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Marine Actinomycetes, New Sources of Biotechnological Products

Marine drugs, 2021-06, Vol.19 (7), p.365

2021

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A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves

Animal genetics, 2019-12, Vol.50 (6), p.695-704

2019

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Comprehensive characterization of horse genome variation by whole‐genome sequencing of 88 horses

Animal genetics, 2019-02, Vol.50 (1), p.74-77

2019

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A novel MLPH variant in dogs with coat colour dilution

Animal genetics, 2018-02, Vol.49 (1), p.94-97

2018

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A novel KIT deletion variant in a German Riding Pony with white‐spotting coat colour phenotype

Animal genetics, 2019-12, Vol.50 (6), p.761-763

2019

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A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle

Animal genetics, 2016-04, Vol.47 (2), p.253-257

2016

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Compound heterozygosity for TNXB genetic variants in a mixed‐breed dog with Ehlers‐Danlos syndrome

Animal genetics, 2019-10, Vol.50 (5), p.546-549

2019

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A deletion spanning the promoter and first exon of the hair cycle‐specific ASIP transcript isoform in black and tan rabbits

Animal genetics, 2020-02, Vol.51 (1), p.137-140

2020

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A missense variant in the NSDHL gene in a Chihuahua with a congenital cornification disorder resembling inflammatory linear verrucous epidermal nevi

Animal genetics, 2019-12, Vol.50 (6), p.768-771

2019

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A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism

Animal genetics, 2017-10, Vol.48 (5), p.619-621

2017

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In silico and in vitro analysis of genetic variants of the equine CYP3A94, CYP3A95 and CYP3A97 isoenzymes

Toxicology in vitro, 2019-10, Vol.60, p.116-124

2019

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Asian horses deepen the MSY phylogeny

Animal genetics, 2018-02, Vol.49 (1), p.90-93

2018

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A frameshift variant in the COL5A1 gene in a cat with Ehlers‐Danlos syndrome

Animal genetics, 2018-12, Vol.49 (6), p.641-644

2018

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Thorium utilization in existing and advanced reactor types

International journal of hydrogen energy, 2016-05, Vol.41 (17), p.7094-7102

2016

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Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes

Animal genetics, 2017-08, Vol.48 (4), p.483-485

2017

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Performance comparison of hysteresis pulse width modulation and space vector pulse width modulation techniques for torque ripple reduction in permanent magnet synchronous motor using iterative learning control

Journal of vibration and control, 2014-04, Vol.20 (5), p.698-712

2014

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A non‐coding regulatory variant in the 5′‐region of the MITF gene is associated with white‐spotted coat in Brown Swiss cattle

Animal genetics, 2019-02, Vol.50 (1), p.27-32

2019

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Whole‐genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness

Animal genetics, 2019-04, Vol.50 (2), p.172-174

2019

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A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex

Animal genetics, 2020-10, Vol.51 (5), p.829-832

2020

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Incorporation of interface current method based on 2D CP approach in VISWAM code system for hexagonal geometry

Annals of nuclear energy, 2016-06, Vol.92, p.161-174

2016

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Corrigendum: A second KRT71 allele in curly coated dogs

Animal genetics, 2021-08, Vol.52 (4), p.575-575

2021

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Two MC1R loss‐of‐function alleles in cream‐coloured Australian Cattle Dogs and white Huskies

Animal genetics, 2018-08, Vol.49 (4), p.284-290

2018

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Safety and efficacy of angiotensin-converting enzyme inhibitors in symptomatic severe aortic stenosis: symptomatic cardiac obstruction–pilot study of enalapril in aortic stenosis (SCOPE-AS)

The American heart journal, 2004-04, Vol.147 (4), p.740-740

2004

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Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog

Molecular genetics and metabolism, 2017-03, Vol.120 (3), p.269-277

2017

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Genetic variability of the equine casein genes

Journal of dairy science, 2016-07, Vol.99 (7), p.5486-5497

2016

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Marine Actinomycetes, New Sources of Biotechnological Products

A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves

Comprehensive characterization of horse genome variation by whole‐genome sequencing of 88 horses

A novel MLPH variant in dogs with coat colour dilution

A novel KIT deletion variant in a German Riding Pony with white‐spotting coat colour phenotype

A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle

Compound heterozygosity for TNXB genetic variants in a mixed‐breed dog with Ehlers‐Danlos syndrome

A deletion spanning the promoter and first exon of the hair cycle‐specific ASIP transcript isoform in black and tan rabbits

A missense variant in the NSDHL gene in a Chihuahua with a congenital cornification disorder resembling inflammatory linear verrucous epidermal nevi

A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism

In silico and in vitro analysis of genetic variants of the equine CYP3A94, CYP3A95 and CYP3A97 isoenzymes

Asian horses deepen the MSY phylogeny

A frameshift variant in the COL5A1 gene in a cat with Ehlers‐Danlos syndrome

Thorium utilization in existing and advanced reactor types

Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes

Performance comparison of hysteresis pulse width modulation and space vector pulse width modulation techniques for torque ripple reduction in permanent magnet synchronous motor using iterative learning control

A non‐coding regulatory variant in the 5′‐region of the MITF gene is associated with white‐spotted coat in Brown Swiss cattle

Whole‐genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness

A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex

Incorporation of interface current method based on 2D CP approach in VISWAM code system for hexagonal geometry

Corrigendum: A second KRT71 allele in curly coated dogs

Two MC1R loss‐of‐function alleles in cream‐coloured Australian Cattle Dogs and white Huskies

Safety and efficacy of angiotensin-converting enzyme inhibitors in symptomatic severe aortic stenosis: symptomatic cardiac obstruction–pilot study of enalapril in aortic stenosis (SCOPE-AS)

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog

Genetic variability of the equine casein genes

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