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searching for ATP7A 8 found (28 total)

alternate case: aTP7A

Trichoptilosis (207 words) [view diff] exact match in snippet view article find links to article

Dictionary, Pocket edition, 21st edition, 1968. Kaler, Stephen G (May 9, 2003). ATP7A-Related Copper Transport Disorders. National Center for Biotechnology Information

DCTN4 (346 words) [view diff] exact match in snippet view article find links to article

interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A". The Journal of Biological Chemistry. 281 (20): 14006–14. doi:10.1074/jbc

List of genes mutated in cutaneous conditions (108 words) [view diff] exact match in snippet view article find links to article

disease Acrokeratosis verruciformis of Hopf ATP2C1 Hailey–Hailey disease ATP7A Menkes kinky hair syndrome Occipital horn syndrome Cutis laxa ATP7B Wilson's

PDZD11 (691 words) [view diff] exact match in snippet view article find links to article

"A single PDZ domain protein interacts with the Menkes copper ATPase, ATP7A. A new protein implicated in copper homeostasis". J. Biol. Chem. 280 (39):

CCS (gene) (1,421 words) [view diff] exact match in snippet view article

increased expression of Cu binding proteins, namely, MT-I, MT-II, ATOX1, COX17, ATP7A to, presumably, reduce the amount of free Cu. Cells with CCS mutants have

WASHC2C (897 words) [view diff] exact match in snippet view article find links to article

WASH complex and regulates endosomal trafficking of the copper transporter ATP7A". Molecular Biology of the Cell. 26 (1): 91–103. doi:10.1091/mbc.E14-06-1073

MicroRNA 495 (761 words) [view diff] exact match in snippet view article find links to article

by modulation of copper-transporting P-type adenosine triphosphatase A (ATP7A)". J. Cell. Biochem. 115 (7): 1234–42. doi:10.1002/jcb.24665. PMID 24038379

Pili torti (4,454 words) [view diff] exact match in snippet view article find links to article

Laurent; Moraine, Claude (1997). "A C2055T Transition in Exon 8 of the ATP7A Gene Is Associated with Exon Skipping in an Occipital Horn Syndrome Family"