DNA oxidation as triggered by H3K9me2 demethylation drives estrogen-induced gene expression. - Wikidata - awgldk - TriplyDB

DNA oxidation as triggered by H3K9me2 demethylation drives estrogen-induced gene expression.

DNA oxidation as triggered by H3K9me2 demethylation drives estrogen-induced gene expression.

http://www.wikidata.org/entity/Q40026501

about

Developmental roles of the histone lysine demethylases PELP1 is a reader of histone H3 methylation that facilitates oestrogen receptor-alpha target gene activation by regulating lysine demethylase 1 specificity TRIM24 links a non-canonical histone signature to breast cancer H3K27 demethylation by JMJD3 at a poised enhancer of anti-apoptotic gene BCL2 determines ERα ligand dependency Targeted DNA methylation by homology-directed repair in mammalian cells. Transcription reshapes methylation on the repaired gene.DNA topology and transcription Epigenetics in breast cancer: what's new?Beyond oxidative stress: an immunologist's guide to reactive oxygen species Ocular herpes simplex virus: how are latency, reactivation, recurrent disease and therapy interrelated?The Structure of DNA-Bound Human Topoisomerase II Alpha: Conformational Mechanisms for Coordinating Inter-Subunit Interactions with DNA Cleavage Mitochondrial ROS and the Effectors of the Intrinsic Apoptotic Pathway in Aging Cells: The Discerning Killers!Histone methylation modifiers in cellular signaling pathways Local chromatin microenvironment determines DNMT activity: from DNA methyltransferase to DNA demethylase or DNA dehydroxymethylase KDM1 class flavin-dependent protein lysine demethylases Targeting the PELP1-KDM1 axis as a potential therapeutic strategy for breast cancer LSD1 inhibition: a therapeutic strategy in cancer?Base excision repair facilitates a functional relationship between Guanine oxidation and histone demethylation Oxygen consumption and usage during physical exercise: the balance between oxidative stress and ROS-dependent adaptive signaling LSD1-mediated demethylation of histone H3 lysine 4 triggers Myc-induced transcription The lysine specific demethylase-1 (LSD1/KDM1A) regulates VEGF-A expression in prostate cancer Topoisomerase IIbeta activates a subset of neuronal genes that are repressed in AT-rich genomic environment.Genome-wide mechanisms of nuclear receptor action.PRDM Proteins: Molecular Mechanisms in Signal Transduction and Transcriptional Regulation.Vitamin D and the epigenome.Metabolic control of the epigenome in systemic Lupus erythematosus.Class I lysine deacetylases promote glucocorticoid-induced transcriptional repression through functional interaction with LSD1.Control of alpha-herpesvirus IE gene expression by HCF-1 coupled chromatin modification activities.Location analysis for the estrogen receptor-alpha reveals binding to diverse ERE sequences and widespread binding within repetitive DNA elements.Direct visualization of repair of oxidative damage by OGG1 in the nuclei of live cells.The endogenous exposome.Base excision repair: a critical player in many games 3D shortcuts to gene regulation A time-invariant principle of genome evolution.DNA break mapping reveals topoisomerase II activity genome-wide.Epigenetic switch at atp2a2 and myh7 gene promoters in pressure overload-induced heart failure.Genome-wide progesterone receptor binding: cell type-specific and shared mechanisms in T47D breast cancer cells and primary leiomyoma cells.8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress Nuclear receptor-induced transcription is driven by spatially and timely restricted waves of ROS. The role of Akt, IKKα, and DNA damage repair enzymes.The molecular pathology of schizophrenia--focus on histone and DNA modifications Mechanism of retinoic acid-induced transcription: histone code, DNA oxidation and formation of chromatin loops.

P2860

Q22306162-70FBE0C4-ECD9-4F7F-A08F-A437520B1AA4 Q24310502-87C7D48D-0C5B-478F-8669-C49933F5CBBB Q24317243-C03BBDC4-8AEF-43BD-86B3-A7D466FEDB66 Q24322697-9F316860-FEBC-4163-98D7-8DAB6C0D7223 Q24613629-6D64D849-B50F-41EE-A8EB-843D7CB1ED7D Q26865092-ED034CAE-6956-4969-9A55-6A9854F78536 Q26991779-C44B0E03-9E98-40D5-B7D7-C2442028120A Q27011356-1714C12C-A9CB-4DCA-BB10-5BB15FD3673E Q27021069-44434B84-AF8B-4513-A7A7-7B85F9755840 Q27670934-2D3FCE27-21A9-4872-86E7-3056B20EE5D2 Q28068299-7374CC54-AC28-4712-B1B3-7A0D80345E94 Q28082123-4C305197-F3FC-484F-848B-4AC58FFAC746 Q28084375-688C2841-9E12-43AE-8FED-11B952B25FE7 Q28084876-04D1BEF8-5C0E-488F-9967-375B60941053 Q28271388-CF3DD839-7FA2-4288-9671-C7464EB12CB5 Q28274561-9D9E7AF6-1678-4301-A4B8-A26C29D4215C Q28283078-0D6634A0-40E6-41E5-8535-3C1AD6266E24 Q28394742-4A53BE5C-ED25-4A2C-936A-0CFA32E69A19 Q28564742-CB7B7E60-6840-4D80-B175-B2D5C6C235D4 Q28687241-4A47320A-625A-49E3-AC6A-78DF58FDA42A Q33396673-4A3608BC-881A-4085-9DA6-A6C3265B75F7 Q33508325-6D3971C4-ED4B-4AE5-AEAB-07F2D634F627 Q33565484-636CF0A9-4A13-4474-9CC9-BECA12F6EF4D Q33569349-55BEFABC-1B7A-4861-A19F-23F919599E92 Q33664849-A3367859-8985-4BEC-9591-AF4C7B814150 Q33727032-59494EDD-FB43-47B0-8C45-8B8D669A08B2 Q33729222-F019150B-7544-4DB4-8195-B6B350F0B164 Q33783157-0D36B229-0DF4-4702-9C72-2583FF750614 Q33820755-C79AA549-0CC7-413D-BE8D-87497C03F999 Q33898288-819C282C-5AA1-4174-9A37-333C9A5067AF Q33908163-EEDDA6AD-1523-43FC-AE1D-91116E9E8F13 Q34047673-EB363837-BD2F-4C01-ACFF-8435D78E8AE6 Q34059478-B68EBE46-463E-47ED-B29E-B20E05539F36 Q34072605-FB977C4C-B8C6-49E0-9E5D-B8A7ECD01748 Q34121851-76561A2F-7676-4F4B-A3DC-A8820C070B0C Q34137268-012B366E-FAD8-4AB9-AA63-2F4E68D2C460 Q34147844-52CED3C8-F7AF-4E31-8C8E-266FE05A13B9 Q34183355-401BA30C-EC50-41A5-8688-71415BB53927 Q34236086-6B75FD1D-79E3-4B44-A909-E8F08D13E615 Q34248924-A54B7661-5113-46E7-8AEA-FEDB3B9150A3

P2860

DNA oxidation as triggered by H3K9me2 demethylation drives estrogen-induced gene expression.

http://www.wikidata.org/entity/Q40026501

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

DNA oxidation as triggered by ...... rogen-induced gene expression.

@en

type

label

DNA oxidation as triggered by ...... rogen-induced gene expression.

@en

prefLabel

DNA oxidation as triggered by ...... rogen-induced gene expression.

@en

P1433

Q40026501-B763836D-4336-4D8B-B14A-4EECDF4CEE1F

P1476

Q40026501-2E87A356-A262-4F23-81AF-E1A16BE6C066

P2093

Q40026501-1063CE20-9D15-423E-90FF-48D019D7DFF9

Q40026501-64431503-BF71-400B-9006-581C7EA68520

Q40026501-90F55418-F11D-430C-AE13-4B1BD301F29A

Q40026501-94619376-A26F-4486-88C8-D3E0EB9645E6

Q40026501-9FDF92EE-2B61-4578-8DD9-83EFD3E10210

Q40026501-AB3CE04B-627D-408C-B8E6-599D09B4C23D

Q40026501-BABF5678-177C-4539-BAE5-E75D90E3EE3F

Q40026501-C497E54F-657D-4714-B478-F4C3174287A9

Q40026501-DA0176B6-8EB9-404C-AD63-0EAAD7BBD564

Q40026501-F8D66111-60A4-4DD8-883A-00FF8AA35BED

P2860

Q40026501-0AEE691A-92F9-4E83-B678-98A7140A1357

Q40026501-1049360B-7AB4-4645-800F-740495A6F1C8

Q40026501-2CEC5784-15E3-4046-801A-45044F93D06A

Q40026501-2EECDB3D-654A-44C6-938E-84D6A1573F6A

Q40026501-2F51972B-9453-4A2D-8C03-3903299A3DB3

Q40026501-32E8D4D9-B5FE-4D79-A916-E89B6D29BA6D

Q40026501-33788A34-0BA1-4F59-BA73-8B46CE1D20EC

Q40026501-357D4237-378C-446E-AE93-B726AD786393

Q40026501-4BF5DFB3-040E-4528-8025-E494962E93D8

Q40026501-65FA162E-CF5B-4B0A-A158-D773E188AAEC

P304

Q40026501-4A1AD16B-5F72-4EE7-ABE6-D0B7C4EEE49F

P31

Q40026501-00971520-62E0-45DA-9BEC-7677A8A94D88

P356

Q40026501-39FD8D89-82F6-4F78-AEE0-04C84D832CE5

P407

Q40026501-F380734E-E36B-4F51-81AA-C9B36D39A4C5

P433

Q40026501-EF2A9FA8-AB0C-4C23-AAC6-A239A0DA10D9

P478

Q40026501-4D5D556F-A299-4B5C-A324-8290D7273476

P577

Q40026501-00B9911C-57A7-4C2C-8CB9-CAF0CAC40C84

P5875

Q40026501-556EB555-FF96-4BA0-9F3E-2CF8A61569BB

P698

Q40026501-A771D21F-91F8-4955-91BB-1798855530CB

P356

SCIENCE.1147674

P1433

P1476

DNA oxidation as triggered by ...... rogen-induced gene expression.

@en

P2093

Alessandra Bertoni

http://www.w3.org/2001/XMLSchema#string

Annarita Sasso

http://www.w3.org/2001/XMLSchema#string

Antonio Malorni

http://www.w3.org/2001/XMLSchema#string

Bruno Perillo

http://www.w3.org/2001/XMLSchema#string

Ciro Abbondanza

http://www.w3.org/2001/XMLSchema#string

Concetta Cuozzo

http://www.w3.org/2001/XMLSchema#string

Enrico V Avvedimento

http://www.w3.org/2001/XMLSchema#string

Lorenzo Chiariotti

http://www.w3.org/2001/XMLSchema#string

Maria Neve Ombra

http://www.w3.org/2001/XMLSchema#string

Silvana Sacchetti

http://www.w3.org/2001/XMLSchema#string

P2860

Translating the Histone Code

The catalytic subunit of the proteasome is engaged in the entire process of estrogen receptor-regulated transcription

Histone demethylation mediated by the nuclear amine oxidase homolog LSD1

Functional and physical interaction between the histone methyl transferase Suv39H1 and histone deacetylases

The nuclear receptor superfamily: the second decade

The language of covalent histone modifications

Molecular cloning and functional expression of a human cDNA encoding the antimutator enzyme 8-hydroxyguanine-DNA glycosylase

Cofactor dynamics and sufficiency in estrogen receptor-regulated transcription

Base-excision repair of oxidative DNA damage

Estrogen receptor-alpha directs ordered, cyclical, and combinatorial recruitment of cofactors on a natural target promoter

P304

202-206

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1126/SCIENCE.1147674

http://www.w3.org/2001/XMLSchema#string

P407

P433

5860

http://www.w3.org/2001/XMLSchema#string

P478

319

http://www.w3.org/2001/XMLSchema#string

P577

2008-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5662448

http://www.w3.org/2001/XMLSchema#string

P698

18187655

http://www.w3.org/2001/XMLSchema#string