Pages that link to "Q46047255"

The following pages link to Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters (Q46047255):

Displaying 43 items.

• Identification of zyklopen, a new member of the vertebrate multicopper ferroxidase family, and characterization in rodents and human cells (Q24294422) (← links)
• Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance (Q24642573) (← links)
• Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes (Q24647056) (← links)
• Deprivation of pantothenic acid elicits a movement disorder and azoospermia in a mouse model of pantothenate kinase-associated neurodegeneration (Q24684828) (← links)
• Transport of toxic metals by molecular mimicry (Q24812330) (← links)
• Mottled Mice and Non-Mammalian Models of Menkes Disease (Q26770905) (← links)
• Molecular genetics and pathophysiology of Menkes disease (Q28142471) (← links)
• Mislocalisation of hephaestin, a multicopper ferroxidase involved in basolateral intestinal iron transport, in the sex linked anaemia mouse (Q28238774) (← links)
• Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse (Q28297185) (← links)
• ATP7A-related copper transport diseases-emerging concepts and future trends (Q28302938) (← links)
• The copper transporter CTR1 provides an essential function in mammalian embryonic development (Q28366364) (← links)
• Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation (Q28505378) (← links)
• Effects of copper supplementation on copper absorption, tissue distribution, and copper transporter expression in an infant rat model (Q28573315) (← links)
• Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia (Q28588602) (← links)
• Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice (Q28594419) (← links)
• Regulation of copper transport crossing brain barrier systems by Cu-ATPases: effect of manganese exposure (Q29347141) (← links)
• Polarized sorting of the copper transporter ATP7B in neurons mediated by recognition of a dileucine signal by AP-1. (Q30615545) (← links)
• Diminution of toxic copper accumulation in toxic milk mice modeling Wilson disease by embryonic hepatocyte intrasplenic transplantation (Q33217543) (← links)
• ATP7B detoxifies silver in ciliated airway epithelial cells (Q33695461) (← links)
• A novel member of a zinc transporter family is defective in acrodermatitis enteropathica (Q34353666) (← links)
• The lumenal loop Met672-Pro707 of copper-transporting ATPase ATP7A binds metals and facilitates copper release from the intramembrane sites (Q35128218) (← links)
• Trace elements in human physiology and pathology. Copper (Q35598944) (← links)
• ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model (Q35623439) (← links)
• Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes (Q35870519) (← links)
• Biometals in rare neurodegenerative disorders of childhood. (Q36712834) (← links)
• Copper-transporting ATPases ATP7A and ATP7B: cousins, not twins (Q37000460) (← links)
• Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis (Q37112824) (← links)
• Copper transport protein (Ctr1) levels in mice are tissue specific and dependent on copper status (Q37283114) (← links)
• Copper handling machinery of the brain (Q37808945) (← links)
• Transendothelial Transport and Its Role in Therapeutics (Q38880426) (← links)
• Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin (Q39770874) (← links)
• Localization of the Wilson disease protein in murine intestine. (Q39955033) (← links)
• hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIA. (Q40781259) (← links)
• Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases. (Q40995220) (← links)
• Multiple transcripts coding for the menkes gene: evidence for alternative splicing of Menkes mRNA. (Q41019188) (← links)
• Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases (Q42671888) (← links)
• Dietary iron alters waterborne copper-induced gene expression in soft water acclimated zebrafish (Danio rerio). (Q46262207) (← links)
• Atp7a and Atp7b regulate copper homeostasis in developing male germ cells in mice. (Q47935607) (← links)
• A systems biology approach reveals new endoplasmic reticulum-associated targets for the correction of the ATP7B mutant causing Wilson disease. (Q48673647) (← links)
• Effect of the Mn oxidation state and lattice oxygen in Mn-based TiO2 catalysts on the low-temperature selective catalytic reduction of NO by NH3. (Q53359113) (← links)
• Somatic mosaicism in Menkes disease suggests choroid plexus‐mediated copper transport to the developing brain (Q55220574) (← links)
• Cerebrospinal Fluid-Directed rAAV9-rsATP7A Plus Subcutaneous Copper Histidinate Advance Survival and Outcomes in a Menkes Disease Mouse Model (Q59354904) (← links)
• Alterations in the expression of the Atp7a gene in the early postnatal development of the mosaic mutant mice (Atp7amo-ms) – An animal model for Menkes disease (Q85013328) (← links)