New insights reveal complex mechanisms involved in genomic imprinting.
about
The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivationDiscovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy.The mechanisms involved in formation of deletions and duplications of 15q11-q13.Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor.Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity.Genomic imprinting: a chromatin connectionPatterns of maternal transmission in bipolar affective disorder.Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method.The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunctionMaternal and paternal genomes function independently in mouse ova in establishing expression of the imprinted genes Snrpn and Igf2r: no evidence for allelic trans-sensing and counting mechanisms.Spatial and temporal silencing of the human maternal UBE3A gene.Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection.Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.Angelman syndrome in three biological siblings: Focusing on the neuropsychiatric domain.Dynamic methylation adjustment and counting as part of imprinting mechanisms.The dilemma of diagnostic testing for Prader-Willi syndromeGenetics of bipolar affective disorder: time for another reinvention?
P2860
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P2860
New insights reveal complex mechanisms involved in genomic imprinting.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
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1994年论文
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name
New insights reveal complex mechanisms involved in genomic imprinting.
@en
New insights reveal complex mechanisms involved in genomic imprinting.
@nl
type
label
New insights reveal complex mechanisms involved in genomic imprinting.
@en
New insights reveal complex mechanisms involved in genomic imprinting.
@nl
prefLabel
New insights reveal complex mechanisms involved in genomic imprinting.
@en
New insights reveal complex mechanisms involved in genomic imprinting.
@nl
P2860
P1476
New insights reveal complex mechanisms involved in genomic imprinting
@en
P2093
R D Nicholls
P2860
P304
P407
P577
1994-05-01T00:00:00Z