[HTML][HTML] The SLC9A-C mammalian Na+/H+ exchanger family: molecules, mechanisms, and physiology

SF Pedersen, L Counillon - Physiological reviews, 2019 - journals.physiology.org
Na+/H+ exchangers play pivotal roles in the control of cell and tissue pH by mediating the
electroneutral exchange of Na+ and H+ across cellular membranes. They belong to an …

SLC9/NHE gene family, a plasma membrane and organellar family of Na+/H+ exchangers

M Donowitz, CM Tse, D Fuster - Molecular aspects of medicine, 2013 - Elsevier
This brief review of the human Na/H exchanger gene family introduces a new classification
with three subgroups to the SLC9 gene family. Progress in the structure and function of this …

Traditional and emerging roles for the SLC9 Na+/H+ exchangers

DG Fuster, RT Alexander - Pflügers Archiv-European Journal of Physiology, 2014 - Springer
The SLC9 gene family encodes Na+/H+ exchangers (NHEs). These transmembrane
proteins transport ions across lipid bilayers in a diverse array of species from prokaryotes to …

An inside job: how endosomal Na+/H+ exchangers link to autism and neurological disease

KC Kondapalli, H Prasad, R Rao - Frontiers in cellular neuroscience, 2014 - frontiersin.org
Autism imposes a major impediment to childhood development and a huge emotional and
financial burden on society. In recent years, there has been rapidly accumulating genetic …

Sodium-Proton (Na+/H+) Antiporters: Properties and Roles in Health and Disease

E Padan, M Landau - The alkali metal ions: Their role for life, 2016 - Springer
The transmembranal Na+/H+ antiporters transport sodium (or several other monovalent
cations) in exchange for H+ across lipid bilayers in all kingdoms of life. They are critical in …

A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition

JY Garbern, M Neumann, JQ Trojanowski, VMY Lee… - Brain, 2010 - academic.oup.com
We have studied a family with severe mental retardation characterized by the virtual
absence of speech, autism spectrum disorder, epilepsy, late-onset ataxia, weakness and …

Functional evaluation of autism-associated mutations in NHE9

KC Kondapalli, A Hack, M Schushan, M Landau… - Nature …, 2013 - nature.com
Abstract NHE9 (SLC9A9) is an endosomal cation/proton antiporter with orthologues in yeast
and bacteria. Rare, missense substitutions in NHE9 are genetically linked with autism but …

Organellar Na+/H+ Exchangers: Novel Players in Organelle pH Regulation and Their Emerging Functions

R Ohgaki, SCD van IJzendoorn, M Matsushita… - Biochemistry, 2011 - ACS Publications
Mammalian Na+/H+ exchangers (NHEs) play a fundamental role in cellular ion
homeostasis. NHEs exhibit an appreciable variation in expression, regulation, and …

Emerging roles of Na+/H+ exchangers in epilepsy and developmental brain disorders

H Zhao, KE Carney, L Falgoust, JW Pan, D Sun… - Progress in …, 2016 - Elsevier
Epilepsy is a common central nervous system (CNS) disease characterized by recurrent
transient neurological events occurring due to abnormally excessive or synchronous …

Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

JE Huffman, A Knežević, V Vitart, J Kattla… - Human molecular …, 2011 - academic.oup.com
The majority of human proteins are post-translationally modified by covalent addition of one
or more complex oligosaccharides (glycans). Alterations in glycosylation processing are …