Results 211 to 220 of about 9,634,082 (235)
Cholinergic Augmentation of Insulin Release Requires Ankyrin-B
The scaffolding protein ankyrin-B is needed for maximal insulin release, and loss of function is a risk factor for diabetes.
Jane A, Healy +10 more
openaire +3 more sources
Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development
Variants in the ANK3 gene encoding ankyrin-G are associated with neurodevelopmental disorders, including intellectual disability, autism, schizophrenia, and bipolar disorder. However, no upstream regulators of ankyrin-G at synapses are known.
Sehyoun Yoon +2 more
exaly +3 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
119-OR: Ankyrin-B Modulates Lipid Metabolism in Brown Adipocytes
Diabetes, 2021Human variants in the membrane adaptor ankyrin-B (AnkB) present at frequencies from 0.05 to 7% across different ethnicities have been linked to obesity and type 2 diabetes (T2D). We reported that knock-in mice bearing T2D-linked human AnkB variants develop age- or diet-dependent obesity and insulin resistance (IR).
ASHLEY AGUILLARD +2 more
openaire +1 more source
Ankyrin-B structurally defines terminal microdomains of peripheral somatosensory axons
Brain Structure and Function, 2012Axons are subdivided into functionally organized microdomains, which are required for generation and propagation of action potentials (APs). In the central nervous system (CNS), APs are generated near the soma in the axon initial segment (AIS) and propagated by nodes of Ranvier (noR).
Maren, Engelhardt +4 more
openaire +2 more sources
Regulation of Pancreatic Beta Cell Function by Ankyrin‐B
The FASEB Journal, 2017Functional variants of the cytoskeletal protein ankyrin‐B (AnkB) have been implicated in human hereditary cardiac arrhythmia and type 2 diabetes (T2D).1–3 We recently showed that knock‐in mice expressing human AnkB variants p.R1788W (present in 0.2% Caucasians and associated with T2D) or p.L1622I (present in 7.5% of African ...
Damaris N Lorenzo +2 more
openaire +1 more source
Pancreatology, 2010
In spite of the increasing knowledge of the molecular pathology of pancreatic ductal adenocarcinoma (PDAC), treatment of this tumor still remains an unresolved problem. Thus, the identification of 'novel' genes involved in pancreatic tumor progression is essential for early diagnosis and new treatment regimens of PDAC.
Ying, Chen +2 more
openaire +2 more sources
In spite of the increasing knowledge of the molecular pathology of pancreatic ductal adenocarcinoma (PDAC), treatment of this tumor still remains an unresolved problem. Thus, the identification of 'novel' genes involved in pancreatic tumor progression is essential for early diagnosis and new treatment regimens of PDAC.
Ying, Chen +2 more
openaire +2 more sources
Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation
2015Ankyrins are a family of scaffold proteins, which serves to link great varieties of functional related but structurally diverse integral membrane proteins to the spectrin-based cytoskeletons. In vertebrates, the Ankyrin family consists of three members: ankyrin-R (AnkR), ankyrin-B (AnkB) and ankyrin-G (AnkG), encoded by ANK1, ANK2 and ANK3 ...
openaire +2 more sources
Analysis of ankyrin-B gene mutations in patients with long QT syndrome.
Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2008To identify the ankyrin-B gene mutations that cause long QT syndrome (LQTS) and determine the prevalence of such mutations in Japanese patients with LQTS.We conducted a search for ankyrin-B gene mutation in 78 unrelated patients with LQTS (28 males and 50 females, aged 2 to 89 years).
Xiang, Zhou +12 more
openaire +1 more source
Sequence and Structure-Based Analyses of Human Ankyrin Repeats
Molecules, 2022Broto Chakrabarty +2 more
exaly
Identification of novel intracellular mechanisms in developmental spine pruning through Ankyrin B.
2019Dendritic spines are the predominant site of glutamatergic inputs throughout the brain. Regulation of spines is therefore critical for refining cortical networks. This research sought to define mechanisms for determining spine fate during developmental synapse remodeling.
openaire +1 more source

