Results 101 to 110 of about 3,079 (182)

Author Correction: Long non-coding RNA NR2F1-AS1 induces breast cancer lung metastatic dormancy by regulating NR2F1 and ΔNp63 [PDF]

Nature Communications, 2021
Yingjie Liu, Peiyuan Zhang, Qiuyao Wu, Houqin Fang, Yuan Wang, Yansen Xiao, Min Cong, Tingting Wang, Yunfei He, Chengxin Ma, Pu Tian, Yajun Liang, Lun-Xiu Qin, Qingcheng Yang, Qifeng Yang, Lujian Liao, Guohong Hu   +16 more
openaire   +2 more sources

Overview of the NR2F1 subnetwork inference task.

, 2019
The first panel displays a background network composed of the source NR2F1 (black), target DE genes (blue), and interactions (dashed and solid lines). Transcription factors are identified as bright magenta nodes.
Michael Gould (542219), Eunju Park (1463329), Mark Craven (51222), Amanda Henning (6889304), Hoifung Poon (4096399), Paul Ahlquist (78214), Sid Kiblawi (6889301), Deborah Chasman (569731)   +7 more
core   +1 more source

DataSheet_1_METTL3 inhibits inflammation of retinal pigment epithelium cells by regulating NR2F1 in an m6A-dependent manner.docx

, 2022
N6-metyladenosine (m6A) RNA methylation has been proven to be involved in diverse biological processes, but its potential roles in the development of lipopolysaccharide (LPS) induced retinal pigment epithelium (RPE) inflammation have not been revealed ...
Na Li (6550), Jiayu Meng (13131456), Chenyang Zhao (533763), Xianyang Liu (13131459), Yusen Liu (234074), Shengping Hou (231471), Shiyun Tang (3755674), Qian Zhou (125859)   +7 more
core   +1 more source

Klf9 is a downstream inner ear target of NR2F1.

, 2013
Klf9 expression is significantly up-regulated in Nr2f1–/– (KO) inner ear but not in the cerebral cortex, as determined by qRT-PCR.
Fernanda R. Ruiz (492231), Na Li (6550), Fred A. Pereira (254120), David W. Cuthbertson (492230), David Y. Chiang (389033)   +4 more
core   +1 more source

Synteny analysis of Nr2f1/2/5/6 genes in cnidaria.

, 2021
Schematic of the loci flanking Nr2f1/2/5/6 gene duplications in cnidaria N. vectensis, A. millepora, and H vulgaris. Only the one H. vulgaris gene presently has available genomic information. Arrows indicate transcription orientation.
Ugo Coppola (3524945), Joshua S. Waxman (11740611)   +1 more
core   +1 more source

Reduced NR2F1 transcript levels in human breast cancer correlate with histological grade 3 tumors.

, 2013
A) Average (+/− sem) of the normalized median NR2F1 probe intensities, obtained from a total of 12 breast cancer expression studies (with 120+ samples each study) available through Oncomine.
Jill D. Haag (220668), Alexi A. Schoenborn (421293), Ann Tran (421292), Patricia A. Powers (421298), Christina Kendziorski (42423), Deepak Sharma (131639), Michael N. Gould (306367), Ning Leng (386645), Anna I. Rissman (421291), Mark R. Eichelberg (342238), David Q. Leinweber (421296), Dan S. Peiffer (421295), Matthew J. Muelbl (342240), Caroline M. Alexander (117364), Manorama C. John (421297), Bart M. G. Smits (342237), Amanda L. Meilahn (342239), Rachael C. Baird (421294)   +17 more
core   +1 more source

Nr2f1 Heterozygous Knockout Mice Recapitulate Neurological Phenotypes of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome and Show Impaired Hippocampal Synaptic Plasticity

, 2020
Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) has been identified as an autosomal-dominant disorder characterized by a complex neurological phenotype, with high prevalence of intellectual disability and optic nerve atrophy/hypoplasia.
Liu, Zhandong, Wang, Li, Schaaf, Christian P, Wang, Wei, Pereira, Fred A, Rech, Megan E, Zoghbi, Huda Y, Lopez, Joanna, Yin, Jiani, van der Heijden, Meike E, Seymour, Michelle L, Ruiz, Fernanda R, Wu, Samuel M, Raman, Ayush, Lewis, Richard A, Xia, Anping, Pedersen, Steen E, Pautler, Robia G, Chen, Chun-An   +18 more
core   +1 more source

Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome

EMBO Molecular Medicine, 2019
Optic nerve atrophy represents the most common form of hereditary optic neuropathies leading to vision impairment. The recently described Bosch‐Boonstra‐Schaaf optic atrophy (BBSOA) syndrome denotes an autosomal dominant genetic form of neuropathy caused
Michele Bertacchi, Agnès Gruart, Polynikis Kaimakis, Cécile Allet, Linda Serra, Paolo Giacobini, José M Delgado‐García, Paola Bovolenta, Michèle Studer   +8 more
doaj   +1 more source

Intersection of genes targeted by both NR2F1 and select miRNAs.

, 2013
(A) Identification of 107 genes by intersection of the 182 NR2F1 targets genes [12] with targets of the 11 miRNAs and (B) the percentage of these genes targeted by multiple miRNAs.
Fernanda R. Ruiz (492231), Na Li (6550), Fred A. Pereira (254120), David W. Cuthbertson (492230), David Y. Chiang (389033)   +4 more
core   +1 more source

Roles of the NR2F Family in the Development, Disease, and Cancer of the Lung

Journal of Developmental Biology
The NR2F family, including NR2F1, NR2F2, and NR2F6, belongs to the nuclear receptor superfamily. NR2F family members function as transcription factors and play essential roles in the development of multiple organs or tissues in mammals, including the ...
Jiaxin Yang, Wenjing Sun, Guizhong Cui
doaj   +1 more source