Results 41 to 50 of about 83,153 (169)
Class I HDAC imaging using [3H]CI-994 autoradiography
[3H]CI-994, a radioactive isotopologue of the benzamide CI-994, a class I histone deacetylase inhibitor (HDACi), was evaluated as an autoradiography probe for ex vivo labeling and localizing of class I HDAC (isoforms 1–3) in the rodent brain.
Hong, Yijia +10 more
core +1 more source
CLITEMNESTRA Y LA RETÓRICA DEL ENGAÑO (AG.907-994) [PDF]
CLITEMNESTRA Y LA RETÓRICA DEL ENGAÑO (AG.907 ...
Gastaldi, Viviana
core +1 more source
To report a rare case of extrusion of Aurolab aqueous drainage implant (AADI). A 65-year-old male presented with a history of blunt trauma, loss of vision, and irritation in his left eye (oculus sinister [OS]) for 1 year.
Devendra Maheshwari +4 more
doaj +1 more source
Congenital stationary night blindness linked to a CACNA1F gene mutation [PDF]
Congenital stationary night blindness encompasses a heterogeneous group of inherited retinal dystrophies characterized by impaired scotopic vision from birth.
Flávio Mac Cord Medina +4 more
doaj +1 more source
Is RE1/NRSE a Common cis -Regulatory Sequence for ChAT and VAChT Genes?
International audienceCholine acetyltransferase (ChAT), the biosynthetic enzyme of acetylcholine, and the vesicular acetylcholine transporter (VAChT) are both required for cholinergic neurotransmission.
Vodjdani, Guilan +8 more
core +1 more source
Purpose. To present the development stages and results of 18 years of experience in laser technologies application for the treatment of premature infants with active ROP in the Kaluga branch of S.
A.V. Tereshchenko +4 more
doaj +1 more source
Complex Ba(RE1/2Ta1/2)O3 [RE = rare earth] ceramics have been prepared by solid state ceramic route and their microwave dielectric responses were measured in the GHz range. In general, the resonators showed high dielectric constants, high quality factors
Moreira, Roberto Luiz +3 more
core +2 more sources
Typical presentation of autosomal recessive oculocutaneous albinism in two siblings
Objective: We report the case history and clinical findings in two siblings, a 13-year-old male and a 10-year-old female, who presented with complaints of poor vision since childhood. Both children had blonde hair and depigmented skin.
Nishant, Prateek +3 more
doaj +1 more source

