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A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy.A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucomaIncreased expression of MERTK is associated with a unique form of canine retinopathyGenetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders.An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.Skin microbiota and allergic symptoms associate with exposure to environmental microbes.Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs.Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease.Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.A putative silencer variant in a spontaneous canine model of retinitis pigmentosa
P50
Q33877378-722934B8-F06E-4E64-9002-1BE05256F7CEQ34457006-0D708D2E-9B9F-4B24-8302-43071EE90153Q35527147-DCA5BEFA-CCDE-4DDE-BF00-97A6A8768006Q36104089-FA3C4845-F5D5-4BEF-817E-5606ACA728FEQ38641705-07ED856D-0509-49A7-9E41-0DA56A5E2068Q52312091-5708D11C-A8CB-4F1B-91E4-0CC4E6D871F1Q55313237-283B56D7-AC49-47C2-8068-CFC2E9D2DAC7Q59695970-C4F7EFD3-13A6-436D-A9B2-D40FE897D6CDQ64910437-2CD4EB60-2A6A-4FAA-BF90-4509B7E59CB7Q90159827-A4C669A8-F4F9-4026-8D5D-05CB49B3B887
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
ricercatore
@it
wetenschapper
@nl
研究者
@zh
name
Maria Kaukonen
@ast
Maria Kaukonen
@en
Maria Kaukonen
@es
Maria Kaukonen
@nl
type
label
Maria Kaukonen
@ast
Maria Kaukonen
@en
Maria Kaukonen
@es
Maria Kaukonen
@nl
prefLabel
Maria Kaukonen
@ast
Maria Kaukonen
@en
Maria Kaukonen
@es
Maria Kaukonen
@nl
P31
P496
0000-0002-2146-4694