Results 61 to 70 of about 406 (136)

MK-n Synthesis Activity of Human UBIAD1 Mutants of Conserved Aminoacids.

open access: yes, 2015
(A) Schematic representation the prenylation mechanisms of MD (MD-d8) conversion to menaquinones (MK-n-d7). (B) MK-n synthetic activity of human UbiA prenyltransferase domain-containing protein 1 (UBIAD1) deletion mutants.
Naoko Okuda (724165)   +10 more
core   +1 more source

Functional characterization of the UBIAD1 protein: The nodal point for vitamin K and cholesterol synthesis. From corneal dystrophies to lifestyle diseases

open access: yes, 2018
UbiA prenyltransferase domain-containing protein 1 (UBIAD1) is a transmembrane enzyme that plays an essential physiological role in the human body. The most important functions of the UBIAD1 protein include (i) the synthesis of endogenous vitamin K, (ii)
Anna Sarosiak, Monika Ołdak
core   +1 more source

Identification of the candidate regions for the family with Schnyder crystalline corneal dystrophy using HH approach.

open access: yes, 2013
(a) RCHHs shared by 10 patients. The RCHH intervals are shown in black. Other autosomal regions are shown in grey as background. (b) RCHHs shared by 1351 and 1425. (c) RCHHs shared by 1351, 1425, and 1438. (d) RCHH shared by 1351, 1425, 1438, and 1349.
Duane L. Guernsey (242977)   +6 more
core   +1 more source

Cogan syndrome: a case report and review of the literature. [PDF]

open access: yesDigit J Ophthalmol, 2023
Kahuam-López N   +5 more
europepmc   +1 more source

Anterior Segment Optical Coherence Tomography in the Diagnosis of Corneal Stromal Dystrophies in Romania. [PDF]

open access: yesMaedica (Bucur)
Gheorghe AG   +4 more
europepmc   +1 more source

Reduced quality of life in corneal dystrophy - a prospective case control study. [PDF]

open access: yesBMC Ophthalmol
Elhardt C   +5 more
europepmc   +1 more source

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