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A schematic representation of 24 ABCC8 missense SNPs in the protein ...
Schematic of the biochemical mechanism of KCNJ11 and ABCC8 genes in ...
ABCC8 and KNJ11 genes and their encoded proteins and functions. The ...
Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated ...
Genetic variants of ABCC8 and clinical manifestations in eight Chinese ...
Summary of Abcc8 gene regulation in central nervous system (CNS ...
Gene Q09428 | Protein ABCC8 - Overview | canSAR.ai
Identification of an ABCC8 variant in a kindred with transient ...
Full article: Genome-edited zebrafish model of ABCC8 loss-of-function ...
Schematic view of chromosome 11 where the KCNJ11 and ABCC8 genes are ...
Transient diabetes mellitus with ABCC8 variant successfully treated ...
Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension ...
Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus ...
Diabetes and ABCC8 Mutations in Nine Families with Neonatal Diabetes ...
ABCC8 mutation decreased the insulin secretion rate in low and high ...
Neonatal hyperinsulinism with an ABCC8 mutation: A case report
The genetic variants in ABCC8 exons identified in our patients, their ...
Gene Q09428 | Protein ABCC8 - Interaction network | canSAR.ai
Abcc8 mRNA and SUR1 protein are upregulated in cortex adjacent to SAH ...
Panel A: Silencing of ABCC8 with siRNA duplexes protects T98G cells ...
BIOCELL | Free Full-Text | ABCC8 is correlated with immune cell ...
ABCC8 - Wikipedia
Transcriptional stimulation of the Abcc8 promoter by hypoxia and by ...
Frontiers | Case report: Congenital hyperinsulinemia with ABCC8 gene ...
ABCC8 Gene - GeneCards | ABCC8 Protein | ABCC8 Antibody
Polymerase chain reaction-direct sequencing analysis of the ABCC8 gene ...
Clinical and Genetic Characteristics of ABCC8 Nonneonatal Diabetes ...
Analysis of ABCC8 mRNA expression according to gender, age ...
(a) Family with activating ABCC8 R1380C mutation. Diabetes (closed ...
Main characteristics of the adult carriers of an ABCC8 mutation ...
Tissue expression of ABCC8 - Staining in duodenum - The Human Protein Atlas
Analysis of ABCC8 mRNA expression according to IDH mutation and 1p/19q ...
Figure1: Sanger sequencing of ABCC8 gene in the proband and his ...
Identification of heterozygous mutations of ABCC8 gene responsible for ...
Targeted mutagenesis of the murine Abcc8 gene and production of the ...
Association of ABCC8 C/T genotypes in participants based on risk models ...
Subcellular - ABCC8 - The Human Protein Atlas
A novel mutation of ABCC8 gene in a patient with diazoxide-unresponsive ...
Tissue expression of ABCC8 - Staining in pancreas - The Human Protein Atlas
ABCC8 mutation. (A) The patient had a G→T nucleotide change at position ...
Upregulation of Abcc8 and Trpm4 mRNA in TLR4-activated rat microglia in ...
Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH ...
ABCC8 Monoclonal Antibody (3E1) | Invitrogen (H00006833-M02)
Figure 3 from Co-inheritance of two ABCC8 mutations causing an ...
Congenital Hyperinsulinism Caused by a De Novo Mutation in the ABCC8 ...
Regionally clustered ABCC8 polymorphisms in a prospective cohort ...
(PDF) Genetic variants of ABCC8 and clinical manifestations in eight ...
An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered ...
ABCC8 gene c.2506C>T mutated sequence in the proband. Arrows indicate ...
AS-ODN targeting Abcc8 and Trpm4, but not Kcnj11, reduces hemorrhagic ...
Permanent neonatal diabetes due to activating mutations in ABCC8 and ...
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal ...
(PDF) Neonatal hyperinsulinism with an ABCC8 mutation: A case report
Dominantly acting ABCC8 mutations in patients with medically ...
ABCC8 - Antibodies - The Human Protein Atlas
SOLUTION: Generation of an abcc8 heterozygous mutation human embryonic ...
(PDF) Identification of heterozygous mutations of ABCC8 gene ...
Figure 1 from Co-inheritance of two ABCC8 mutations causing an ...
Splicing in silico analysis of the variants detected in the ABCC8 gene ...
Pancreas of infant with CHI and paternal ABCC8 showing nucleomegaly ...
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ...
ABCC8 Single Nucleotide Polymorphisms are associated with Cerebral ...
Effect of Abcc8 knockout (KO) on axial diffusivity (AD) in brain after ...
Identification of ABCC8 as a contributory gene to impaired early-phase ...
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ ...
abcC8⁻ cells have streaming defects and have impaired cAMP release from ...
Frontiers | Integration of genomic analysis and transcript expression ...
Identification and rescue of congenital hyperinsulinism-associated ...
Type 2 diabetes pathogenesis | PPTX
Representative immunohistochemical images of different ABCCs family ...
Variants identified in ABCC8. ID and etiology of patients in which a ...
Increased ATPase activity produced by mutations at arginine-1380 in ...
Figure 2 from Molecular mechanisms of congenital hyperinsulinism due to ...
Results of genetic analysis (ABCC8 mutations). | Download Scientific ...
Fig. 1
Schematic diagram of the locations of 13 mutations identified in the ...
Association between antidiabetic drug targets and psychiatric disorders ...
Targeting SUR1/Abcc8-Type Neuroendocrine KATP Channels in Pancreatic ...
Congenital hyperinsulinemic hypoglycaemia in a neonate: a rare ...
(PDF) Congenital hyperinsulinism: clinical and molecular ...
Glibenclamide and Abcc8−/− protect against axonal damage. a-d White ...
Update of variants identified in the pancreatic β‐cell KATP channel ...
Glibenclamide and Abcc8−/− suppress immune cell infiltration in EAE ...
CRISPR-based genome editing in primary human pancreatic islet cells - PMC
Glibenclamide and Abcc8−/− promote remyelination in EAE. a-d White ...
