about
Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.Identification and preliminary characterization of mouse Adam33Genetic analysis of attractin homologsFunctional annotation and ENUMGRN1-dependent pigment-type switching requires its ubiquitination activity but not its interaction with TSG101 or NEDD4Transgenic analysis of the physiological functions of Mahogunin Ring Finger-1 isoformsLevels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion diseaseDisrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice.Genetic and biochemical studies of the Agouti-attractin system.Mitochondrial dysfunction precedes neurodegeneration in mahogunin (Mgrn1) mutant miceAbnormal regulation of TSG101 in mice with spongiform neurodegeneration.RML prions act through Mahogunin and Attractin-independent pathways.Shades of meaning: the pigment-type switching system as a tool for discovery.Lack of prolidase causes a bone phenotype both in human and in mouse.Juvenile-onset loss of lipid-raft domains in attractin-deficient mice.Genetic and phenotypic studies of the dark-like mutant mouse.Genetic analysis of ventricular arrhythmia in young German Shepherd Dogs.Fast, exact linkage analysis for categorical traits on arbitrary pedigree designs.Development of the cerebellar defect in ataxic SELH/Bc mice.Characterization of Mahogunin Ring Finger-1 expression in mice.Exencephaly and cleft cerebellum in SELH/Bc mouse embryos are alternative developmental consequences of the same underlying genetic defect.Meeting report of the 26th International Mammalian Genome Conference.Developmental cardiac hypertrophy in a mouse model of prolidase deficiency.Distribution of Mahogany/Attractin mRNA in the rat central nervous system.Mice with mutations in Mahogunin ring finger-1 (Mgrn1) exhibit abnormal patterning of the left-right axis.Cardiomyocyte calcium cycling in a naturally occurring German shepherd dog model of inherited ventricular arrhythmia and sudden cardiac deathEvaluation of a fibrillin 2 gene haplotype associated with hip dysplasia and incipient osteoarthritis in dogsPiecing together the pigment-type switching puzzleIdentification and characterization of canine microsatellite markers in cardiac genesCanine microsatellites associated with genes implicated in cardiac development and functionGenetically determined absence of an initiation site of cranial neural tube closure is causally related to exencephaly in SELH/Bc mouse embryosChronic and age-dependent effects of the spongiform neurodegeneration-associated MGRN1 E3 ubiquitin ligase on mitochondrial homeostasis
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
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name
Teresa M. Gunn
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Teresa M. Gunn
@en
Teresa M. Gunn
@es
Teresa M. Gunn
@nl
Teresa M. Gunn
@sl
type
label
Teresa M. Gunn
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Teresa M. Gunn
@en
Teresa M. Gunn
@es
Teresa M. Gunn
@nl
Teresa M. Gunn
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prefLabel
Teresa M. Gunn
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Teresa M. Gunn
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Teresa M. Gunn
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Teresa M. Gunn
@nl
Teresa M. Gunn
@sl
P106
P1153
7005013292
P21
P31
P496
0000-0003-2688-6420