Chromatin Remodeling in Development and Disease: Focus on CHD7
article has not abstract
Vyšlo v časopise:
Chromatin Remodeling in Development and Disease: Focus on CHD7. PLoS Genet 6(7): e32767. doi:10.1371/journal.pgen.1001010
Kategorie:
Perspective
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1001010
Souhrn
article has not abstract
Zdroje
1. VissersLE
van RavenswaaijCM
AdmiraalR
HurstJA
de VriesBB
2004 Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet 36 955 957
2. ZentnerGE
LaymanWS
MartinDM
ScacheriPC
2010 Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. Am J Med Genet A 152A 674 686
3. BosmanEA
PennAC
AmbroseJC
KettleboroughR
StempleDL
2005 Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Hum Mol Genet 14 3463 3476
4. HurdEA
CapersPL
BlauwkampMN
AdamsME
RaphaelY
2007 Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues. Mamm Genome 18 94 104
5. SchnetzMP
BartelsCF
ShastriK
BalasubramanianD
ZentnerGE
2009 Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns. Genome Res 19 590 601
6. SchnetzMP
HandokoL
Akhtar-ZaidiB
BartelsCF
PereiraCF
2010 CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression. PLoS Genet 6(7) e1001023 doi:10.1371/journal.pgen.1001023
7. BajpaiR
ChenDA
Rada-IglesiasA
ZhangJ
XiongY
2010 CHD7 cooperates with PBAF to control multipotent neural crest formation. Nature 463 958 962
8. HoL
JothiR
RonanJL
CuiK
ZhaoK
2009 An embryonic stem cell chromatin remodeling complex, esBAF, is an essential component of the core pluripotency transcriptional network. Proc Natl Acad Sci U S A 106 5187 5191
9. TakadaI
MiharaM
SuzawaM
OhtakeF
KobayashiS
2007 A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation. Nat Cell Biol 9 1273 1285
10. LaymanWS
McEwenDP
BeyerLA
LalaniSR
FernbachSD
2009 Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Hum Mol Genet 18 1909 1923
11. HoL
CrabtreeGR
2010 Chromatin remodelling during development. Nature 463 474 484
12. De SarioA
2009 Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation. Eur J Med Genet 52 363 372
13. BagchiA
PapazogluC
WuY
CapursoD
BrodtM
2007 CHD5 is a tumor suppressor at human 1p36. Cell 128 459 475
14. PeoplesRJ
CiscoMJ
KaplanP
FranckeU
1998 Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23. Cytogenet Cell Genet 82 238 246
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2010 Číslo 7
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- Extensive DNA End Processing by Exo1 and Sgs1 Inhibits Break-Induced Replication
- Question and Answer: An Anniversary Interview with Jane Gitschier
- Multi-Variant Pathway Association Analysis Reveals the Importance of Genetic Determinants of Estrogen Metabolism in Breast and Endometrial Cancer Susceptibility
- Lysosomal Dysfunction Promotes Cleavage and Neurotoxicity of Tau