Cargando…

Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathy

PURPOSE: The association of non-synonymous substitution polymorphism rs1801282 (c.34C>G, p.Pro12Ala) in exon 4 of the peroxisome proliferator activated receptor gamma gene with diabetic retinopathy (DR) has been reported inconsistently. Therefore, the purpose of the present study was to understan...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tariq, Khadija, Malik, Saira Bano, Ali, Syeda Hafiza Benish, Maqsood, Sundas Ejaz, Azam, Aisha, Muslim, Irfan, Khan, Muhammad Shakil, Azam, Maleeha, Waheed, Nadia Khalida, Qamar, Raheel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Molecular Vision 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611930/ https://www.ncbi.nlm.nih.gov/pubmed/23559865

Ejemplares similares

Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy
por: Saleem, Saba, et al.
Publicado: (2015)

Exome Sequencing Identifies Three Novel Candidate Genes Implicated in Intellectual Disability
por: Agha, Zehra, et al.
Publicado: (2014)

Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan
por: Maria, Maleeha, et al.
Publicado: (2015)

Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families
por: Ajmal, Muhammad, et al.
Publicado: (2012)

XRCC1 and XPD DNA repair gene polymorphisms: A potential risk factor for glaucoma in the Pakistani population
por: Yousaf, Sajeela, et al.
Publicado: (2011)

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease
por: Waheed, Nadia K., et al.
Publicado: (2012)

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome
por: Ajmal, Muhammad, et al.
Publicado: (2013)

Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous Family
por: Ghafoor, Saima, et al.
Publicado: (2022)

Association of IL-17A promoter region SNP-rs2275913 with urinary bladder cancer
por: Anwar, Maryam, et al.
Publicado: (2023)

Association of IGF1 polymorphisms with exotropia in a Pakistani cohort
por: Zehra, Zainab, et al.
Publicado: (2022)

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts
por: Ayub, Humaira, et al.
Publicado: (2010)

Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa
por: Ajmal, Muhammad, et al.
Publicado: (2012)

The Molecular Basis of Retinal Dystrophies in Pakistan
por: Khan, Muhammad Imran, et al.
Publicado: (2014)

Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7
por: Van Schil, Kristof, et al.
Publicado: (2016)

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
por: Azam, Maleeha, et al.
Publicado: (2009)

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa
por: Azam, Maleeha, et al.
Publicado: (2009)

Genotyping of peroxisome proliferator-activated receptor gamma (PPAR-γ) polymorphism (Pro12Ala) in Iranian population
por: Namvaran, Fatemeh, et al.
Publicado: (2011)

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa
por: Khan, Muhammad Imran, et al.
Publicado: (2010)

Boc-AzAla-Ala-OMe
por: Abbas, Cécile, et al.
Publicado: (2009)

Association between the Pro12Ala Polymorphism of the Peroxisome Proliferator-Activated Receptor Gamma Gene and Strength Athlete Status
por: Maciejewska-Karlowska, Agnieszka, et al.
Publicado: (2013)

Cardiomyopathy associated with the Ala143Thr variant of the α-galactosidase A gene
por: Valtola, Kati, et al.
Publicado: (2020)

Synthesis, DFT and molecular docking of novel (Z)-4-bromo-N-(4-butyl-3 (quinolin-3-yl)thiazol-2(3H)-ylidene)benzamide as elastase inhibitor
por: Mustafa, Muhammad Naeem, et al.
Publicado: (2023)

PMON130 Pituitary apoplexy presenting as left basal ganglia hemorrhage
por: Zahid, Maleeha, et al.
Publicado: (2022)

THU369 A Rare Case Of IgG4-related Autoimmune Pancreatitis And Diabetes Mellitus
por: Zahid, Maleeha, et al.
Publicado: (2023)

Late-onset and classic phenotypes of Fabry disease in males with the GLA-Thr410Ala mutation
por: Valtola, Kati, et al.
Publicado: (2023)

Gain of C-Ala enables AlaRS to target the L-shaped tRNA(Ala)
por: Antika, Titi Rindi, et al.
Publicado: (2022)

Assessment during Covid-19: quality assurance of an online open book formative examination for undergraduate medical students
por: Rehman, Javeria, et al.
Publicado: (2022)

Evaluation of single nucleotide polymorphisms of Pro12Ala in peroxisome proliferator-activated receptor-γ and Gly308Ala in tumor necrosis factor-α genes in obese Asian Indians: a population-based study
por: Bhagat, Namita, et al.
Publicado: (2010)

Distribution and genotype frequency of the C1431T and pro12ala polymorphisms of the peroxisome proliferator activator receptor gamma gene in an Iranian population
por: Rooki, Hassan, et al.
Publicado: (2013)

Peroxisome proliferator-activated receptor Pro12Ala polymorphism and the risks of gestational diabetes mellitus: An updated meta-analysis of 12 studies
por: Wang, Lihong, et al.
Publicado: (2016)

Pro12Ala polymorphism of peroxisome proliferator activated receptor gamma 2 may be associated with adverse neurodevelopment in European preterm babies
por: Victor, Suresh, et al.
Publicado: (2021)

Smoke produced from plants waste material elicits growth of wheat (Triticum aestivum L.) by improving morphological, physiological and biochemical activity
por: Iqbal, Muhammad, et al.
Publicado: (2017)

Alas rotas /
por: Gibran, Kahlil, 1883-1931
Publicado: (1999)

Alas erratiles
por: Muñoz Avila, Adalberto
Publicado: (1976)

Association between the Pro12Ala Polymorphism of Peroxisome Proliferator-Activated Receptor Gamma 2 and Inflammatory Bowel Disease: A Meta-Analysis
por: Zhang, Zhi-Feng, et al.
Publicado: (2012)

Effect of the Pro12Ala Polymorphism of the Peroxisome Proliferator-activated Receptor γ2 Gene on Lipid Profile and Adipokines Levels in Obese Subjects
por: Becer, E, et al.
Publicado: (2017)

Association between peroxisome proliferator-activated receptor γ-2 gene Pro12Ala polymorphisms and risk of hypertension: an updated meta-analysis
por: Zhang, Miao, et al.
Publicado: (2019)

In Silico Drug Designing for ala438 Deleted Ribosomal Protein S1 (RpsA) on the Basis of the Active Compound Zrl15
por: Wadood, Abdul, et al.
Publicado: (2021)

A Case of Rapidly Proliferative Glomerulonephritis Secondary to Syphilis That Responded to Treatment With Penicillin
por: Siddiqui, Raheel S, et al.
Publicado: (2021)

Comparative Modeling and Analysis of Extremophilic D-Ala-D-Ala Carboxypeptidases
por: Diessner, Elizabeth M., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_prcvr7vjs7rl23rs4ceuc90hst