Cargando…

Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus

BACKGROUND: The genetic background of type 2 diabetes is complex involving contribution by both nuclear and mitochondrial genes. There is an excess of maternal inheritance in patients with type 2 diabetes and, furthermore, diabetes is a common symptom in patients with mutations in mitochondrial DNA...

Descripción completa

Detalles Bibliográficos
Autores principales:	Soini, Heidi K, Moilanen, Jukka S, Finnila, Saara, Majamaa, Kari
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Short Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434112/ https://www.ncbi.nlm.nih.gov/pubmed/22780954 http://dx.doi.org/10.1186/1756-0500-5-350

Ejemplares similares

Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus
por: Soini, Heidi K, et al.
Publicado: (2013)

Analysis of functional variants in mitochondrial DNA of Finnish athletes
por: Kiiskilä, Jukka, et al.
Publicado: (2019)

A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease
por: Soini, Heidi K., et al.
Publicado: (2017)

Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscripts
por: Kiiskilä, Jukka, et al.
Publicado: (2021)

Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment
por: Häkli, Sanna, et al.
Publicado: (2015)

Whole-loop mitochondrial DNA D-loop sequence variability in Egyptian Arabian equine matrilines
por: Hudson, William
Publicado: (2017)

HTT haplogroups in Finnish patients with Huntington disease
por: Ylönen, Susanna, et al.
Publicado: (2019)

POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
por: Komulainen, Tuomas, et al.
Publicado: (2010)

Comorbid epilepsy in Finnish patients with adult-onset Huntington’s disease
por: Sipilä, Jussi O. T., et al.
Publicado: (2016)

Mitochondrial hearing loss mutations among Finnish preterm and term-born infants
por: Soini, Heidi K., et al.
Publicado: (2017)

Mitochondrial DNA variation in sudden cardiac death: a population-based study
por: Kytövuori, Laura, et al.
Publicado: (2019)

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G
por: Majamaa-Voltti, Kirsi, et al.
Publicado: (2002)

Whole mitochondrial genomes unveil the impact of domestication on goat matrilineal variability
por: Colli, Licia, et al.
Publicado: (2015)

A 13-year follow-up of Finnish patients with Salla disease
por: Paavola, Liisa E., et al.
Publicado: (2015)

Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis
por: Siitonen, Ari, et al.
Publicado: (2019)

Additions to the list of Finnish Bibionomorpha (Diptera, Nematocera)
por: Salmela, Jukka, et al.
Publicado: (2015)

Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degeneration
por: Krüger, Johanna, et al.
Publicado: (2010)

Psychiatric and neurological disorders are associated with bullous pemphigoid – a nationwide Finnish Care Register study
por: Försti, Anna-Kaisa, et al.
Publicado: (2016)

Whole mitochondrial genome analysis in highland Tibetans: further matrilineal genetic structure exploration
por: Li, Xin, et al.
Publicado: (2023)

Working people with type 1 diabetes in the Finnish population
por: Hakkarainen, Pirjo, et al.
Publicado: (2017)

Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts
por: Laaksonen, Jaakko, et al.
Publicado: (2021)

Cost–utility of different treatment strategies after the failure of tumour necrosis factor inhibitor in rheumatoid arthritis in the Finnish setting
por: Hallinen, Taru A., et al.
Publicado: (2010)

Matrilin-3 Role in Cartilage Development and Osteoarthritis
por: Muttigi, Manjunatha S., et al.
Publicado: (2016)

Characterization of recombinantly expressed matrilin VWA domains
por: Becker, Ann-Kathrin A., et al.
Publicado: (2015)

Archaeogenomic evidence reveals prehistoric matrilineal dynasty
por: Kennett, Douglas J., et al.
Publicado: (2017)

Amount of external CME in groups of specialties: a nation-wide survey among Finnish doctors
por: Helin-Salmivaara, Arja, et al.
Publicado: (2009)

Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer families
por: Haanpää, Maria, et al.
Publicado: (2013)

The congruence between matrilineal genetic (mtDNA) and geographic diversity of Iranians and the territorial populations
por: Bahmanimehr, Ardeshir, et al.
Publicado: (2015)

A Matrilineal Study on the Origin and Genetic Relations of the Ecuadorian Pillareño Creole Pig Population through D-Loop Mitochondrial DNA Analysis
por: Vergara, Amado Manuel Canales, et al.
Publicado: (2021)

Evaluation of the Finnish CERN activities: panel report
por: Paul, Peter, et al.
Publicado: (2001)

Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora
por: Behar, Doron M., et al.
Publicado: (2008)

Fibrillin-2, tenascin-C, matrilin-2, and matrilin-4 are strongly expressed in the epithelium of human granular and lattice type I corneal dystrophies
por: Szalai, Eszter, et al.
Publicado: (2012)

Ancient DNA Reveals Matrilineal Continuity in Present-Day Poland over the Last Two Millennia
por: Juras, Anna, et al.
Publicado: (2014)

Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise
por: Kiiskilä, Jukka M., et al.
Publicado: (2022)

Mitochondrial DNA sequence variation and neurodegeneration
por: Mancuso, Michelangelo, et al.
Publicado: (2008)

Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors
por: Crowgey, Erin L, et al.
Publicado: (2020)

Work-related diabetes distress among Finnish workers with type 1 diabetes: a national cross-sectional survey
por: Hakkarainen, Pirjo, et al.
Publicado: (2016)

Analysis of the genetic variation in mitochondrial DNA, Y-chromosome sequences, and MC1R sheds light on the ancestry of Nigerian indigenous pigs
por: Adeola, Adeniyi C., et al.
Publicado: (2017)

A homogenous nature of native Chinese duck matrilineal pool
por: He, Da-Qian, et al.
Publicado: (2008)

Matrilin-2 Is Proteolytically Cleaved by ADAMTS-4 and ADAMTS-5
por: Wang, Zhengke, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_rku0t7njrr8k90u2015ne11tjf