Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain
about
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolutionNew insights into establishment and maintenance of DNA methylation imprints in mammalsEpigenetic virtues of chromodomainsA non-coding RNA within the Rasgrf1 locus in mouse is imprinted and regulated by its homologous chromosome in transStructural Insight into Recognition of Methylated Histone Tails by Retinoblastoma-binding Protein 1Retinoblastoma-binding Protein 1 Has an Interdigitated Double Tudor Domain with DNA Binding ActivityGenetics of Prader-Willi syndrome and Prader-Will-Like syndromeARID4A and ARID4B regulate male fertility, a functional link to the AR and RB pathwaysIdentification of chromatin remodeling genes Arid4a and Arid4b as leukemia suppressor genesAndrogen Receptor Coactivator ARID4B Is Required for the Function of Sertoli Cells in SpermatogenesisRetinoblastoma binding protein-1 (RBP1) is a Runx2 coactivator and promotes osteoblastic differentiation.Retinoblastoma and its binding partner MSI1 control imprinting in Arabidopsis.Retinoblastoma makes its mark on imprinting in plants.The function of non-coding RNAs in genomic imprinting.Mouse models of myelodysplastic syndromes.Successful computational prediction of novel imprinted genes from epigenomic features.Mammalian genomic imprinting.Generation of novel pharmacogenomic candidates in response to methotrexate in juvenile idiopathic arthritis: correlation between gene expression and genotype.Allelic variation and differential expression of the mSIN3A histone deacetylase complex gene Arid4b promote mammary tumor growth and metastasis.Complex network-driven view of genomic mechanisms underlying Parkinson's disease: analyses in dorsal motor vagal nucleus, locus coeruleus, and substantia nigraGenome-wide patterns of genetic variation in two domestic chickens.Histone H3 trimethylation at lysine 36 is associated with constitutive and facultative heterochromatin.Epigenetic memory in mammals.Identification of imprinting regulators at the Meg3 differentially methylated regionG9a histone methyltransferase contributes to imprinting in the mouse placenta.PR-SET7 and SUV4-20H regulate H4 lysine-20 methylation at imprinting control regions in the mouse.Keeping things quiet: roles of NuRD and Sin3 co-repressor complexes during mammalian development.Genomic imprinting: employing and avoiding epigenetic processes.Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.Heterochromatin dysregulation in human diseases.Molecular mechanisms of genomic imprinting and clinical implications for cancer.Histone methylation in myelodysplastic syndromes.Metastasis suppression by BRMS1 associated with SIN3 chromatin remodeling complexes.Tudor domain-containing proteins of Drosophila melanogaster.Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications.Temporal-Spatial Establishment of Initial Niche for the Primary Spermatogonial Stem Cell Formation Is Determined by an ARID4B Regulatory Network.Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndromeDistinguishing epigenetic marks of developmental and imprinting regulation.Recommendations for the investigation of animal models of Prader-Willi syndrome.Imprinting analysis in the Acrodysplasia region of mouse chromosome 12.
P2860
Q21092496-5719B133-C1C3-47FF-923A-021D5F78FF34Q26852971-3579A9C5-B784-4E71-A6A4-C3EBF04B38BDQ27016161-E3773683-1041-4C6B-9BBE-2B47DEFC48DEQ27317100-38674C90-32BA-4BC7-A2EA-712E18B0961FQ27676760-B2CE098B-A771-4616-9CB7-6BCB76723544Q27681142-B04BBD53-66FF-4E01-89E5-11871E3DB1ADQ28074219-9152446A-AA21-4575-9389-57F9E29E78A5Q28588957-E67F39D7-8114-4867-B6E7-6D54730B7282Q28592846-099FE697-1A01-4A91-83A8-A7ABE870D3DDQ30356888-C9842D36-DB89-46A7-A2B5-7B2EF3D7AB2AQ30983671-86B91509-12B3-4FDC-98BE-4B120012DADEQ33359855-58C5BC62-0BCA-43E6-9F9E-A94AE687AD28Q33364222-A1FACEE3-8EDF-4554-A8FD-419C49533056Q33761870-C4E6FDC8-E57F-4849-B892-D4409D6C3DDDQ33767319-A36F9412-5E81-4701-A02D-8F8C6A54D8DDQ33963896-747921FA-0507-4540-9383-F4DA8A158A2FQ34026917-D0282D81-C4CF-44D1-94EC-F641277ABAA7Q34235121-BD67FA36-BF31-487A-8307-734860CE4116Q34302171-F28FEFC4-777E-4B14-AF81-25DEE6BF374BQ34667486-B40E8ECC-EC02-490D-B57E-273A79F071BBQ34787581-C3D0381F-F462-45CC-89DE-4386BDD40668Q35195947-B1A058F7-66E6-46A5-B270-DAEBEB998CE3Q35711156-D1C90971-8CA8-43EC-A1D6-1E9B009B9CD1Q36192047-7BD8D927-9930-4102-B914-D8A7E1975B67Q36421353-66956ABC-980E-4387-A76F-48B7C7358484Q36851813-DBB265D5-BA66-4BA2-9DFB-1168E6E8EFDEQ37262437-4F16F139-F41F-4A22-BEE5-1D15FD7755E0Q37362832-DD97CEE9-7426-466D-BC42-4275FB8665A1Q37397396-55B94CE4-262C-49F0-BAE6-10DCA20E1DECQ37723199-CF8B838D-B076-4088-83F5-FF92BF54B30DQ37831991-199249CB-55E5-4A36-949C-CFE55BCE4B7BQ37961859-4B0EE5A1-892C-4DA5-8556-1F487A5343E1Q38017096-783F798E-EC5B-4957-B648-3CE3360D3BBDQ38112434-214C114C-DCC2-43FD-9494-9425C7128743Q38166841-E69387B1-CBC8-4EEC-8BE3-F1BB5FF40433Q38716189-EA5EFACD-37BF-4E6C-8221-2EF6B45C5567Q38724302-02D896A7-3997-4735-B3A7-6F1FFF900A0FQ39697159-67F94FDA-89B2-43BF-ADE2-52B5BDF9FA14Q44803556-C9E4EF0D-8CB6-48ED-ABD5-D3657FAD54F5Q51934816-4DEDD780-BD59-4503-BB95-62330937F1E5
P2860
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain
description
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im Oktober 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/10/15)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/10/15)
@nl
наукова стаття, опублікована в жовтні 2006
@uk
مقالة علمية (نشرت في 15-10-2006)
@ar
name
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@ast
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@en
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@nl
type
label
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@ast
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@en
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@nl
prefLabel
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@ast
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@en
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@nl
P2093
P2860
P3181
P356
P1433
P1476
Deficiency of Rbbp1/Arid4a and ...... ng defect in the PWS/AS domain
@en
P2093
Arthur L. Beaudet
Ting-Fen Tsai
P2860
P304
P3181
P356
10.1101/GAD.1452206
P577
2006-10-15T00:00:00Z