Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region
about
Core histones and HIRIP3, a novel histone-binding protein, directly interact with WD repeat protein HIRAIdentification of human gene products containing Pro-Pro-x-Tyr (PY) motifs that enhance glutathione and endocytotic marker uptake in yeastDeficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduriaPhysiological and pathological roles of mitochondrial SLC25 carriersOrganization and sequence of the human gene for the mitochondrial citrate transport proteinTranscriptional Regulation of the Mitochondrial Citrate and Carnitine/Acylcarnitine Transporters: Two Genes Involved in Fatty Acid Biosynthesis and β-oxidation.Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.Probing the effect of transport inhibitors on the conformation of the mitochondrial citrate transport protein via a site-directed spin labeling approach.Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.Transcriptional regulation of cardiac development: implications for congenital heart disease and DiGeorge syndrome.Differential effects of coconut oil- and fish oil-enriched diets on tricarboxylate carrier in rat liver mitochondria.n-6 PUFAs downregulate expression of the tricarboxylate carrier in rat liver by transcriptional and posttranscriptional mechanisms.The KRAB zinc finger gene ZNF74 encodes an RNA-binding protein tightly associated with the nuclear matrix.Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.First pass annotation of promoters on human chromosome 22.Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.How many breaks do we need to CATCH on 22q11?Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.phosphoenolpyruvate
P2860
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P2860
Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Localization of the human mito ...... eorge syndrome critical region
@ast
Localization of the human mito ...... eorge syndrome critical region
@en
Localization of the human mito ...... eorge syndrome critical region
@en-gb
Localization of the human mito ...... eorge syndrome critical region
@nl
type
label
Localization of the human mito ...... eorge syndrome critical region
@ast
Localization of the human mito ...... eorge syndrome critical region
@en
Localization of the human mito ...... eorge syndrome critical region
@en-gb
Localization of the human mito ...... eorge syndrome critical region
@nl
prefLabel
Localization of the human mito ...... eorge syndrome critical region
@ast
Localization of the human mito ...... eorge syndrome critical region
@en
Localization of the human mito ...... eorge syndrome critical region
@en-gb
Localization of the human mito ...... eorge syndrome critical region
@nl
P2093
P356
P1433
P1476
Localization of the human mito ...... eorge syndrome critical region
@en
P2093
A Langeveld
J ten Hoeve
M P Mulder
N Heisterkamp
P356
10.1006/GENO.1995.9982
P407
P577
1995-09-20T00:00:00Z