about
P688
Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairmentDramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseasesMice deficient in all forms of lysosomal beta-hexosaminidase show mucopolysaccharidosis-like pathologyDeletion of macrophage-inflammatory protein 1 alpha retards neurodegeneration in Sandhoff disease miceNeuronal accumulation of alpha- and beta-synucleins in the brain of a GM2 gangliosidosis mouse modelLysosomal dysfunction and impaired autophagy in a novel mouse model deficient for the lysosomal membrane protein Cln7A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorderalpha-Galactosidase A deficient mice: a model of Fabry diseaseMice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity.Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosidesDynamics of major histocompatibility complex class II compartments during B cell receptor-mediated cell activationExpression of c-fos and c-myc in satellite cell cultures from dystrophic mdx and control mouse muscleDevelopment of infertility at young adult age in a mouse model of human Sandhoff diseaseInhibition of calcium uptake via the sarco/endoplasmic reticulum Ca2+-ATPase in a mouse model of Sandhoff disease and prevention by treatment with N-butyldeoxynojirimycinSpecific induction of macrophage inflammatory protein 1-alpha in glial cells of Sandhoff disease model mice associated with accumulation of N-acetylhexosaminyl glycoconjugatesPhospholipid synthesis is decreased in neuronal tissue in a mouse model of Sandhoff diseaseSperm require beta-N-acetylglucosaminidase to penetrate through the egg zona pellucidaMouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolismNo requirement for V(D)J recombination in p53-deficient thymic lymphomaMice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosisSpecificity of mouse GM2 activator protein and beta-N-acetylhexosaminidases A and B. Similarities and differences with their human counterparts in the catabolism of GM2Reduced pigmentation (rp), a new coat colour gene with effects on kidney lysosomal glycosidases in the mouse
P921
Q28504760-EB481665-34DE-4C38-8BDA-6B4125B7974AQ28506454-36326106-9035-44AE-973F-DA5657FC7DCDQ28507414-662EBEFC-24BF-42DE-9966-70848FC33972Q28507753-82041F60-3938-44F3-A1A7-F49520196A7DQ28509735-F2871722-FAE5-42A7-9176-58A39BEBC86BQ28510746-077FF3B2-CCCB-4B04-B7DD-A85FC5DDC66BQ28511052-AD2D41E0-834F-4972-A98F-E91CBB1DF3B5Q28513530-FD6882DB-53B2-4321-952F-C8DBEFF6CA47Q28584902-339C6DB5-181A-4355-9F3B-AE7A0814BEC4Q28585326-E0FF2B15-D1D6-484E-86E7-8787F7B8D5CBQ28585845-AE0431FE-DC99-487A-AEAE-12764F6EA99CQ28586904-25D7821E-4856-4ED9-9C5F-B73B53F8F734Q28587313-41714F57-FD1E-4F8F-A5AC-9947CCF7E8DAQ28587559-55AE83DA-1B85-4298-B945-779EF311A116Q28589857-E0AAF3BF-6507-46E6-BFEE-7D6B54F3147BQ28590773-19902679-2ACC-4218-B887-3142D233B589Q28592818-23C53DD0-F0A7-41E5-94BC-95C552DF15BCQ28593406-F1D0762B-3380-4156-B22E-9E87EF695E4CQ28594411-3C92BED6-48CC-4299-B0FC-778A5BFB769CQ28594483-32F36A0B-F435-4686-95F4-0CA410F29B9FQ28594978-56080249-3CAB-40B0-A675-FCE39D1A7A8CQ70682506-46417C03-0DF4-4E86-AC4B-C36C7DBA85F0
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Hexosaminidase B
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
Hexosaminidase B
@en
Hexosaminidase B
@nl
type
label
Hexosaminidase B
@en
Hexosaminidase B
@nl
altLabel
Hexb
@en
N-acetyl-beta-glucosaminidase subunit beta
@en
beta-N-acetylhexosaminidase subunit beta
@en
beta-hexosaminidase subunit beta
@en
hexosaminidase subunit B
@en
prefLabel
Hexosaminidase B
@en
Hexosaminidase B
@nl
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ENSMUSP00000022169