Phenotype Variability in Patients Carrying KCNJ2 Mutations | Circulation: Cardiovascular Genetics
Overexpression of KCNJ2 in induced pluripotent stem cell-derived cardiomyocytes for the assessment of QT-prolonging drugs - ScienceDirect
Mutations of KCNJ2 gene associated with Andersen–Tawil syndrome in Korean families | Journal of Human Genetics
Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome - Journal of the Neurological Sciences
The K+ channel KIR2.1 functions in tandem with proton influx to mediate sour taste transduction | PNAS
![Recombinant Anti-Kir2.1/KCNJ2 antibody [EPR4530] (ab109750) | Abcam](https://www.abcam.com/ps/products/109/ab109750/Images/ab109750-122746-anti-kir21-antibody-epr4530-western-blot.jpg "Recombinant Anti-Kir2.1/KCNJ2 antibody [EPR4530] (ab109750) | Abcam")
Recombinant Anti-Kir2.1/KCNJ2 antibody [EPR4530] (ab109750) | Abcam
Anti-KIR2.1 KCNJ2 Antibody
Biophysical and Molecular Characterization of a Novel De Novo KCNJ2 Mutation Associated With Andersen-Tawil Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia Mimicry | Circulation: Cardiovascular Genetics
KCNJ2 mutations in arrhythmia patients referred for LQT testing: A mutation T305A with novel effect on rectification properties - Heart Rhythm
Relative mRNA levels of (A) Kcnj2 (Kir2.1), (B) Kcnj3 (Kir3.1), and (C)... | Download Scientific Diagram
Computational prediction of the effect of D172N KCNJ2 mutation on ventricular pumping during sinus rhythm and reentry | SpringerLink
Atrial arrhythmogenicity of KCNJ2 mutations in short QT syndrome: Insights from virtual human atria | PLOS Computational Biology
KCNJ2 Gene - GeneCards | KCNJ2 Protein | KCNJ2 Antibody
Functional dissection of the Sox9–Kcnj2 locus identifies nonessential and instructive roles of TAD architecture | Nature Genetics
Proposed arrhythmia mechanism for KCNJ2 mutation: adrenergic loss of I... | Download Scientific Diagram
Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2‐associated Andersen–Tawil Syndrome - Adams - 2016 - The Journal of Physiology - Wiley Online Library
Upregulation of the inwardly rectifying potassium channel Kir2.1 (KCNJ2) modulates multidrug resistance of small-cell lung cancer under the regulation of miR-7 and the Ras/MAPK pathway | Molecular Cancer | Full Text
Functional characterization of KCNJ2 mutations associated with Andersen-Tawil syndrome and atrial tachycardia
Upregulation of the inwardly rectifying potassium channel Kir2.1 (KCNJ2) modulates multidrug resistance of small-cell lung cancer under the regulation of miR-7 and the Ras/MAPK pathway | Molecular Cancer | Full Text
Mutation detection by sequence analysis of the KCNJ2 coding region. (A)... | Download Scientific Diagram
Kir2.1 (KCNJ2) Guinea Pig anti-Human, Mouse, Rat, Unconjugated, Polyclonal, Invitrogen™ 50 μL; Unconjugated Products | Fisher Scientific
KCNJ2 Antibody | FabGennix
Identification of novel KCNJ2 gene mutation p.Thr142Pro (c.424A>C) in... | Download Scientific Diagram
Kir2.1 (KCNJ2) Antibody (PA5-88883)
Multiple Promoter Elements Interact to Control the Transcription of the Potassium Channel Gene, KCNJ2 * - Journal of Biological Chemistry
Overexpression of KCNJ2 in induced pluripotent stem cell-derived cardiomyocytes for the assessment of QT-prolonging drugs - ScienceDirect
