Publications by authors named "N V Bobrova"

Introduction: Idiopathic congenital acorea is extremely rare. There are several techniques for preserving the clear lens during pupil formation.

Case Presentation: The complete pupil absence caused acute glaucoma attack 2 weeks after birth, which was controlled in a 1-month-old child by peripheral iridectomy and disconnecting iris-corneal synechias.

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This feature article is devoted to the evaluation of different techniques for producing colloidal polyelectrolyte brushes (CPEBs) based on cellulose nanofibers modified with grafted polyacrylates. The paper also reviews the potential applications of these CPEBs in designing electrode materials and as reinforcing additives. Additionally, we discuss our own perspectives on investigating composites with CPEBs.

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Objective: Aim: Analysis of trends in the microbial communities of the genitourinary system in patients with urolithiasis.

Patients And Methods: Materials and Methods: 165 urine samples from patients with urolithiasis was examined. The quantitative isolation of microflora was carried out using the bacteriological method.

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Inks for 3D printing were prepared by dispersing bacterial cellulose nanofibers (CNF) functionalized with methacrylate groups in a polymerizable deep eutectic solvent (DES) based on choline chloride and acrylic acid with water as a cosolvent. After 3D printing and UV-curing, the double-network composite gel consisting of chemically and physically crosslinked structures composed from sub-networks of modified CNF and polymerized DES, respectively, was formed. The rheological properties of inks, as well as mechanical and shape memory properties of the 3D-printed gels, were investigated in dynamic and static modes.

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Article Synopsis
  • A study identified pathogenic variants linked to autosomal dominant congenital cataracts in five Ukrainian families, indicating a genetic basis for the condition.
  • Whole-exome sequencing revealed novel mutations in genes such as HSF4, CRYGA, CRYGC, and PAX6, with one known mutation in GJA3.
  • The research highlights the importance of transcription factors and lens crystallins in lens development and the genetic factors influencing cataracts.
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