t/gene-abcc8

ABCC8 gene

Discuss publications and research concerning the ABCC8 gene.

0 members0 posts33 articles

Start the first discussion

Ask a question, share context or link a publication.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Causal association between antidiabetic drug targets and risk of Bell's palsy: A 2-sample Mendelian randomization study.
ABCC8
Expanding the genetic burden of low-evidence genes in pulmonary arterial hypertension.
ABCC8
Sarcopenia and chronic pain: Identification of shared genetic determinants and therapeutic implication.
ABCC8
Genetic and Clinical Characterisation of Congenital Hyperinsulinism: Identification of a Novel ABCC8 Variant.
ABCC8
Congenital Hyperinsulinemic Hypoglycemia With a New HADH Mutation and Pancreatic Overexpression of GLP-1 Receptors.
ABCC8
First diagnosis of familial partial lipodystrophy syndrome type 3 during pregnancy associated with a novel heterozygous PPARG variant and a concurrent ABCC8 variant: a case report.
ABCC8
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community.
ABCC8
Comprehensive Genetic Testing for Clinical Decision-Making in a Patient With Congenital Hyperinsulinism.
ABCC8
An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population.
ABCC8
Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes.
ABCC8

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details