Cargando…

Population Specific Impact of Genetic Variants in KCNJ11 Gene to Type 2 Diabetes: A Case-Control and Meta-Analysis Study

BACKGROUND AND OBJECTIVES: Potassium inwardly rectifying channel, subfamily J, member 11 (KCNJ11) gene have a key role in insulin secretion and is of substantial interest as a candidate gene for type 2 diabetes (T2D). The current work was performed to delineate the genetic influence of KCNJ11 polymo...

Descripción completa

Detalles Bibliográficos
Autores principales:	Phani, Nagaraja M., Guddattu, Vasudeva, Bellampalli, Ravishankara, Seenappa, Venu, Adhikari, Prabha, Nagri, Shivashankara K., D′Souza, Sydney C., Mundyat, Gopinath P., Satyamoorthy, Kapaettu, Rai, Padmalatha S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172481/ https://www.ncbi.nlm.nih.gov/pubmed/25247988 http://dx.doi.org/10.1371/journal.pone.0107021

Ejemplares similares

Impact of KCNJ11, TCF7L2, SLC30A8, IGF2BP2, PPARG, SLC47A1, STK11, HHEX, KCNQ1, CDKAL1, FTO, CYP2C9, ADIPOQ, CAPN10 gene polymorphisms on risk of type 2 diabetes and therapeutic response to sulfonylurea and metformin therapy
por: Phani, Nagaraja, et al.
Publicado: (2014)

Replication and Relevance of Multiple Susceptibility Loci Discovered from Genome Wide Association Studies for Type 2 Diabetes in an Indian Population
por: Phani, Nagaraja M., et al.
Publicado: (2016)

Effect of licorice on patients with HSD11B1 gene polymorphisms- a pilot study
por: Devang, Nayana, et al.
Publicado: (2021)

DNA barcoding of authentic and substitute samples of herb of the family Asparagaceae and Asclepiadaceae based on the ITS2 region
por: Rai, Padmalatha S, et al.
Publicado: (2012)

Development of allele specific hybridization assay and computer aided tool for detection of genetic variations in folate pathway genes
por: Ravishankara, et al.
Publicado: (2014)

Pharmacogenomic considerations for repurposing of dexamethasone as a potential drug against SARS-CoV-2 infection
por: Vohra, Manik, et al.
Publicado: (2021)

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type
por: Girisha, Katta Mohan, et al.
Publicado: (2012)

Elevated homocysteine levels in type 2 diabetes induce constitutive neutrophil extracellular traps
por: Joshi, Manjunath B, et al.
Publicado: (2016)

Pharmacogenomics deliberations of 2-deoxy-d-glucose in the treatment of COVID-19 disease: an in silico approach
por: Prabhu, Navya B., et al.
Publicado: (2022)

In vitro bioproduction and enhancement of moscatilin from a threatened tropical epiphytic orchid, Dendrobium ovatum (Willd.) Kraenzl
por: Pujari, Ipsita, et al.
Publicado: (2021)

MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India
por: Cyril, Cyrus, et al.
Publicado: (2009)

Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome
por: Moka, Rajasekhar, et al.
Publicado: (2013)

Brahmarasayana protects against Ethyl methanesulfonate or Methyl methanesulfonate induced chromosomal aberrations in mouse bone marrow cells
por: Guruprasad, Kanive Parashiva, et al.
Publicado: (2012)

Spectrum of bacterial infections and predictors of mortality in adult cirrhotic patients
por: Kudru, Chandrashekar Udyavara, et al.
Publicado: (2019)

Cervical cytology and associated factors among tribal women of Karnataka, India
por: Ghosh, Supriti, et al.
Publicado: (2021)

A novel mutation KCNJ11 R136C caused KCNJ11-MODY
por: Chen, Yaning, et al.
Publicado: (2021)

Cytotoxicity and radiosensitizing potency of Moscatilin in cancer cells at low radiation doses of X-ray and UV-C
por: Pujari, Ipsita, et al.
Publicado: (2021)

Distinct metabolic signatures in blood plasma of bisphenol A–exposed women with polycystic ovarian syndrome
por: Prabhu, Navya B., et al.
Publicado: (2023)

Neonatal Screening for Congenital Adrenal Hyperplasia in Indian Newborns with Reflex Genetic Analysis of 21-Hydroxylase Deficiency
por: Tippabathani, Jayakrishna, et al.
Publicado: (2023)

Comparative analysis of copy number variations in ulcerative colitis associated and sporadic colorectal neoplasia
por: Shivakumar, B. M., et al.
Publicado: (2016)

An Indian Child with CONDSIAS Due to a Novel Variant in ADPRHL2 Gene
por: Bajaj, Shruti, et al.
Publicado: (2022)

KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus
por: Haghvirdizadeh, Polin, et al.
Publicado: (2015)

Psychiatric morbidity in children with KCNJ11 neonatal diabetes
por: Bowman, P., et al.
Publicado: (2016)

Genetic variation in genes involved in folate and drug metabolism in a south Indian population
por: Rai, Padmalatha S, et al.
Publicado: (2011)

Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy
por: Schoeler, Natasha E., et al.
Publicado: (2015)

Genetic and epigenetic changes in host ABCB1 influences malaria susceptibility to Plasmodium falciparum
por: Gupta, Himanshu, et al.
Publicado: (2017)

Mutational analysis of KCNJ11 in Chinese elderly essential hypertensive patients
por: Li, Jia-Yue, et al.
Publicado: (2012)

A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes
por: Gole, Evangelia, et al.
Publicado: (2018)

DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea
por: Cho, Ja Hyang, et al.
Publicado: (2017)

Is methicillin-resistant Staphylococcus Aureus infection associated with higher mortality and morbidity in hospitalized patients? A cohort study of 551 patients from South Western India
por: Chatterjee, Aparajita, et al.
Publicado: (2018)

Immunophenotyping of normal individuals classified on the basis of human dosha prakriti
por: Rotti, Harish, et al.
Publicado: (2014)

Understanding the Change in the Prevalence and Factors Influencing the Childhood Stunting Using District-Level Data from NFHS-4 and NFHS-5 in India
por: B.S., Pooja, et al.
Publicado: (2022)

Public Health Genomics: the essential part for good governance in public health
por: Brand, Angela, et al.
Publicado: (2016)

Oxidative Stress in Cognitive and Epigenetic Aging: A Retrospective Glance
por: Kandlur, Aditi, et al.
Publicado: (2020)

Study on the correlation between KCNJ11 gene polymorphism and metabolic syndrome in the elderly
por: Jiang, Fan, et al.
Publicado: (2017)

SUN-278 Neonatal Diabetes in an Infant with Heterozygous Mutation in KCNJ11 Gene
por: Kota, Archana, et al.
Publicado: (2019)

The E23K Polymorphism of KCNJ11 and Diabetic Retinopathy in Northern Iran
por: Alidoust, L., et al.
Publicado: (2022)

Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants with Congenital Hyperinsulinism
por: Hashemian, Somayyeh, et al.
Publicado: (2021)

Role of IL-6/JAK/STAT pathway in inducing vascular insulin resistance
por: Balakrishnan, Aswath, et al.
Publicado: (2014)

CmirC: an integrated database of clustered miRNAs co-localized with copy number variations in cancer
por: Ware, Akshay Pramod, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_0elm317naqju3dif73qf1kdgq2