A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.

A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.

A novel X-linked gene, DXS8237E, was isolated from human fetal brain cDNA, and its 3' end was mapped to within 20 kb upstream of UBE1 in Xp11.23. A 1.3-kb cDNA for DXS8237E detects homologous sequences in other mammals and a 3-kb mRNA that is widely expressed in human cell lines and mouse tissu...

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Bibliografische gegevens
Hoofdauteurs:	Coleman, M, Ambrose, H, Carrel, L, Németh, A, Willard, H, Davies, K
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	1996

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AN INTEGRATED PHYSICAL, GENETIC AND TRANSCRIPTIONAL MAP IN XP11.23
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Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
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A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.
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TRANSCRIPTION FACTOR GENES ZNF21, ZNF81, AND ELK1 MAP TO A 400-KB REGION BETWEEN THE OATL1 AND PFC LOCI AT XP11.23
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A 1.8-Mb YAC contig in Xp11.23: identification of CpG islands and physical mapping of CA repeats in a region of high gene density.
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Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locus.
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PRIMERS FOR THE DINUCLEOTIDE REPEAT AT THE DXS453 LOCUS ALSO RECOGNIZES THE DXS983 LOCUS
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DXS106 AND DXS559 FLANK THE X-LINKED DYSTONIA-PARKINSONISM LOCUS, DYT3
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Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.
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DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).
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Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.
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Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
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2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
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LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES
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Genetic analysis of DXS101and DXS6807 short tandem repeat (X-STR) in samples of Iraqi Arab male population
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Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.
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The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YAC.
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Recurrent fever of unknown origin and unexplained bacteremia in a patient with a novel 4.5 Mb microdeletion in Xp11.23-p11.22
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A 2.6-MB YAC CONTIG OF THE HUMAN X-INACTIVATION CENTER REGION IN XQ13 - PHYSICAL LINKAGE OF THE RPS4X, PHKA1, XIST, AND DXS128E GENES AND REFINEMENT OF THE XIC-CONTAINING INTERVAL
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The evolution of radio sources in the UKIDSS-DXS-XMM-LSS field
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Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX.
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Identification of Inhibitors of the Anti-Infective Target DXS Using Dynamic Combinatorial Chemistry
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A Novel Aurora-A Inhibitor (MLN8237) Synergistically Enhances the Antitumor Activity of Sorafenib in Hepatocellular Carcinoma
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Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.
door: Hatton, C, et al.
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Layer by layer encapsulation of PRM/DXS/neutravidin and antibody on calcium carbonate core
door: Liaw, Zi Yen.
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Induction of Terpene Biosynthesis in Berries of Microvine Transformed with VvDXS1 Alleles
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An exploratory phase 2 study of investigational Aurora A kinase inhibitor alisertib (MLN8237) in acute myelogenous leukemia and myelodysplastic syndromes
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Mayo Clinic experience with 1123 adults with acute myeloid leukemia
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Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
door: Fischbeck, K, et al.
Gepubliceerd in: (1986)

Cloning and expression characterisation of LiDXS2 gene in Oriental Lily (Lilium 'Sorbonne')
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