Papers associated with muscle (and slc7a5)

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	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5., Espinoza-Lewis RA., Dev Biol. March 15, 2009; 327 (2): 376-85.
	Functional characterization of two S-nitroso-L-cysteine transporters, which mediate movement of NO equivalents into vascular cells., Li S., Am J Physiol Cell Physiol. April 1, 2007; 292 (4): C1263-71.
	Spatial and temporal expression of the Grainyhead-like transcription factor family during murine development., Auden A., Gene Expr Patterns. October 1, 2006; 6 (8): 964-70.
	Transcriptional regulation of the cardiac-specific MLC2 gene during Xenopus embryonic development., Latinkic BV., Development. February 1, 2004; 131 (3): 669-79.
	SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family., Bassi MT., Genomics. December 1, 1999; 62 (2): 297-303.
	Identification of a membrane protein, LAT-2, that Co-expresses with 4F2 heavy chain, an L-type amino acid transport activity with broad specificity for small and large zwitterionic amino acids., Pineda M., J Biol Chem. July 9, 1999; 274 (28): 19738-44.
	Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene., Torrents D., Nat Genet. March 1, 1999; 21 (3): 293-6.

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