186 related articles for article (PubMed ID: 33728047)
1. Next-generation sequencing of the whole mitochondrial genome identifies novel and common variants in patients with psoriasis, type 2 diabetes mellitus and psoriasis with comorbid type 2 diabetes mellitus.
Alwehaidah MS; Al-Kafaji G; Bakhiet M; Alfadhli S
Biomed Rep; 2021 May; 14(5):41. PubMed ID: 33728047
[TBL] [Abstract][Full Text] [Related]
2. Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
Al-Kafaji G; Bakheit HF; AlAli F; Fattah M; Alhajeri S; Alharbi MA; Daif A; Alsabbagh MM; Alwehaidah MS; Bakhiet M
PLoS One; 2022; 17(2):e0263606. PubMed ID: 35130313
[TBL] [Abstract][Full Text] [Related]
3. Genomic profiling of mitochondrial DNA reveals novel complex gene mutations in familial type 2 diabetes mellitus individuals from Mizo ethnic population, Northeast India.
Lalrohlui F; Zohmingthanga J; Hruaii V; Kumar NS
Mitochondrion; 2020 Mar; 51():7-14. PubMed ID: 31862415
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial Haplogroup Reveals the Genetic Basis of Diabetes Mellitus Type 2 Comorbidity in Psoriasis.
Alwehaidah MS; Bakhiet M; AlFadhli S
Med Princ Pract; 2021; 30(1):62-68. PubMed ID: 32629455
[TBL] [Abstract][Full Text] [Related]
5. De-regulation of diabetic regulatory genes in psoriasis: Deciphering the unsolved riddle.
AlFadhli S; Al-Zufairi AAM; Nizam R; AlSaffar HA; Al-Mutairi N
Gene; 2016 Nov; 593(1):110-116. PubMed ID: 27530212
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of D-loop hypervariable region I variations, haplogroups and copy number of mitochondrial DNA in Bangladeshi population with type 2 diabetes.
Saha SK; Saba AA; Hasib M; Rimon RA; Hasan I; Alam MS; Mahmud I; Nabi AHMN
Heliyon; 2021 Jul; 7(7):e07573. PubMed ID: 34377852
[TBL] [Abstract][Full Text] [Related]
7. Next-generation re-sequencing of genes involved in increased platelet reactivity in diabetic patients on acetylsalicylic acid.
Postula M; Janicki PK; Eyileten C; Rosiak M; Kaplon-Cieslicka A; Sugino S; Wilimski R; Kosior DA; Opolski G; Filipiak KJ; Mirowska-Guzel D
Platelets; 2016 Jun; 27(4):357-64. PubMed ID: 26599574
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial mutations in subjects with psychiatric disorders.
Sequeira A; Rollins B; Magnan C; van Oven M; Baldi P; Myers RM; Barchas JD; Schatzberg AF; Watson SJ; Akil H; Bunney WE; Vawter MP
PLoS One; 2015; 10(5):e0127280. PubMed ID: 26011537
[TBL] [Abstract][Full Text] [Related]
9. Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals.
Bansal V; Gassenhuber J; Phillips T; Oliveira G; Harbaugh R; Villarasa N; Topol EJ; Seufferlein T; Boehm BO
BMC Med; 2017 Dec; 15(1):213. PubMed ID: 29207974
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide mitochondrial DNA sequence variations and lower expression of OXPHOS genes predict mitochondrial dysfunction in oral cancer tissue.
Chattopadhyay E; De Sarkar N; Singh R; Ray A; Roy R; Paul RR; Pal M; Ghose S; Ghosh S; Kabiraj D; Banerjee R; Roy B
Tumour Biol; 2016 Sep; 37(9):11861-11871. PubMed ID: 27055661
[TBL] [Abstract][Full Text] [Related]
11. Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variants.
Wani AA; Ahanger SH; Bapat SA; Rangrez AY; Hingankar N; Suresh CG; Barnabas S; Patole MS; Shouche YS
PLoS One; 2007 Sep; 2(9):e942. PubMed ID: 17895983
[TBL] [Abstract][Full Text] [Related]
12. mtDNA Single-Nucleotide Variants Associated with Type 2 Diabetes.
Garcia-Gaona E; García-Gregorio A; García-Jiménez C; López-Olaiz MA; Mendoza-Ramírez P; Fernandez-Guzman D; Pillado-Sánchez RA; Soto-Pacheco AD; Yareni-Zuñiga L; Sánchez-Parada MG; González-Santiago AE; Román-Pintos LM; Castañeda-Arellano R; Hernández-Ortega LD; Mercado-Sesma AR; Orozco-Luna FJ; Villa-Angulo C; Villa-Angulo R; Baptista-Rosas RC
Curr Issues Mol Biol; 2023 Oct; 45(11):8716-8732. PubMed ID: 37998725
[TBL] [Abstract][Full Text] [Related]
13. Absence of mtDNA mutations in leukocytes of CADASIL patients.
Abu-Amero KK; Hellani A; Bohlega S
BMC Res Notes; 2008 May; 1():16. PubMed ID: 18710532
[TBL] [Abstract][Full Text] [Related]
14.
Dashti M; Nizam R; John SE; Melhem M; Channanath A; Alkandari H; Thanaraj TA; Al-Mulla F
Front Genet; 2023; 14():1254833. PubMed ID: 37941991
[No Abstract] [Full Text] [Related]
15. Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.
Charoute H; Kefi R; Bounaceur S; Benrahma H; Reguig A; Kandil M; Rouba H; Bakhchane A; Abdelhak S; Barakat A
Mitochondrial DNA A DNA Mapp Seq Anal; 2018 Jan; 29(1):9-13. PubMed ID: 27728995
[TBL] [Abstract][Full Text] [Related]
16. Polymorphisms in the Mitochondrial Genome Are Associated With Bullous Pemphigoid in Germans.
Russlies J; Fähnrich A; Witte M; Yin J; Benoit S; Gläser R; Günter C; Eming R; Erdmann J; Gola D; Gupta Y; Holtsche MM; Kern JS; König IR; Kiritsi D; Lieb W; Sadik CD; Sárdy M; Schauer F; van Beek N; Weidinger A; Worm M; Zillikens D; Schmidt E; Busch H; Ibrahim SM; Hirose M
Front Immunol; 2019; 10():2200. PubMed ID: 31824475
[TBL] [Abstract][Full Text] [Related]
17. Diabetes and branched-chain amino acids: What is the link?
Bloomgarden Z
J Diabetes; 2018 May; 10(5):350-352. PubMed ID: 29369529
[TBL] [Abstract][Full Text] [Related]
18. Four novel mutations in the mitochondrial
Alharbi MA; Al-Kafaji G; Khalaf NB; Messaoudi SA; Taha S; Daif A; Bakhiet M
Biomed Rep; 2019 Dec; 11(6):257-268. PubMed ID: 31798871
[TBL] [Abstract][Full Text] [Related]
19. Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.
Choo-Kang AT; Lynn S; Taylor GA; Daly ME; Sihota SS; Wardell TM; Chinnery PF; Turnbull DM; Walker M
Diabetes; 2002 Jul; 51(7):2317-20. PubMed ID: 12086967
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia.
Torrell H; Salas A; Abasolo N; Morén C; Garrabou G; Valero J; Alonso Y; Vilella E; Costas J; Martorell L
Am J Med Genet B Neuropsychiatr Genet; 2014 Oct; 165B(7):607-17. PubMed ID: 25132006
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
