Voltage-gated Cav1 channels in disorders of vision and hearing

MA Joiner, A Lee - Current molecular pharmacology, 2015 - ingentaconnect.com
Cav1 channels mediate L-type Ca2+ currents that trigger the exocytotic release of glutamate
from the specialized “ribbon” synapse of retinal photoreceptors (PRs) and cochlear inner …

Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients

H Nawaz, A Parveen, SA Khan, AK Zalan, MA Khan… - Heliyon, 2024 - cell.com
Brachyolmia is a heterogeneous group of developmental disorders characterized by a short
trunk, short stature, scoliosis, and generalized platyspondyly without significant deformities …

Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1. 2 L-type Ca2+ channels by calmodulin and Ca2+-binding protein 1

S Oz, A Benmocha, Y Sasson, D Sachyani… - Journal of Biological …, 2013 - ASBMB
Ca V 1.2 interacts with the Ca 2+ sensor proteins, calmodulin (CaM) and calcium-binding
protein 1 (CaBP1), via multiple, partially overlapping sites in the main subunit of Ca V 1.2, α …

Localization and expression of CaBP1/caldendrin in the mouse brain

KY Kim, ES Scholl, X Liu, A Shepherd, F Haeseleer… - Neuroscience, 2014 - Elsevier
Abstract Ca 2+ binding protein 1 (CaBP1) and caldendrin are alternatively spliced variants
of a subfamily of CaBPs with high homology to calmodulin. Although CaBP1 and caldendrin …

Expression and Localization of CaBP Ca2+ Binding Proteins in the Mouse Cochlea

T Yang, ES Scholl, N Pan, B Fritzsch, F Haeseleer… - PloS one, 2016 - journals.plos.org
CaBPs are a family of EF-hand Ca2+ binding proteins that are structurally similar to
calmodulin. CaBPs can interact with, and yet differentially modulate, effectors that are …

Functions of CaBP1 and CaBP2 in the peripheral auditory system

T Yang, N Hu, T Pangršič, S Green, M Hansen, A Lee - Hearing research, 2018 - Elsevier
CaBPs are a family of Ca 2+ binding proteins related to calmodulin. Two CaBP family
members, CaBP1 and CaBP2, are highly expressed in the cochlea. Here, we investigated …

Molecular parallelism in fast-twitch muscle proteins in echolocating mammals

JH Lee, KM Lewis, TW Moural, B Kirilenko… - Science …, 2018 - science.org
Detecting associations between genomic changes and phenotypic differences is
fundamental to understanding how phenotypes evolved. By systematically screening for …

Voltage-gated calcium channels (CaV) in GtoPdb v.2023.1

WA Catterall, E Perez-Reyes, TP Snutch… - IUPHAR/BPS Guide …, 2023 - journals.ed.ac.uk
Ca 2+ channels are voltage-gated ion channels present in the membrane of most excitable
cells. The nomenclature for Ca 2+ channels was proposed by [131] and approved by the NC …

ARNSHL gene identification: past, present and future

A Imtiaz - Molecular Genetics and Genomics, 2022 - Springer
Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary
deafness. It is genetically highly heterogeneous and about 89 gene loci and 76 gene's …

Decalmodulation of Cav1 channels by CaBPs

J Hardie, A Lee - Channels, 2016 - Taylor & Francis
Ca2+-dependent inactivation (CDI) is a negative feedback regulation of voltage-gated Cav1
and Cav2 channels that is mediated by the Ca2+ sensing protein, calmodulin (CaM) …