Showing 118 of 118on this page. Filters & sort apply to loaded results; URL updates for sharing.118 of 118 on this page
ABCC8 mutation decreased the insulin secretion rate in low and high ...
A novel mutation in the ABCC8 gene causing maturity-onset diabetes of ...
An image of Electropherogram sequencing a point mutation in the ABCC8 ...
The Growth History of a Girl carrying ABCC8 Gene Mutation resulting in ...
A case of transient neonatal diabetes due to a novel mutation in ABCC8 ...
Analysis of ABCC8 mRNA expression according to IDH mutation and 1p/19q ...
An example of the corresponding mutation in the KCNJ11 and ABCC8 genes ...
Loss of Function ABCC8 Mutations in Pulmonary Arterial Hypertension - PMC
Congenital Hyperinsulinism Caused by a De Novo Mutation in the ABCC8 ...
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal ...
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP ...
Regionally clustered ABCC8 polymorphisms in a prospective cohort ...
Schematic of the biochemical mechanism of KCNJ11 and ABCC8 genes in ...
Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension ...
Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated ...
Targeted mutagenesis of the murine Abcc8 gene and production of the ...
Permanent neonatal diabetes due to activating mutations in ABCC8 and ...
Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus ...
ABCC8 mutation. (A) The patient had a G→T nucleotide change at position ...
Genetic variants of ABCC8 and clinical manifestations in eight Chinese ...
Abnormal insulin secretion by KCNJ11 or ABCC8 activating mutations. An ...
Transient diabetes mellitus with ABCC8 variant successfully treated ...
(a) Family with activating ABCC8 R1380C mutation. Diabetes (closed ...
ABCC8 and KNJ11 genes and their encoded proteins and functions. The ...
A schematic representation of 24 ABCC8 missense SNPs in the protein ...
Neonatal diabetes caused by mutations in KCNJ11 or ABCC8 // Diabetes Genes
The genetic variants in ABCC8 exons identified in our patients, their ...
Neonatal hyperinsulinism with an ABCC8 mutation: A case report
Genome-edited zebrafish model of ABCC8 loss-of-function disease - PMC
Loss-Of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension ...
Summary of Abcc8 gene regulation in central nervous system (CNS ...
Pedigrees of children with HI harboring ABCC8 mutations. Pedigrees of ...
Identification of heterozygous mutations of ABCC8 gene responsible for ...
(PDF) Genome-edited zebrafish model of ABCC8 loss-of-function disease
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ ...
ABCC8 gene c.863G>A mutated sequence in the proband. Arrows indicate ...
Distribution of alterations in ABCC8 and ABCD2 genes. Top : The ...
Splicing in silico analysis of the variants detected in the ABCC8 gene ...
Identification of a compound heterozygous inactivating ABCC8 gene ...
Full article: Genome-edited zebrafish model of ABCC8 loss-of-function ...
Human ABCC8 cDNA Clones, HG17546 | Sino Biological
Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH ...
Figure 1 from Co-inheritance of two ABCC8 mutations causing an ...
Pedigree showing the inheritance of the R168C and S606T ABCC8 ...
ABCC8 and KCNJ11 gene mutations identified in 14 Korean patients with ...
(PDF) Identification of heterozygous mutations of ABCC8 gene ...
Locations of 160 KATP HI Mutations in ABCC8 and KCNJ11. Shown are the ...
BIOCELL | Free Full-Text | ABCC8 is correlated with immune cell ...
Relative Expression of a Dominant Mutated ABCC8 Allele Determines the ...
Diabetes and ABCC8 Mutations in Nine Families with Neonatal Diabetes ...
In situ hybridization shows upregulated Abcc8 mRNA in acute ischemic ...
Pedigree showing the inheritance of the novel Q54X ABCC8 mutation. The ...
Figure1: Sanger sequencing of ABCC8 gene in the proband and his ...
Partial pedigrees of families showing inheritance of KCNJ11 or ABCC8 ...
Overview of identified alterations in ABCC8 and ABCD2 genes in breast ...
ABCA8, ABCB4 and ABCC8 show distinctive SHH subtype associated ...
Frontiers | Case report: Congenital hyperinsulinemia with ABCC8 gene ...
Inheritance of a paternal ABCC8 variant and maternal loss of ...
Update of variants identified in the pancreatic β‐cell KATP channel ...
Experimental and Therapeutic Medicine
Figure 2 from Molecular mechanisms of congenital hyperinsulinism due to ...
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ...
Common mutations associated with CHI. (1) ATP gated K+ channel (KATP ...
Increased ATPase activity produced by mutations at arginine-1380 in ...
| Mutations of ABCC8, KLKB1, IL13RA2, ATRX, DAXX, and MEN1 in 98 ...
Identification and rescue of congenital hyperinsulinism-associated ...
Schematic diagram of the locations of 13 mutations identified in the ...
Multiple sequence alignment of ABCC8. Multiple sequence alignment of ...
Congenital hyperinsulinism: 2 case reports with different rare variants ...
Heterogeneous nature of diabetes in a family with a gain-of-function ...
CRISPR/Cas9 targeting of a non-coding variant in the ABCC8-KCNJ11 locus ...
Frontiers | Integration of genomic analysis and transcript expression ...
The genetic basis of congenital hyperinsulinism | Journal of Medical ...
Type 2 diabetes pathogenesis | PPTX
Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary ...
Figure 2 from Human Pancreas Endocrine Cell Populations and Activating ...
(PDF) Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ...
Congenital hyperinsulinemic hypoglycaemia in a neonate: a rare ...
Recognition of Sulfonylurea Receptor (ABCC8/9) Ligands by the Multidrug ...
ABCC8-Related Maturity-Onset Diabetes of the Young (MODY12): A Report ...
J of Diabetes Invest - 2013 - Takagi - Clinical and Functional ...
The eight variants have been shown on the three‐dimensional structure ...
Association between antidiabetic drug targets and psychiatric disorders ...
Genetic analysis revealed a heterozygote variation of c.4608G>A on exon ...
Journal of Diabetes: Vol 13, No 7
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein ...
(PDF) Molecular Mechanisms of Congenital Hyperinsulinism due to ...
Figure 5 from Molecular mechanisms of congenital hyperinsulinism due to ...
Results of genetic analysis (ABCC8 mutations). | Download Scientific ...
