Results 111 to 120 of about 1,208,260 (137)

Müller cell markers in aqueous humor of patients with type-2 macular telangiectasia. [PDF]

Indian J Ophthalmol
Osmanlı E, Sül S, Kaderli A, Kaderli ST, Türkçü Ü.   +4 more
europepmc   +1 more source

Dysregulation of neurovascular unit in the retina after optic nerve injury. [PDF]

BMC Ophthalmol
Wu Q, Wang H, Liu H, Zhang L, Wei Q.
europepmc   +1 more source

Schwann Cell Expression Pattern in Human Melanomas: In Silico and Immunohistochemical Analyses. [PDF]

Int J Mol Sci
Giampietri C, Somma F, Pizzichini E, D'Arcangelo D, Rahimi S, Fabrizi C, Facchiano A.   +6 more
europepmc   +1 more source

Characterization of a novel variant in KCNJ16, encoding K_ir5.1 channel. [PDF]

Physiol Rep
Xu B, Levchenko V, Bohovyk R, Ahrari A, Geurts AM, Sency V, Xin B, Wang H, Staruschenko A.   +8 more
europepmc   +1 more source

EAST (Epilepsy, Ataxia, Sensorineural Hearing Loss, and Renal Tubulopathy) Syndrome: A Rare Association Between Brain, Ear, and Kidney. [PDF]

Cureus
Vats A, Satpathy A, Sahoo B, Sahoo A, Nayak MK.   +4 more
europepmc   +1 more source

Nonlinear dynamics of seizure suppression via optogenetic modulation of neuron-astrocyte interaction. [PDF]

Sci Rep
Maboodi M, Arabameri A, Bahrami F.
europepmc   +1 more source

The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel

Pflugers Archiv European Journal of Physiology, 2011
Mutations in the K+ channel gene KCNJ10 (Kir4.1) cause the autosomal recessive EAST syndrome which is characterized by epilepsy, ataxia, sensorineural deafness, and a salt-wasting tubulopathy. The renal saltwasting pathology of EAST syndrome is caused by
Detlef Bockenhauer, Richard Warth, Sascha Bandulik   +2 more
exaly   +2 more sources

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

Proceedings of the National Academy of Sciences of the United States of America, 2010
Mutations of the KCNJ10 ( Kir4.1 ) K + channel underlie autosomal recessive epilepsy, ataxia, sensorineural deafness, and (a salt-wasting) renal tubulopathy (EAST ...
Detlef Bockenhauer, Richard Warth, Robert Kleta   +2 more
exaly   +2 more sources

Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling

American Journal of Physiology - Cell Physiology, 2014
We used primary mouse corneal epithelial cells (pMCE) to examine the role of Kcnj10 in determining membrane K(+) conductance and cell membrane potential and in regulating EGF/TGFA release.
Dao-Hong Lin, Chengbiao Zhang
exaly   +2 more sources