Ion channels in cancer: are cancer hallmarks oncochannelopathies?

N Prevarskaya, R Skryma, Y Shuba - Physiological reviews, 2018 - journals.physiology.org
Genomic instability is a primary cause and fundamental feature of human cancer. However,
all cancer cell genotypes generally translate into several common pathophysiological …

Squeezing for life–properties of red blood cell deformability

R Huisjes, A Bogdanova, WW Van Solinge… - Frontiers in …, 2018 - frontiersin.org
Deformability is an essential feature of blood cells (RBCs) that enables them to travel
through even the smallest capillaries of the human body. Deformability is a function of (i) …

Piezo1 links mechanical forces to red blood cell volume

SM Cahalan, V Lukacs, SS Ranade, S Chien… - elife, 2015 - elifesciences.org
Red blood cells (RBCs) experience significant mechanical forces while recirculating, but the
consequences of these forces are not fully understood. Recent work has shown that gain-of …

Recent advances in the treatment of sickle cell disease

G Salinas Cisneros, SL Thein - Frontiers in physiology, 2020 - frontiersin.org
Sickle cell anemia (SCA) was first described in the Western literature more than 100 years
ago. Elucidation of its molecular basis prompted numerous biochemical and genetic studies …

Treating sickle cell disease by targeting HbS polymerization

WA Eaton, HF Bunn - Blood, The Journal of the American …, 2017 - ashpublications.org
Although the root cause of sickle cell disease is the polymerization of hemoglobin S (HbS) to
form fibers that make red cells less flexible, most drugs currently being assessed in clinical …

[HTML][HTML] Autosomal dominant polycystic kidney disease: the last 3 years

VE Torres, PC Harris - Kidney international, 2009 - Elsevier
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal
monogenic disorder. It has large inter-and intra-familial variability explained to a large extent …

Ion channels as therapeutic targets: a drug discovery perspective

SK Bagal, AD Brown, PJ Cox, K Omoto… - Journal of medicinal …, 2013 - ACS Publications
Ion channels are membrane proteins expressed in almost all living cells. The sequencing of
the human genome has identified more than 400 putative ion channels, but only a fraction of …

[HTML][HTML] Vasculopathy in sickle cell disease: biology, pathophysiology, genetics, translational medicine and new research directions

GJ Kato, RP Hebbel, MH Steinberg… - American journal of …, 2009 - ncbi.nlm.nih.gov
Sickle cell disease has been very well characterized as a single amino acid molecular
disorder of hemoglobin leading to its pathological polymerization, with resulting red cell …

Sickle cell anemia and its phenotypes

TN Williams, SL Thein - Annual review of genomics and human …, 2018 - annualreviews.org
In the 100 years since sickle cell anemia (SCA) was first described in the medical literature,
studies of its molecular and pathophysiological basis have been at the vanguard of scientific …

Sickle cell anemia, the first molecular disease: overview of molecular etiology, pathophysiology, and therapeutic approaches

MH Steinberg - The Scientific World Journal, 2008 - Wiley Online Library
The root cause of sickle cell disease is a single β‐globin gene mutation coding for the sickle
β‐hemoglobin chain. Sickle hemoglobin tetramers polymerize when deoxygenated …