about
P688
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathwaysKnockout of the mouse apolipoprotein B gene results in embryonic lethality in homozygotes and protection against diet-induced hypercholesterolemia in heterozygotesapo B gene knockout in mice results in embryonic lethality in homozygotes and neural tube defects, male infertility, and reduced HDL cholesterol ester and apo A-I transport rates in heterozygotesA targeted apolipoprotein B-38.9-producing mutation causes fatty livers in mice due to the reduced ability of apolipoprotein B-38.9 to transport triglyceridesA deficiency of microsomal triglyceride transfer protein reduces apolipoprotein B secretionA novel functional role for apolipoprotein B in male infertility in heterozygous apolipoprotein B knockout miceReduced intestinal fat absorptive capacity but enhanced susceptibility to diet-induced fatty liver in mice heterozygous for ApoB38.9 truncationTwo distinct apolipoprotein B alleles in mice generated by a single 'in-out' targetingDelayed arteriogenesis in hypercholesterolemic miceA gene-targeted mouse model for familial hypobetalipoproteinemia. Low levels of apolipoprotein B mRNA in association with a nonsense mutation in exon 26 of the apolipoprotein B geneSusceptibility to atherosclerosis in mice expressing exclusively apolipoprotein B48 or apolipoprotein B100Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in miceHeterozygous mutation of ataxia-telangiectasia mutated gene aggravates hypercholesterolemia in apoE-deficient miceA targeted apoB38.9 mutation in mice is associated with reduced hepatic cholesterol synthesis and enhanced lipid peroxidationRegulation of the apolipoprotein B in heterozygous hypobetalipoproteinemic knock-out mice expressing truncated apoB, B81. Low production and enhanced clearance of apoB cause low levels of apoBDual mechanisms for the low plasma levels of truncated apolipoprotein B proteins in familial hypobetalipoproteinemia. Analysis of a new mouse model with a nonsense mutation in the Apob geneMicrosomal triacylglycerol transfer protein is required for lumenal accretion of triacylglycerol not associated with ApoB, as well as for ApoB lipidationDefining the atherogenicity of large and small lipoproteins containing apolipoprotein B100Hepatic secretion of apoB-100 is impaired in hypobetalipoproteinemic mice with an apoB-38.9-specifying alleleThe effects of apolipoprotein F deficiency on high density lipoprotein cholesterol metabolism in mice
P921
Q24296634-12A6DA52-B022-49B8-8B0F-AAB371973D52Q24563247-AB201854-02CC-4D6E-95DD-915EFF4F876AQ28507091-9D7C99EB-B2A6-4D90-BB1F-923F6913CC86Q28507306-3A97A47D-0674-4576-A2D9-2DD0BDC4FDCCQ28507431-B5CF41D6-BE60-4DB8-B71A-DA58560493CEQ28508453-59C25815-1533-490E-AC9D-E23975663760Q28508454-0686FCAD-83DC-4327-8273-9B0F80F1FCD2Q28510806-62460DD0-202B-4EA2-A165-AF2E9B24191DQ28511993-48758354-E02D-4DBE-BDAB-330AD0C3CE1CQ28512923-14D33772-898F-4C56-8C2A-FF25C2F2FEA5Q28513997-9DCA29D7-6AD5-4E78-8868-B9CC3BA2B5E6Q28584854-95FD8EF5-6A9D-4677-B960-D0D4C15F090FQ28585377-573B10FA-D90B-46AA-B376-E8E45C89C283Q28585589-BF668BAF-3EA0-48F5-8AE5-914C46B144C8Q28585994-67C6B93A-503D-4BB5-9780-5BF652843E2DQ28589650-B411CD1B-4FCF-4E93-A08D-39B14B798351Q28590076-419E43A4-CB80-40DE-8B37-BB52B7EFE96AQ28590506-412D5B22-6AC8-41D6-AC85-A386D91EC864Q28593031-7EDDC446-8E3E-476C-B5F7-1ABA27E82FD8Q28594692-DB48DDA7-D6CA-45A1-9084-DE0E98B2B6AA
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Apolipoprotein B
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
Apolipoprotein B
@en
Apolipoprotein B
@nl
type
label
Apolipoprotein B
@en
Apolipoprotein B
@nl
altLabel
Apob
@en
apolipoprotein B-100
@en
uniprot:E9Q414
@en
prefLabel
Apolipoprotein B
@en
Apolipoprotein B
@nl
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XP_006515141
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ENSMUSP00000035761
ENSMUSP00000036044
ENSMUSP00000127147
ENSMUSP00000129496