Literature DB >> 11673406

Human diseases with underlying defects in chromatin structure and modification.

B Hendrich1, W Bickmore.   

Abstract

Chromatin structure is important for regulating gene expression and for the proper condensation and segregation of chromosomes during cell division. Several human genetic diseases have been found to be due to mutations in genes producing proteins known or suspected to be involved in maintaining or modifying chromatin structure. Here we describe these 'chromatin diseases' and review what is known about the associated chromatin proteins in light of recent advances in the understanding of chromatin components, modification and function.

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Year:  2001        PMID： 11673406     DOI： 10.1093/hmg/10.20.2233

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


  28 in total

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3.  Evolutionary conservation of histone modifications in mammals.

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5.  BET bromodomain inhibition suppresses transcriptional responses to cytokine-Jak-STAT signaling in a gene-specific manner in human monocytes.

Authors:  Chun Hin Chan; Celestia Fang; Anna Yarilina; Rab K Prinjha; Yu Qiao; Lionel B Ivashkiv
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7.  In silico evidence for sequence-dependent nucleosome sliding.

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Review 9.  Combination therapy: histone deacetylase inhibitors and platinum-based chemotherapeutics for cancer.

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10.  Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes.

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