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DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 an…

Baquedano(María Sonia),Perez Garrido(Natalia… Mol Cell Endocrinol 0000-00-00

...RARB, NR4A1 and HSD3B2 genes in human adrenal tissues (HAT) and in pediatric virilizing adrenocortical tumors (VAT) were...

Evaluation of a subset of tumor suppressor gene for copy number and epigenitic …

Mariano(Fernanda Viviane),Egal(Erika Said),P… Oral Surg Oral Med Oral Patho… 0000-00-00

...RARB genes were associated with PA and CXPA, while KLK3 and AI69125 copy number losses were exclusive to CXPA. The sarco...

Novel epigenetic changes in CDKN2A are associated with progression of cervical …

Wijetunga(N Ari),Belbin(Thomas J),Burk(Rober… Gynecol Oncol 0000-00-00

...RARB, RASSF1, TERT and TIMP3 using the Illumina Infinium array. Validation was performed using high resolution mapping o...

Anteroposterior Patterning of Gene Expression in the Human Infant Sclera: Chond…

Seko(Yuko),Azuma(Noriyuki),Yokoi(Tadashi),Ka… Curr Eye Res 0000-00-00

...RARB were significantly higher in the posterior than in the anterior sclera of two independent infant eyes. Conversely, ...

miRNA-106a directly targeting RARB associates with the expression of Na(+)/I(-)…

Shen(Chen-Tian),Qiu(Zhong-Ling),Song(Hong-Ju… J Exp Clin Cancer Res 0000-00-00

...RARB) 3'-UTR. miR-106a-RARB promoted viability of thyroid cancer cells by regulating MEKK2-ERK1/2 and MEKK2-ERK5 pathway...

Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause…

Lopez(Estelle),Berenguer(Marie),Tingaud-Sequ… J Med Genet 0000-00-00

...RARB), whereas mutated MYT1 did not.,We report MYT1 as the first gene implicated in OAVS, within the RA signalling pathw...

Methylation pattern analysis in prostate cancer tissue: identification of bioma…

Gurioli(Giorgia),Salvi(Samanta),Martignano(F… J Transl Med 0000-00-00

...RARB, RASSF1, SCGB3A1, CCND2 (P < 0.0001), with an area under the ROC curve varying between 0.89 (95 % CI 0.82-0.97) and...

Nuclear receptor corepressors Ncor1 and Ncor2 (Smrt) are required for retinoic …

Kumar(Sandeep),Cunningham(Thomas J),Duester(… Dev Biol 0000-00-00

...Rarb that is activated by RA. CRISPR/Cas9-mediated genomic deletion of the Fgf8 RARE in mouse embryos often resulted in ...

Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressi…

Srour(Myriam),Caron(Véronique),Pearson(Toni)… Hum Mutat 0000-00-00

...RARB) gene cause microphthalmia and diaphragmatic hernia. However, the natural history of affected subjects beyond the p...

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