Results 111 to 120 of about 1,143 (122)

Genome-wide association study of copy number variation and early growth traits in inner Mongolian cashmere goats. [PDF]

Front Vet Sci
Liu Y, Xi H, Xu Q, Zhou B, Li J, Su R, Lv Q, Zhang Y, Wang R, Wang Z.   +9 more
europepmc   +1 more source

The sticky business of Alphavirus capsid-host interactions. [PDF]

Trends Microbiol
Martin CK, Yin P, Kielian M.
europepmc   +1 more source

PRMT5-mediated arginine methylation of FXR1 is essential for RNA binding in cancer cells. [PDF]

Nucleic Acids Res
Vijayakumar A, Majumder M, Yin S, Brobbey C, Karam J, Howley B, Howe PH, Berto S, Madan LK, Gan W, Palanisamy V.   +10 more
europepmc   +1 more source

Molecular Mechanisms and Clinical Implications of Noncoding RNAs in Cancer. [PDF]

Noncoding RNA
Wang J, He X, Corpe C.
europepmc   +1 more source

Mechanistic insights into adipose-derived stem cells and exosomes in ischemia-reperfusion injury repair: from shared pathways to organ-specific therapeutics. [PDF]

Front Cell Dev Biol
Si J, Wang J, Dai H, Lv T, Zhao S, Chen W, Li L, Ding S, He Y.   +8 more
europepmc   +1 more source

The FXR1 network acts as a signaling scaffold for actomyosin remodeling. [PDF]

Cell
Chen X, Fansler MM, Janjoš U, Ule J, Mayr C.   +4 more
europepmc   +1 more source

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5-Methylcytosine-Modified circRNA-CCNL2 Regulates Vascular Remdeling in Hypoxic Pulmonary Hypertension Through Binding to FXR2

International Journal of Biological Macromolecules
Pulmonary hypertension (PH) is a malignant cardiovascular disease with a complex etiology. 5-Methylcytosine (m5C) is a post-transcriptional RNA modification identified in both stable and highly abundant RNAs, with a lower frequency of occurrence in circular RNAs (circRNAs).
June Bai, Hanliang Sun, Xinyue Song
exaly   +3 more sources

Expression of Three Zebrafish Orthologs of Human FMR1-Related Genes and Their Phylogenetic Relationships

Development Genes and Evolution, 2004
The original publication can be found at www.springerlink.comThe human fragile X mental retardation syndrome is caused by expansions of a CGG repeat in the FMR1 gene. FXR1 and FXR2 are autosomal paralogs of FMR1.
Michael Lardelli, Robert Ian Richards
exaly   +2 more sources

Loss of FXR1 and FXR2 promotes accumulation of TDP-43 in aging-related stress granules

Abstract Cytoplasmic mislocalization and aggregation of the RNA-binding protein TDP-43 in vulnerable neurons may accompany the primary neuropathology of various neurodegenerative diseases, or represent the hallmark of others, such as amyotrophic lateral sclerosis.
Sonja Menge, Lorena Decker, Karin M. Danzer, Patrick Oeckl, Axel Freischmidt   +4 more
openaire   +1 more source

NF-Y, AP2, Nrf1 and Sp1 Regulate the Fragile X-Related Gene 2 (FXR2)

Biochemical Journal, 2006
Karen Usdin
exaly