A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
about
sameAs
Characterization of conserved and nonconserved imprinted genes in swineThe odyssey of MeCP2 and parental imprintingDLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiencyComputational and experimental identification of novel human imprinted genesA family of neofunctionalized Ty3/gypsy retrotransposon genes in mammalian genomesParaoxonase 1 activities and polymorphisms in autism spectrum disordersLoss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndromeGenetic and molecular analyses of PEG10 reveal new aspects of genomic organization, transcription and translationNovel gene expression patterns along the proximo-distal axis of the mouse embryo before gastrulation.Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes.Persistent DNA methylation changes associated with prenatal mercury exposure and cognitive performance during childhoodDifferentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.Genome-wide prediction of imprinted murine genesPossible genomic imprinting of three human obesity-related genetic loci.Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism.Selective expression of sense and antisense transcripts of the sushi-ichi-related retrotransposon--derived family during mouse placentogenesisThe role of imprinted genes in fetal growth abnormalities.Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.Imprinted genes in placental growth and obstetric disorders.Importance of the matriline for genomic imprinting, brain development and behaviour.DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex.Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.Investigation of parent-of-origin effect in comitant strabismus using MOD score analysisAn SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.Assessment of imprinting- and genetic variation-dependent monoallelic expression using reciprocal allele descendants between human family trios.Genome-wide assessment of imprinted expression in human cells.Identification of direct downstream targets of Dlx5 during early inner ear development.Absent expression of the osteoblast-specific maternally imprinted genes, DLX5 and DLX6, causes split hand/split foot malformation type I.Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay.Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.Direct evidence of allele equivalency at the Dlx5/6 locus.Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
P2860
Q24647126-C5565D73-8EC1-4D6C-AA42-7053FC0BECBAQ24671994-22F5F5C3-261F-4CB1-86AB-478491E72042Q24677959-E48337C9-7A7B-41D8-AC58-7D1ED5611862Q24684684-AD0E0E6C-30DF-4B02-939D-8BDDCF3B9F66Q28266640-906E08F1-429C-4A92-8266-6F9472D919C1Q28390802-5E7E960C-D7A8-4456-B968-CB85AB5D84DBQ28592236-CA9E431A-4E75-428A-9338-5AE9406BEA3EQ28749419-FC5B8EE1-28F2-454C-BCA1-D32A67BE1DC6Q30359895-268FD06C-6577-42AF-AD3E-38850F2CC629Q33557441-E04482FC-2BDD-4A04-88DF-79E74D637748Q33671228-05B3DA24-5706-49D8-BA3A-5C48FC9E1609Q33740660-49676AE3-35F8-46C8-86E1-247E3DA1FFC3Q33841575-1662711C-8F21-4558-B565-C6D65D3CE56EQ33938638-6E299F5F-5ED3-4C5E-98AD-47CE1C0A3F11Q34327305-45CF7388-C790-4D52-98BF-4A8D70DB8190Q35121889-4A62D49C-FB4D-4995-BF3D-4CDBE7DDB403Q35295496-70962669-19D8-4669-9BE8-6AB3FBCA4EBAQ35447807-6A0461B6-990D-460C-A1FA-5AA5F320F9D8Q36436588-F51933F3-028D-497B-AE28-6031C651F966Q36515797-DA53B085-37B5-42AB-BF3D-F81BDD7826D4Q36684143-62C5A4F3-AE82-4433-B730-6855F8CEDC41Q36804837-FB882D4F-93AC-4A41-96BA-B107E443CFCAQ37258692-DC8D3C9E-935E-4FE2-AD9F-21704312F4E5Q38430761-5FDB54B6-CD41-4D6E-B0E2-BFA079E4C62DQ38647931-804A861F-BAC8-478B-9039-EC59976D6D62Q39573980-BE5774A3-CA88-4FB8-A35E-E4300C48AF32Q39608750-AD94405C-9BAA-46BE-AD6A-E7C55C2EDE8BQ40230295-8F552506-3E4E-4CAA-A537-224E10A31C6EQ42078835-55423916-3B89-48DD-8324-425A28CF56B2Q42676707-AE503575-5529-427B-97A5-CB935C088842Q42681078-980CAD58-21C1-4AD9-A40A-2A8BED050736Q46534463-4129CA8B-C26A-4D1C-BAD4-3D021DA02ABC
P2860
A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@ast
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@en
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@nl
type
label
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@ast
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@en
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@nl
prefLabel
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@ast
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@en
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@nl
P2093
P1433
P1476
A new imprinted cluster on the ...... -mouse monochromosomal hybrids
@en
P2093
Chiga Okita
Hidetoshi Hoshiya
Makiko Meguro
Masayuki Haruta
Mitsuo Oshimura
Yu-ki Sakamoto
P356
10.1016/S0888-7543(03)00052-1
P407
P577
2003-06-01T00:00:00Z