wd

Also found in: Medical, Financial, Encyclopedia.
(redirected from ATP7B)

wd

abbreviation for
1. ward
2. (Forestry) wood
3. (Linguistics) word

WD

abbreviation for
1. (Government, Politics & Diplomacy) War Department
2. (Government, Politics & Diplomacy) Works Department
3. (Automotive Engineering) (Windward Islands) Dominica (international car registration)
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

wd.

1. ward.
2. word.

W.D.

War Department.
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
Mentioned in
References in periodicals archive
View Report: https://www.transparencymarketresearch.com/wilsons-disease-market.html Individuals suffering from Wilson's disease are unable to discharge copper from the liver at a normal rate because of mutation in ATP7B gene.
Wilson's Disease Market Shares, Strategies and Forecasts, Analysis and Overview upto 2025
La enfermedad de Wilson es una entidad de caracter autosomico recesivo, causada por la mutacion del gen ATP7B que codifica una proteina del transportador intracelular de cobre (Cpx-tipo ATPasa) (50).
Trastornos psiquiatricos secundarios a enfermedades neurometabolicas
Copper taken up by hepatocyte CTR1 is delivered to ATP7B and CP CP facilitates iron loading onto TF by oxidation (Fe2+ Fe3+).
Copper Deficiency: Mimic of Myelodysplasia
Li et al., "Rescue of ATP7B function in hepatocyte-like cells from Wilson's disease induced pluripotent stem cells using gene therapy or the chaperone drug curcumin," Human Molecular Genetics, vol.
Current Perspectives Regarding Stem Cell-Based Therapy for Liver Cirrhosis
Spectrum and classification of ATP7B variants in a large cohort of Chinese patients with Wilson's disease guides genetic diagnosis.
A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient
ATP7B mediates vesicular sequestration of copper: Insight into biliary copper excretion.
Effects of graded levels of cupric citrate on growth performance, antioxidant status, serum lipid metabolites and immunity, and tissue residues of trace elements in weaned pigs
(Mutation R1319X in gene ATP7B and neurological form in Wilson's disease.
GEN-002: Mutacion R1319X en el gen ATP7B y presentacion neurologica de la Enfermedad de Wilson. Reporte de un caso
The basic pathophysiology relates to improper handling of copper by the liver owing to the dysfunctional ATP7B gene.
Suspected Wilson's disease presenting with normal serum ceruloplasmin levels
Alterations in the gene, which is responsible for the synthesis of protein P-type ATPase (ATP7B), lead to pathological copper accumulation, especially in the liver and the brain [2].
Study on Lesion Assessment of Cerebello-Thalamo-Cortical Network in Wilson's Disease with Diffusion Tensor Imaging
Copyright © 2003-2025 Farlex, Inc Disclaimer
All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.