The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.
about
Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)Conformational response to ligand binding in phosphomannomutase2: insights into inborn glycosylation disorder.Molecular analysis of phosphomannomutase (PMM) genes reveals a unique PMM duplication event in diverse Triticeae species and the main PMM isozymes in bread wheat tissues.A deeply divergent phosphoglucomutase (PGM) of Giardia lamblia has both PGM and phosphomannomutase activities.Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethalityHighlights of glycosylation and adhesion related genes involved in myogenesis.Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.Insufficient ER-stress response causes selective mouse cerebellar granule cell degeneration resembling that seen in congenital disorders of glycosylation.Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphataseBiochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylationA mutant of phosphomannomutase1 retains full enzymatic activity, but is not activated by IMP: Possible implications for the disease PMM2-CDG.Molecular cloning and functional analysis of the phosphomannomutase (PMM) gene from Dendrobium officinale and evidence for the involvement of an abiotic stress response during germination.CDG Therapies: From Bench to Bedside.The Trim family of genes and the retina: Expression and functional characterization
P2860
Q27311626-D26B6ADD-3072-4EAF-AB98-D6FE1A30A768Q30607614-F626B794-C511-493F-BA99-342433708678Q33710239-A0503C7B-2926-4632-86FD-A0ED6E0BC518Q34169536-02E4F180-8AB6-4D5E-9170-AD0F2698BBF1Q35070998-F5171641-2FF4-4542-8B06-95734BE55FADQ35211154-094BA22D-AD7C-447C-A7A1-6F0FE40CA3ACQ37429297-A8378F1C-0781-4DCF-A0DC-DE5C41AB1EFFQ37532964-E5D8F7A1-67CC-41DD-833A-EE111787122BQ39928511-4F7F7E2F-E51C-4346-B208-C199FAD12335Q41874177-C01851A1-8588-4788-B635-47242720FBA2Q47121667-01B49C82-2384-4AE2-A8A0-362C64117DFEQ50469011-8C732782-4111-4B20-A04E-28C18EB0987FQ52558429-1A0568D5-F190-4D03-A1B0-81244B7B1F5FQ58748039-AD310B48-1D66-4CC3-8098-407B2CB63C6D
P2860
The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
The normal phenotype of Pmm1-d ...... for normal mouse development.
@ast
The normal phenotype of Pmm1-d ...... for normal mouse development.
@en
type
label
The normal phenotype of Pmm1-d ...... for normal mouse development.
@ast
The normal phenotype of Pmm1-d ...... for normal mouse development.
@en
prefLabel
The normal phenotype of Pmm1-d ...... for normal mouse development.
@ast
The normal phenotype of Pmm1-d ...... for normal mouse development.
@en
P2093
P2860
P356
P1476
The normal phenotype of Pmm1-d ...... for normal mouse development.
@en
P2093
Cromphout K
De Deyn PP
Hartmann D
Heykants L
Keldermans L
Matthijs G
Schollen E
P2860
P304
P356
10.1128/MCB.02357-05
P407
P577
2006-08-01T00:00:00Z