These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 28599824)

  • 81. A single-nucleotide polymorphism in the MicroRNA-146a gene is associated with diabetic nephropathy and sight-threatening diabetic retinopathy in Caucasian patients.
    Kaidonis G; Gillies MC; Abhary S; Liu E; Essex RW; Chang JH; Pal B; Sivaprasad S; Pefkianaki M; Daniell M; Lake S; Petrovsky N; Hewitt AW; Jenkins A; Lamoureux EL; Gleadle JM; Craig JE; Burdon KP
    Acta Diabetol; 2016 Aug; 53(4):643-50. PubMed ID: 26997512
    [TBL] [Abstract][Full Text] [Related]  

  • 82. D-glucose metabolism in lymphocytes of patients with mitochondrial point mutation of the tRNALeu(UUR) gene.
    Malaisse WJ; Pueyo ME; Nadi AB; Malaisse-Lagae F; Froguel P; Velho G
    Biochem Mol Med; 1995 Apr; 54(2):91-5. PubMed ID: 8581364
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects.
    Fukuda M; Nakano S; Imaizumi N; Kitazawa M; Nishizawa M; Kigoshi T; Uchida K
    J Diabetes Complications; 1999; 13(5-6):277-83. PubMed ID: 10765002
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Kishimoto M; Hashiramoto M; Araki S; Ishida Y; Kazumi T; Kanda E; Kasuga M
    Diabetologia; 1995 Feb; 38(2):193-200. PubMed ID: 7713314
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Maternal-foetal complications in pregnancy: a retrospective comparison between type 1 and type 2 diabetes mellitus.
    Guarnotta V; Mineo MI; Giacchetto E; Imbergamo MP; Giordano C
    BMC Pregnancy Childbirth; 2021 Mar; 21(1):243. PubMed ID: 33752628
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study.
    Martikainen MH; Rönnemaa T; Majamaa K
    Acta Diabetol; 2013 Oct; 50(5):737-41. PubMed ID: 22492248
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Mitochondrial diabetes mellitus: a review.
    Gerbitz KD; van den Ouweland JM; Maassen JA; Jaksch M
    Biochim Biophys Acta; 1995 May; 1271(1):253-60. PubMed ID: 7599217
    [TBL] [Abstract][Full Text] [Related]  

  • 88. A family with diabetes and heart failure.
    Gerber B; Manser C; Wiesli P; Meier CA
    BMJ Case Rep; 2010 Oct; 2010():. PubMed ID: 22790282
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Correlation of Osteoporosis in Patients With Newly Diagnosed Type 2 Diabetes: A Retrospective Study in Chinese Population.
    Wen Y; Li H; Zhang X; Liu P; Ma J; Zhang L; Zhang K; Song L
    Front Endocrinol (Lausanne); 2021; 12():531904. PubMed ID: 34054717
    [TBL] [Abstract][Full Text] [Related]  

  • 90. A review of maternally inherited diabetes and deafness.
    Li HZ; Li RY; Li M
    Front Biosci (Landmark Ed); 2014 Jan; 19(5):777-82. PubMed ID: 24389221
    [TBL] [Abstract][Full Text] [Related]  

  • 91. [Maternally Inherited Diabetes and Deafness].
    Sampedro A; Barbón JJ; Alvarez JA; Andrés MA; Baldó C
    Arch Soc Esp Oftalmol; 2009 Jul; 84(7):359-61. PubMed ID: 19658054
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Type 1 diabetes and celiac disease in adults: glycemic control and diabetic complications.
    Bakker SF; Tushuizen ME; von Blomberg ME; Mulder CJ; Simsek S
    Acta Diabetol; 2013 Jun; 50(3):319-24. PubMed ID: 22539236
    [TBL] [Abstract][Full Text] [Related]  

  • 93. The mitochondrial tRNA[Leu(UUR)] A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population.
    Smith PR; Dronsfield MJ; Mijovic CH; Hattersley AT; Yeung VT; Cockram C; Chan JC; Barnett AH; Bain SC
    Diabet Med; 1997 Dec; 14(12):1026-31. PubMed ID: 9455929
    [TBL] [Abstract][Full Text] [Related]  

  • 94. [Mitochondrial diabetes: clinical features, diagnosis and management].
    Meas T; Laloi-Michelin M; Virally M; Ambonville C; Kevorkian JP; Guillausseau PJ
    Rev Med Interne; 2010 Mar; 31(3):216-21. PubMed ID: 19299044
    [TBL] [Abstract][Full Text] [Related]  

  • 95. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.
    Tabebi M; Mkaouar-Rebai E; Mnif M; Kallabi F; Ben Mahmoud A; Ben Saad W; Charfi N; Keskes-Ammar L; Kamoun H; Abid M; Fakhfakh F
    Biochem Biophys Res Commun; 2015 Apr; 459(3):353-60. PubMed ID: 25701779
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Prevalence of maternally inherited diabetes and deafness in Australian diabetic subjects.
    Holmes-Walker DJ; Boyages SC
    Diabetologia; 1999 Aug; 42(8):1028-9. PubMed ID: 10491766
    [No Abstract]   [Full Text] [Related]  

  • 97. Serum adiponectin helps to differentiate type 1 and type 2 diabetes among young Asian Indians.
    Gokulakrishnan K; Aravindhan V; Amutha A; Abhijit S; Ranjani H; Anjana RM; Unnikrishnan R; Miranda P; Narayan KM; Mohan V
    Diabetes Technol Ther; 2013 Aug; 15(8):696-702. PubMed ID: 23902401
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Clustering of long-term complications in families with diabetes in the diabetes control and complications trial. The Diabetes Control and Complications Trial Research Group.
    Diabetes; 1997 Nov; 46(11):1829-39. PubMed ID: 9356033
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Ptosis as an associated finding in maternally inherited diabetes and deafness.
    Robberecht K; Decock C; Stevens A; Seneca S; De Bleecker J; Leroy BP
    Ophthalmic Genet; 2010 Dec; 31(4):240-3. PubMed ID: 21067488
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Brain anomalies in maternally inherited diabetes and deafness syndrome.
    Fromont I; Nicoli F; Valéro R; Felician O; Lebail B; Lefur Y; Mancini J; Paquis-Flucklinger V; Cozzone PJ; Vialettes B
    J Neurol; 2009 Oct; 256(10):1696-704. PubMed ID: 19536585
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.