DNAJC12 Gene - GeneCards | DJC12 Protein | DJC12 Antibody
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
![Recombinant Anti-DNAJC12 antibody [EPR10067] (ab167425) | Abcam](https://www.abcam.com/ps/products/167/ab167425/Images/ab167425-165907-anti-dnajc12-antibody-epr10067-western-blot.jpg "Recombinant Anti-DNAJC12 antibody [EPR10067] (ab167425) | Abcam")
Recombinant Anti-DNAJC12 antibody [EPR10067] (ab167425) | Abcam
Effect of DNAJC12 overexpression on expression of various genes. (A)... | Download Scientific Diagram
Elliott's Journey with DNAJC12 Deficiency - Rare Disease Day 2023
Abnova™ DNAJC12 Recombinant Protein 10μg Abnova™ DNAJC12 Recombinant Protein | Fisher Scientific
pENTR223-DNAJC12-T19C plasmid,pENTR223-DNAJC12-T19C,pENTR223-DNAJC12-T19C plasmid,pENTR223-DNAJC12-T19C sequence,pENTR223-DNAJC12-T19C map
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar
Gene: DNAJC12 (ENSG00000108176) - Summary - Homo_sapiens - Ensembl genome browser 110
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemias - ScienceDirect
DNAJC12 and dopa‐responsive nonprogressive parkinsonism - Straniero - 2017 - Annals of Neurology - Wiley Online Library
Proponen incluir un gen recientemente descrito en el cribado neonatal de la hiperfenilalaninemia | CIBERER
Two novel mutations in DNAJC12 identified by whole‐exome sequencing in a patient with mild hyperphenylalaninemia - Li - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
DNAJC12 promotes lung cancer growth by regulating the activation of β‑catenin
dNAJc12 expression levels are upregulated in human lung cancer tissues.... | Download Scientific Diagram
DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis | European Journal of Human Genetics
Chapter 22 – Neurotransmitter Disorders: DNAJC12-Deficient Hyperphenylalaninemia – An Emerging Neurotransmitter Disorder | Neupsy Key
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar
DnaJ/HSP40 Homolog Subfamily C, Member 12 (DNAJC12) Protein | Abbexa Ltd
DNAJC12 Gene - GeneCards | DJC12 Protein | DJC12 Antibody
DNAJC12 Antibody (NBP1-57718): Novus Biologicals
