Atp7b And Autism

Involvement of Protein Kinase D in Expression and Trafficking of ATP7B

Epidemiology of Wilsons Disease and Pathogenic Variants of the ATP7B

ATP7A and ATP7B copper transporters have distinct functions in the

Spectrum of Pathogenic Variants of the ATP7B Gene and Genotype

ATP7A and ATP7B copper transporters have distinct functions in the

Epidemiology of Wilsons Disease and Pathogenic Variants of the ATP7B

ATP7A and ATP7B copper transporters have distinct functions in the

Frontiers Role of the PType ATPases ATP7A and ATP7B in brain copper

Functional Interactions of CuATPase ATP7B with Cisplatin and the Role

Frontiers Role of the PType ATPases ATP7A and ATP7B in brain copper

ATP7A and ATP7B copper transporters have distinct functions in the

Spectrum of Pathogenic Variants of the ATP7B Gene and Genotype

ATP7A and ATP7B copper transporters have distinct functions in the

Functional Interactions of CuATPase ATP7B with Cisplatin and the Role

ATP7A and ATP7B copper transporters have distinct functions in the

Spectrum of Pathogenic Variants of the ATP7B Gene and Genotype

Involvement of Protein Kinase D in Expression and Trafficking of ATP7B

Direct Interaction of ATP7B and LC3B Proteins Suggests a Cooperative

Functional Interactions of CuATPase ATP7B with Cisplatin and the Role

Evidence for synergistic effects of PRNP and ATP7B mutations in severe

The Loop Connecting MetalBinding Domains 3 and 4 of ATP7B Is a Target

人 ATP7B 基因中的单核苷酸多态性会改变 ATP7B 蛋白的特性。,Metallomics - X-MOL

ATP7B ATP7B Metallomics XMOL

ATP7B R778L mutant hepatocytes resist copper toxicity by activating

ATP7b Antibody

Human copper transporter ATP7B Wilson disease protein forms stable

Navigating the CRISPRCas Landscape for Enhanced Diagnosis and

Frontiers The interplay between copper metabolism and microbes in

Fulllength ATP7B reconstituted through protein transsplicing corrects

Direct Measurement of ATP7B Peptides Is Highly Effective in the

TFEB Regulates ATP7B Expression to Promote Platinum Chemoresistance in

Copper directs ATP7B to the apical domain of hepatic cells via

Navigating the CRISPRCas Landscape for Enhanced Diagnosis and

Frontiers Functional Characterization of Novel ATP7B Variants for

Atp7b HU Taconic Biosciences

TFEB Regulates ATP7B Expression to Promote Platinum Chemoresistance in

Direct Measurement of ATP7B Peptides Is Highly Effective in the

Functional Properties of the Coppertransporting ATPase ATP7B The

Copper directs ATP7B to the apical domain of hepatic cells via

ATP7b Antibody BSA Free NB100360 by Novus Part of BioTechne

Copper directs ATP7B to the apical domain of hepatic cells via

Activity and Trafficking of CopperTransporting ATPases in Tumor

Copper directs ATP7B to the apical domain of hepatic cells via

Systematic Analysis and Insights Into the Mutation Spectrum and Ethnic

ATP7B Ab

A glimpse into the regulation of the Wilson disease protein ATP7B

Homozygous frame shift variant in ATP7B exon 1 leads to bypass of

Identification of mutations in the ATP7B gene in 14 Wilson disease

Functional Characterization of Novel ATP7B Variants for Diagnosis of

Distinct Wilsondisease mutations in ATP7B are associated with enhanced

Genetic analysis of ATP7B in 102 south Indian families with Wilson

Dysfunction of ATP7B Splicing Variant Caused by Enhanced Interaction

Distinct Wilsondisease mutations in ATP7B are associated with enhanced

Systemic deletion of Atp7b modifies the hepatocytes response to copper

Diverse Functional Properties of Wilson Disease ATP7B Variants

TFEB Regulates ATP7B Expression to Promote Platinum Chemoresistance in

Novel compound heterozygote mutations in the ATP7B gene in an Iranian

Schematic representation of human ATP7B on the basis of Download

ATP7B Antibody

Fulllength ATP7B reconstituted through protein transsplicing corrects

Distinct Wilsondisease mutations in ATP7B are associated with enhanced

Structures of the human Wilson disease copper transporter ATP7BCell

威尔逊病蛋白ATP7B的调控一瞥，揭示了哺乳动物根尖运输途径的复杂性,Metallomics - X-MOL

ATP7BMetallomics XMOL

lipoprotein

基础医学院夏梦/王青青团队在 PNAS发文揭示帕金森病致病基因ATP13A2调节神经炎症的新机制

PNASATP13A2

ATF6β 缺乏会在压力条件下引发类似焦虑的行为和多动症,Neurochemical Research - X-MOL

ATF6 Neurochemical Research XMOL

ATP7AATP7A Rabbit pAb ATP7A

兔抗ATP7A 多克隆抗体,Anti-ATP7A rabbit polyclonal antibody 生命科学产品与技术服务-生工生物工程 ...

ATP7A AntiATP7A rabbit polyclonal antibody

Frontiers The role of copper dysregulation in Wilson disease an

The metal chaperone Atox1 regulates the activity of the human copper

ATP7BDeficient Hepatocytes Reveal the Importance of Protein Misfolding

Membrane Trafficking Lab

AP-1γ2 is an adaptor protein 1 variant required for endosome-to-Golgi ...

AP12 is an adaptor protein 1 variant required for endosometoGolgi

Oncology Letters

ATP7B

Oncology Letters

Metabolic dysregulation in the Atp7b Wilsons disease mouse model PNAS

Case of EarlyOnset Parkinsons Disease in a Heterozygous Mutation

Frontiers Silent but significant Functional elucidation of a

ATP7BDeficient Hepatocytes Reveal the Importance of Protein Misfolding

Oncology Letters

ATP7bEPR6794 ab124973 Abcam

Oxysterol misbalance critically contributes to Wilson disease

Frontiers Silent but significant Functional elucidation of a

ATP7BDeficient Hepatocytes Reveal the Importance of Protein Misfolding

International Journal of Molecular Medicine

BOSTER Biological Technology coltd 19932026

AntiATP7b Rabbit mAb 40T68P68

Mol Psychiatry：冯杜团队发现ATP9A是ADHD和ID的全新致病基因

Mol PsychiatryATP9AADHDID

AntiATP7b Rabbit mAb 40T68P68

Mol PsychiatryATP9AADHDID

ActRII

ATP ATP7B MCE

ATG7 Ab

Atp7bdependent choroid plexus dysfunction causes transient copper

Translocation of Platinum Anticancer Drugs by Human Copper ATPases

ATP7BDeficient Hepatocytes Reveal the Importance of Protein Misfolding

Clusterin Apolipoprotein J a Molecular Chaperone That Facilitates

Structures of the human Wilson disease copper transporter ATP7B Cell

Intracellular targeting of coppertransporting ATPase ATP7A in a normal

Atp7bdependent choroid plexus dysfunction causes transient copper

ATP7B ELISAatp7bCSDN

Wilsons

ATP7B

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