Page last updated: 2024-10-16

adenine and Deafness

adenine has been researched along with Deafness in 11 studies

Deafness: A general term for the complete loss of the ability to hear from both ears.

Research Excerpts

ExcerptRelevanceReference
"One hundred patients with type 2 diabetes and one hundred healthy control subjects were recruited to participate in the study."1.42Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation. ( Ji, JJ; Li, YX; Li, ZY; Min, R; Tong, AL; Xu, JP; Zhang, HB; Zhang, S; Zhou, MC, 2015)
"Puncture of the cysts followed by administration of antibiotics resulted in marked improvement of symptoms and laboratory findings."1.32Pelvic lymphocyst infection associated with maternally inherited diabetes mellitus. ( Asada, M; Makino, H; Matsuda, M; Ogawa, D; Shikata, K; Uchida, H; Wada, J, 2003)
" This protocol was aimed at assessing two sensitive measures of beta-cell dysfunction: the priming effect of glucose on the glucose-insulin secretion rate (ISR) dose-response curve and the ability of oscillatory glucose infusion to entrain insulin secretory oscillations."1.29Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation. ( Blanché, H; Byrne, MM; Clément, K; Fiet, J; Froguel, P; Passa, P; Polonsky, KS; Pueyo, ME; Robert, JJ; Sturis, J; Velho, G; Vionnet, N, 1996)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (36.36)18.2507
2000's5 (45.45)29.6817
2010's2 (18.18)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Zhou, MC1
Min, R1
Ji, JJ1
Zhang, S1
Tong, AL1
Xu, JP1
Li, ZY1
Zhang, HB1
Li, YX1
Wang, X2
Lu, J2
Zhu, Y2
Yang, A1
Yang, L2
Li, R1
Chen, B1
Qian, Y2
Tang, X2
Wang, J2
Zhang, X2
Guan, MX2
Bai, Y1
Wang, Z1
Dai, W1
Li, Q1
Chen, G1
Cong, N1
Guan, M1
Li, H1
Ogawa, D1
Shikata, K1
Matsuda, M1
Wada, J1
Uchida, H1
Asada, M1
Makino, H1
Washington, JL1
Pitts, D1
Wright, CG1
Erway, LC1
Davis, RR1
Alagramam, K1
Liao, Z1
Tao, Z1
Hu, L1
Wu, G1
Lan, J1
Ji, J1
Wu, J1
Ji, Y1
Feng, J1
Chen, J1
Li, Z1
Manouvrier, S1
Rötig, A1
Hannebique, G1
Gheerbrandt, JD1
Royer-Legrain, G1
Munnich, A1
Parent, M1
Grünfeld, JP1
Largilliere, C1
Lombes, A1
Velho, G1
Byrne, MM1
Clément, K1
Sturis, J1
Pueyo, ME1
Blanché, H1
Vionnet, N1
Fiet, J1
Passa, P1
Robert, JJ1
Polonsky, KS1
Froguel, P1
Smith, PR1
Bain, SC1
Good, PA1
Hattersley, AT1
Barnett, AH1
Gibson, JM1
Dodson, PM1
Latkany, P1
Ciulla, TA1
Cacchillo, PF1
Malkoff, MD1
Maassen, JA1
van den Ouweland, JM1
Losekoot, M1
Lemkes, HH1

Reviews

1 review available for adenine and Deafness

ArticleYear
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
    Nederlands tijdschrift voor geneeskunde, 2001, Jun-16, Volume: 145, Issue:24

    Topics: Adenine; Adult; Deafness; Diabetes Complications; Diabetes Mellitus; DNA, Mitochondrial; Female; Gua

2001

Other Studies

10 other studies available for adenine and Deafness

ArticleYear
Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation.
    BMC medical genetics, 2015, Oct-08, Volume: 16

    Topics: Adenine; Adolescent; Adult; Age of Onset; Aged; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondr

2015
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Pharmacogenetics and genomics, 2008, Volume: 18, Issue:12

    Topics: Adenine; Aminoacylation; Aminoglycosides; Asian People; Base Sequence; Cell Line; China; Connexin 26

2008
A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.
    BMC medical genetics, 2010, Sep-07, Volume: 11

    Topics: Adenine; Aminoglycosides; Asian People; China; Connexin 26; Connexins; Deafness; DNA Mutational Anal

2010
Pelvic lymphocyst infection associated with maternally inherited diabetes mellitus.
    Diabetes research and clinical practice, 2003, Volume: 61, Issue:2

    Topics: Abdominal Pain; Adenine; Cysts; Deafness; Diabetes Complications; Diabetes Mellitus; DNA, Mitochondr

2003
Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
    Hearing research, 2005, Volume: 202, Issue:1-2

    Topics: Acoustic Stimulation; Adenine; Alleles; Animals; Auditory Threshold; Base Sequence; Cadherin Related

2005
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Gene, 2007, May-15, Volume: 393, Issue:1-2

    Topics: Adenine; Adolescent; Adult; Aminoglycosides; Asian People; Child; China; Connexin 26; Connexins; Dea

2007
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.
    Journal of medical genetics, 1995, Volume: 32, Issue:8

    Topics: Adenine; Adult; Cardiomyopathy, Hypertrophic; Deafness; Diabetes Complications; Diabetes Mellitus; F

1995
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
    Diabetes, 1996, Volume: 45, Issue:4

    Topics: Adenine; Adolescent; Adult; Aged; Arginine; Blood Glucose; Body Mass Index; C-Peptide; Child; Child,

1996
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Ophthalmology, 1999, Volume: 106, Issue:6

    Topics: Adenine; Adult; Aged; Aged, 80 and over; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; El

1999
Mitochondrial maculopathy: geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation.
    American journal of ophthalmology, 1999, Volume: 128, Issue:1

    Topics: Adenine; Atrophy; Deafness; DNA, Mitochondrial; Electroretinography; Female; Guanine; Humans; Macula

1999