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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "One hundred patients with type 2 diabetes and one hundred healthy control subjects were recruited to participate in the study." | 1.42 | Analysis 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." | 1.32 | Pelvic 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." | 1.29 | Clinical 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) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (36.36) | 18.2507 |
| 2000's | 5 (45.45) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhou, MC | 1 |
| Min, R | 1 |
| Ji, JJ | 1 |
| Zhang, S | 1 |
| Tong, AL | 1 |
| Xu, JP | 1 |
| Li, ZY | 1 |
| Zhang, HB | 1 |
| Li, YX | 1 |
| Wang, X | 2 |
| Lu, J | 2 |
| Zhu, Y | 2 |
| Yang, A | 1 |
| Yang, L | 2 |
| Li, R | 1 |
| Chen, B | 1 |
| Qian, Y | 2 |
| Tang, X | 2 |
| Wang, J | 2 |
| Zhang, X | 2 |
| Guan, MX | 2 |
| Bai, Y | 1 |
| Wang, Z | 1 |
| Dai, W | 1 |
| Li, Q | 1 |
| Chen, G | 1 |
| Cong, N | 1 |
| Guan, M | 1 |
| Li, H | 1 |
| Ogawa, D | 1 |
| Shikata, K | 1 |
| Matsuda, M | 1 |
| Wada, J | 1 |
| Uchida, H | 1 |
| Asada, M | 1 |
| Makino, H | 1 |
| Washington, JL | 1 |
| Pitts, D | 1 |
| Wright, CG | 1 |
| Erway, LC | 1 |
| Davis, RR | 1 |
| Alagramam, K | 1 |
| Liao, Z | 1 |
| Tao, Z | 1 |
| Hu, L | 1 |
| Wu, G | 1 |
| Lan, J | 1 |
| Ji, J | 1 |
| Wu, J | 1 |
| Ji, Y | 1 |
| Feng, J | 1 |
| Chen, J | 1 |
| Li, Z | 1 |
| Manouvrier, S | 1 |
| Rötig, A | 1 |
| Hannebique, G | 1 |
| Gheerbrandt, JD | 1 |
| Royer-Legrain, G | 1 |
| Munnich, A | 1 |
| Parent, M | 1 |
| Grünfeld, JP | 1 |
| Largilliere, C | 1 |
| Lombes, A | 1 |
| Velho, G | 1 |
| Byrne, MM | 1 |
| Clément, K | 1 |
| Sturis, J | 1 |
| Pueyo, ME | 1 |
| Blanché, H | 1 |
| Vionnet, N | 1 |
| Fiet, J | 1 |
| Passa, P | 1 |
| Robert, JJ | 1 |
| Polonsky, KS | 1 |
| Froguel, P | 1 |
| Smith, PR | 1 |
| Bain, SC | 1 |
| Good, PA | 1 |
| Hattersley, AT | 1 |
| Barnett, AH | 1 |
| Gibson, JM | 1 |
| Dodson, PM | 1 |
| Latkany, P | 1 |
| Ciulla, TA | 1 |
| Cacchillo, PF | 1 |
| Malkoff, MD | 1 |
| Maassen, JA | 1 |
| van den Ouweland, JM | 1 |
| Losekoot, M | 1 |
| Lemkes, HH | 1 |
1 review available for adenine and Deafness
| Article | Year |
|---|---|
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
Topics: Adenine; Adult; Deafness; Diabetes Complications; Diabetes Mellitus; DNA, Mitochondrial; Female; Gua | 2001 |
10 other studies available for adenine and Deafness
| Article | Year |
|---|---|
Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation.
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.
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.
Topics: Adenine; Aminoglycosides; Asian People; China; Connexin 26; Connexins; Deafness; DNA Mutational Anal | 2010 |
Pelvic lymphocyst infection associated with maternally inherited diabetes mellitus.
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.
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.
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.
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.
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.
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.
Topics: Adenine; Atrophy; Deafness; DNA, Mitochondrial; Electroretinography; Female; Guanine; Humans; Macula | 1999 |