Purification and properties of pyrimidine dimer specific endonucleases from Micrococcus luteus

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

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INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family.

Clinical genetics·2017

Vitamin E protects rat mesenchymal stem cells against hydrogen peroxide-induced oxidative stress in vitro and improves their therapeutic potential in surgically-induced rat model of osteoarthritis.

Osteoarthritis and cartilage·2016

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Clinical genetics·2016

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Molecular psychiatry·2016

A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred.

Clinical genetics·2015

Clinical Europium fluorescent based lectin assays for mucin O-glycomics.

Methods in enzymology·2026

A dual-color FRET assay for detection and quantitative analysis of O-glycopeptidases.

Methods in enzymology·2026

Evolutionary genetic approaches to analyze mucins.

Methods in enzymology·2026

Ex vivo imaging and enzymatic analysis of intestinal mucus.

Methods in enzymology·2026

Glyco-TRAPP: A real-time glycocalyx permeability assay for assessing transmembrane mucin barrier function in live and fixed tissues.

Methods in enzymology·2026

Quantitative imaging approaches to capture structural and functional dynamics of colonic mucus in health and disease in situ.

Methods in enzymology·2026

Risk factors associated with complications in surgical treatment of mandibular fractures: a retrospective study.

The British journal of oral & maxillofacial surgery·2026

Prognostic Impact of Sequential Measurable Residual Disease and KIT Variant Status in Pediatric Core-Binding Factor Acute Myeloid Leukemia: A Retrospective Multicenter Study of the Taiwan Pediatric Oncology Group.

Annals of laboratory medicine·2026

Primary diffuse leptomeningeal melanomatosis presenting as chronic meningitis and dense spinal plaques.

Practical neurology·2026

Empiric MRSA Coverage for Children with Osteoarticular Infections: 2015 to 2024.

Pediatrics·2026

High-dose inhaled nitric oxide for severe pneumonia caused by multidrug-resistant bacteria: a randomized controlled trial protocol.

Annals of medicine·2026

Antimicrobial and Antiviral Effects of Viscous Mouthwash Containing Cetylpyridinium Chloride and Isopropyl Methylphenol.

Journal of dentistry·2026

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Purification and properties of pyrimidine dimer specific endonucleases from Micrococcus luteus

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Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family.

Vitamin E protects rat mesenchymal stem cells against hydrogen peroxide-induced oxidative stress in vitro and improves their therapeutic potential in surgically-induced rat model of osteoarthritis.

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred.

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Purification and properties of pyrimidine dimer specific endonucleases from Micrococcus luteus

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