Results 101 to 110 of about 24,513 (256)

MiR-199a-3p/5p participated in TGF-β and EGF induced EMT by targeting DUSP5/MAP3K11 in pterygium

open access: yesJournal of Translational Medicine, 2020
Recently, it has been reported that miRNA is involved in pterygium, however the exact underlying mechanism in pterygium is unrevealed and require further investigation.
Siying He   +9 more
semanticscholar   +1 more source

Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes

open access: yesClinical Genetics, Volume 109, Issue 3, Page 424-436, March 2026.
In 132 individuals with limb anomalies, diagnostic yield was 36% (47/132), including 25 novel variants, three cases with new phenotypes, and two candidate loci, HOXA11 and a small 2q31.1 deletion. Mouse data and exome‐wide analysis, key in identifying the candidate loci, represent an important opportunity for gene discovery.
Akram Mokhtari   +7 more
wiley   +1 more source

The Effects of Job on the Development of Pterygium

open access: yesTürk Oftalmoloji Dergisi, 2013
Purpose: To investigate the effects of job on the development of pterygium. Material and Method: We retrospectively evaluated the files of 182 patients who were diagnosed as having pterygium between August 2012 and October 2012 in the Ophthalmology ...
Emre Gümüş, İbrahim Yaşar
doaj   +1 more source

Cirrhosis of Liver in Patients With Dyskeratosis Congenita: A Report of Two Cases

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
Classical mucocuaneous triad of dyskeratosis congenita in a patient with decompensated cirrhosis. ABSTRACT Dyskeratosis congenita (DC) is a genetic disorder characterized by multisystem involvement. The most commonly affected systems are the mucocutaneous, bone marrow, and lungs.
Bigyan Maharjan   +8 more
wiley   +1 more source

PTERYGIUM

open access: yesThe Professional Medical Journal, 2018
Objective: To study the results of primary pterygium excision through bare scleratechnique with and without intraoperative Mitomycin C use. Study design: This was anexperimental study with randomised controlled trial. Setting and Duration: This study wasconducted at Eye A unit, Khyber Teaching Hospital, Peshawar from May,2007 to April,2009.Methodology:
Muhammad Rafiq   +5 more
openaire   +3 more sources

Effect of pterygium excision on pterygium induced astigmatism.

open access: yesIndian Journal of Ophthalmology, 2003
Pterygium is known to affect refractive astigmatism, which can have a significant impact on vision. This study was undertaken to evaluate the effect of pterygium excision on refractive astigmatism.
Maheshwari Sejal
doaj  

Expression of CD44, PCNA and E-cadherin in pterygium tissues

open access: yesIndian Journal of Ophthalmology
Purpose: Pterygium is a common ocular surface disease defined by fibrovascular conjunctival growth extending onto the cornea. However, its pathogenesis remains unclear.
Humeyra Yıldırım   +2 more
doaj   +1 more source

Comparative analysis of histopathological and clinical characteristics of pterygium [PDF]

open access: yes, 2010
Background/Aim. Pterygium internum presents a significant epidemiological problem. Its etiopathogenesis is still unclear. After surgical removal it shows great tendency to recidives.
Džunić Boban N.   +5 more
core   +1 more source

The in vitro anti-fibrotic effect of Pirfenidone on human pterygium fibroblasts is associated with down-regulation of autocrine TGF-β and MMP-1

open access: yesInternational Journal of Medical Sciences, 2020
We aimed to investigate the in vitro effect of pirfenidone (PFD) on proliferation, migration and collagen contraction of human pterygium fibroblasts (HPFs). HPFs were obtained from tissue explants during pterygium surgery.
Yijin Tao   +8 more
semanticscholar   +1 more source

Identification of a De Novo MAGEL2 Pathogenic Variant in Schaaf–Yang Syndrome and the Importance of Paternal Allele Confirmation

open access: yesJournal of Clinical Laboratory Analysis, Volume 40, Issue 3, February 2026.
This study reports a de novo MAGEL2 pathogenic variant in a patient with Schaaf–Yang syndrome, confirmed through methylation‐sensitive analysis. Combining genomic sequencing with methylation assays helps accurately determine the parental origin of MAGEL2 mutations.
Youn‐Ji Hong   +7 more
wiley   +1 more source

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