englisch
(39)
Finnisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Phase-Aware Web Browser Power Management on HMP Platforms

API for power-aware application design on mobile systems

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

Antihypertensive action of drug combination: polythiazide, prazosin and tolamolol

Dog colour patterns explained by modular promoters of ancient canid origin

Antihypertensive drug combinations: prazosin, hydrochlorothiazide and clonidine

A putative silencer variant in a spontaneous canine model of retinitis pigmentosa

A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease

Intronic variant in POU1F1 associated with canine pituitary dwarfism

Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders

Intronic variant in POU1F1 associated with canine pituitary dwarfism

An across-breed validation study of 46 genetic markers in canine hip dysplasia

Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

TSEN54 missense variant in Standard Schnauzers with leukodystrophy

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats

Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs

Altered Basal Autophagy Affects Extracellular Vesicle Release in Cells of Lagotto Romagnolo Dogs With a Variant ATG4D

Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

Joint Formal Comment for PLGE and Commentary for G3

A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia

A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery

Evaluating intrusion prevention systems with evasions

Disease Progression and Treatment Response of Idiopathic Epilepsy in Australian Shepherd Dogs

Genome‐wide association study in mice identifies loci affecting liver‐related phenotypes including Sel1l influencing serum bile acids

Suchergebnisse filtern