Results 31 to 40 of about 2,132 (150)

Identification of transient receptor potential channel genes from the swimming crab, Portunus Trituberculatus, and their expression profiles under acute temperature stress [PDF]

open access: yesBMC Genomics
Background Temperature is an important environment factor that is critical to the survival and growth of crustaceans. However, the mechanisms by which crustaceans detect changes in temperature are still unclear.
Yichen Qian   +5 more
doaj   +2 more sources

Endolysosomal TRPMLs in Cancer [PDF]

open access: yesBiomolecules, 2021
Lysosomes, the degradative endpoints and sophisticated cellular signaling hubs, are emerging as intracellular Ca2+ stores that govern multiple cellular processes. Dys-homeostasis of lysosomal Ca2+ is intimately associated with a variety of human diseases including cancer. Recent studies have suggested that the Ca2+-permeable channels Transient Receptor
Mengnan Xu, Xian-Ping Dong
openaire   +3 more sources

Evolutionary Aspects of TRPMLs and TPCs [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
Transient receptor potential (TRP) or transient receptor potential channels are a highly diverse family of mostly non-selective cation channels. In the mammalian genome, 28 members can be identified, most of them being expressed predominantly in the plasma membrane with the exception of the mucolipins or TRPMLs which are expressed in the endo-lysosomal
Dawid Jaślan   +3 more
openaire   +2 more sources

TRPML Subfamily of Endolysosomal Channels

open access: yes, 2020
Nicholas E. Karagas   +2 more
openaire   +2 more sources

Endolysosomal Cation Channels and Lung Disease

open access: yesCells, 2022
Endolysosomal cation channels are emerging as key players of endolysosomal function such as endolysosomal trafficking, fusion/fission, lysosomal pH regulation, autophagy, lysosomal exocytosis, and endocytosis.
Barbara Spix   +5 more
doaj   +1 more source

Neurodegenerative Lysosomal Storage Disorders: TPC2 Comes to the Rescue!

open access: yesCells, 2022
Lysosomal storage diseases (LSDs) resulting from inherited gene mutations constitute a family of disorders that disturb lysosomal degradative function leading to abnormal storage of macromolecular substrates.
Sandra Prat Castro   +5 more
doaj   +1 more source

Endolysosomal Cation Channels and MITF in Melanocytes and Melanoma

open access: yesBiomolecules, 2021
Microphthalmia-associated transcription factor (MITF) is the principal transcription factor regulating pivotal processes in melanoma cell development, growth, survival, proliferation, differentiation and invasion. In recent years, convincing evidence has
Carla Abrahamian, Christian Grimm
doaj   +1 more source

The role of TRPMLs in endolysosomal trafficking and function [PDF]

open access: yesCell Calcium, 2015
Members of the Transient Receptor Potential-Mucolipin (TRPML) constitute a family of evolutionarily conserved cation channels that function predominantly in endolysosomal vesicles. Whereas loss-of-function mutations in human TRPML1 were first identified as being causative for the lysosomal storage disease, Mucolipidosis type IV, most mammals also ...
Kartik, Venkatachalam   +2 more
openaire   +2 more sources

Ion Channels and Pumps in Autophagy: A Reciprocal Relationship

open access: yesCells, 2021
Autophagy, the process of cellular self-degradation, is intrinsically tied to the degradative function of the lysosome. Several diseases have been linked to lysosomal degradative defects, including rare lysosomal storage disorders and neurodegenerative ...
Hussein Abuammar   +6 more
doaj   +1 more source

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