Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control
about
Obsessive-compulsive disorder and related disorders: a comprehensive surveyMicroarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDA necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologuesGenetics of Prader-Willi syndrome and Prader-Will-Like syndromeGenome-wide and parental allele-specific analysis of CTCF and cohesin DNA binding in mouse brain reveals a tissue-specific binding pattern and an association with imprinted differentially methylated regionsGenomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionFrom microscopes to microarrays: dissecting recurrent chromosomal rearrangements.Insights into synaptic function from mouse models of human cognitive disorders.Imprinted genes and mental dysfunction.The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus.The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease.Prader-Willi Syndrome: Clinical and Genetic FindingsHeterochromatin dysregulation in human diseases.The imprinted gene and parent-of-origin effect database.Cloning of dexamethasone-induced transcript: a novel glucocorticoid-induced gene that is upregulated in emphysema.Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
P2860
Q21203920-14A2365B-703C-4021-9330-3E8A19B5DA08Q24676625-23824794-C4C5-465A-A499-C8CE24C75B80Q24797302-5B11E49D-4FD1-4724-BDDA-1F5334AF3A4DQ28074219-2CE7196F-2E61-4A9A-9A37-045BEB1EDBEAQ28586104-AC3DAF69-9937-4926-AAC2-D424918A93CAQ33316874-BB323641-0551-4380-9B64-58CCDE365986Q33805828-4C3DC427-FA51-439D-BE06-F3C65D0A5B09Q33964940-4C57CC4E-2E1F-4539-817A-A8515A11ECDEQ34093571-5CE6EDF5-29E7-4B15-AE65-DCA381F0A314Q34190554-09976D7A-D192-4219-A86B-FE51C06D7728Q34228077-E12AE9AB-BCF7-48BC-8E3B-0FDF5D7B1014Q34561533-44629918-FF46-4597-B4AF-E949F80EDCA8Q37201174-B9DF1A03-3A9C-41B3-8981-C0AC4D4B2007Q37723199-4566AE69-9CEB-4115-9485-B094170A19C0Q38661383-47FD2F4C-4683-44D2-ABD7-1332ECA1DBC3Q42655512-3DD77720-1B28-4010-96DA-D4D6C2B7A775Q48563558-65FC55DF-3894-4F5E-A134-A7534E485DB8
P2860
Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control
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2000 nî lūn-bûn
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2000 թուականի Մարտին հրատարակուած գիտական յօդուած
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2000 թվականի մարտին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Identification of novel imprin ...... or regional imprinting control
@ast
Identification of novel imprin ...... or regional imprinting control
@en
Identification of novel imprin ...... or regional imprinting control
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type
label
Identification of novel imprin ...... or regional imprinting control
@ast
Identification of novel imprin ...... or regional imprinting control
@en
Identification of novel imprin ...... or regional imprinting control
@nl
prefLabel
Identification of novel imprin ...... or regional imprinting control
@ast
Identification of novel imprin ...... or regional imprinting control
@en
Identification of novel imprin ...... or regional imprinting control
@nl
P2860
P3181
P356
P1476
Identification of novel imprin ...... or regional imprinting control
@en
P2860
P304
P3181
P356
10.1086/302817
P407
P577
2000-03-01T00:00:00Z