Lista de obras - Doreen Becker - Dominio Público Uruguay

A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle

artículo científico publicado en 2020

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

artículo científico publicado en 2017

A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy

artículo científico publicado en 2010

A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars

artículo científico publicado en 2013

A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep

artículo científico publicado en 2020

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

artículo científico publicado en 2015

A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta

artículo científico publicado en 2009

A variant in MYO10 is associated with hind limb conformation in Swiss Large White boars

artículo científico publicado en 2013

An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs

artículo científico publicado en 2014

Canine NAPEPLD-associated models of human myelin disorders.

artículo científico publicado en 2018

Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses

artículo científico publicado en 2020

Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration

scientific article published on 07 February 2019

Cows selected for divergent mastitis susceptibility display a differential liver transcriptome profile after experimental Staphylococcus aureus mammary gland inoculation

artículo científico publicado en 2020

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness

artículo científico publicado en 2019

Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene

artículo científico publicado en 2010

Molecular studies of phenotype variation in canine RPGR-XLPRA1.

artículo científico publicado en 2016

Optic nerve hypoplasia in miniature poodle dogs: A preliminary genetic and candidate gene association study

scientific article published on 25 July 2019

Single-cell RNA sequencing of freshly isolated bovine milk cells and cultured primary mammary epithelial cells

publication published on 15 July 2021

The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8.

artículo científico publicado en 2014

Wattles in goats are associated with the FMN1/GREM1 region on chromosome 10.

artículo científico publicado en 2015

[A case of SRY positive sex reversal in a domestic cat]

artículo científico publicado en 2015

[Cytogenetical and molecular analyses in a horse with SRY-negative sex reversal]

scientific article published on 01 July 2014

Lista de obras de Doreen Becker

A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy

A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars

A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep

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

A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta

A variant in MYO10 is associated with hind limb conformation in Swiss Large White boars

An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs

Canine NAPEPLD-associated models of human myelin disorders.

Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses

Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration

Cows selected for divergent mastitis susceptibility display a differential liver transcriptome profile after experimental Staphylococcus aureus mammary gland inoculation

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness

Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene

Molecular studies of phenotype variation in canine RPGR-XLPRA1.

Optic nerve hypoplasia in miniature poodle dogs: A preliminary genetic and candidate gene association study

Single-cell RNA sequencing of freshly isolated bovine milk cells and cultured primary mammary epithelial cells

The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8.

Wattles in goats are associated with the FMN1/GREM1 region on chromosome 10.

[A case of SRY positive sex reversal in a domestic cat]

[Cytogenetical and molecular analyses in a horse with SRY-negative sex reversal]