thymine has been researched along with Chronic Disease in 18 studies
Chronic Disease: Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2).
| Excerpt | Relevance | Reference |
|---|---|---|
| "We recently identified a single R117H mutation in the cationic trypsinogen gene in several kindreds with an inherited form of acute and chronic pancreatitis (HP1), providing strong evidence that trypsin plays a central role in premature zymogen activation and pancreatitis." | 7.69 | Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis. ( Aston, CE; Ehrlich, GD; Furey, W; Gabbaizedeh, D; Gates, LK; Gorry, MC; Preston, RA; Ulrich, C; Whitcomb, DC; Zhang, Y, 1997) |
| "Glucose-galactose malabsorption (GGM) is a rare autosomal recessive disorder of intestinal transport of glucose and galactose, leading to watery diarrhea, dehydration, failure to thrive, or early death." | 3.72 | Nephrolithiasis in a child with glucose-galactose malabsorption. ( Blau, N; Santer, R; Slaveska, N; Tasic, V, 2004) |
| "We recently identified a single R117H mutation in the cationic trypsinogen gene in several kindreds with an inherited form of acute and chronic pancreatitis (HP1), providing strong evidence that trypsin plays a central role in premature zymogen activation and pancreatitis." | 3.69 | Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis. ( Aston, CE; Ehrlich, GD; Furey, W; Gabbaizedeh, D; Gates, LK; Gorry, MC; Preston, RA; Ulrich, C; Whitcomb, DC; Zhang, Y, 1997) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (16.67) | 18.7374 |
| 1990's | 2 (11.11) | 18.2507 |
| 2000's | 12 (66.67) | 29.6817 |
| 2010's | 1 (5.56) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yilmaz, E | 1 |
| Mir, S | 1 |
| Berdeli, A | 1 |
| SPIES, TD | 1 |
| VILTER, CF | 1 |
| Dirschnabel, AJ | 1 |
| Alvim-Pereira, F | 1 |
| Alvim-Pereira, CC | 1 |
| Bernardino, JF | 1 |
| Rosa, EA | 1 |
| Trevilatto, PC | 5 |
| Scarel-Caminaga, RM | 4 |
| Souza, AP | 3 |
| Brito, RB | 3 |
| Line, SR | 4 |
| de Souza, AP | 1 |
| de Brito, RB | 1 |
| Tasic, V | 1 |
| Slaveska, N | 1 |
| Blau, N | 1 |
| Santer, R | 1 |
| Camargo, LE | 1 |
| Shimada, Y | 1 |
| Tai, H | 1 |
| Endo, M | 1 |
| Kobayashi, T | 1 |
| Akazawa, K | 1 |
| Yamazaki, K | 1 |
| Yacoub, MH | 1 |
| Yuen, AH | 1 |
| Kalsi, KK | 1 |
| Birks, EJ | 1 |
| Taegtmeyer, A | 1 |
| Barton, PJ | 1 |
| Johnson, PH | 1 |
| Suzuki, K | 1 |
| Smolenski, RT | 1 |
| Kedar, PS | 1 |
| Nadkarni, AH | 1 |
| Phanasgoankar, S | 1 |
| Madkaikar, M | 1 |
| Ghosh, K | 1 |
| Gorakshakar, AC | 1 |
| Colah, RB | 1 |
| Mohanty, D | 1 |
| Holla, LI | 1 |
| Fassmann, A | 1 |
| Muzík, J | 1 |
| Vanek, J | 1 |
| Vasku, A | 1 |
| Moreira, PR | 1 |
| Costa, JE | 1 |
| Gomez, RS | 1 |
| Gollob, KJ | 1 |
| Dutra, WO | 1 |
| Goteiner, D | 1 |
| Ashmen, R | 1 |
| Lehrman, N | 1 |
| Janal, MN | 1 |
| Eskin, B | 1 |
| Coon, H | 1 |
| Hoff, M | 1 |
| Holik, J | 1 |
| Delisi, LE | 1 |
| Crowe, T | 1 |
| Freedman, R | 1 |
| Shields, G | 1 |
| Boccio, AM | 1 |
| Lerman, M | 1 |
| Gershon, ES | 1 |
| Gorry, MC | 1 |
| Gabbaizedeh, D | 1 |
| Furey, W | 1 |
| Gates, LK | 1 |
| Preston, RA | 1 |
| Aston, CE | 1 |
| Zhang, Y | 1 |
| Ulrich, C | 1 |
| Ehrlich, GD | 1 |
| Whitcomb, DC | 1 |
| Fouet, P | 1 |
| Denez, B | 1 |
| Zimmermann, P | 1 |
| Rusakov, VI | 1 |
18 other studies available for thymine and Chronic Disease
| Article | Year |
|---|---|
Endothelial nitric oxide synthase (eNOS) gene polymorphism in early term chronic allograft nephropathy.
Topics: Adolescent; Aspartic Acid; Chronic Disease; DNA; Exons; Female; Genotype; Glutamine; Guanine; Humans | 2009 |
The substitution of thymine for folic acid in the treatment of macrocytic anemias in relapse.
Topics: Anemia; Anemia, Macrocytic; Chronic Disease; Folic Acid; Recurrence; Thymine; Vitamin B Complex; Vit | 1946 |
Analysis of the association of IL1B(C-511T) polymorphism with dental implant loss and the clusterization phenomenon.
Topics: Adult; Aged; Aged, 80 and over; Brazil; Case-Control Studies; Chronic Disease; Cytosine; Dental Impl | 2011 |
Investigation of an IL-2 polymorphism in patients with different levels of chronic periodontitis.
Topics: Adult; Alleles; Base Pairing; Chi-Square Distribution; Chronic Disease; Confidence Intervals; DNA; F | 2002 |
Investigation of IL4 gene polymorphism in individuals with different levels of chronic periodontitis in a Brazilian population.
Topics: Adult; Alleles; Black People; Brazil; Chi-Square Distribution; Chronic Disease; Cytosine; Ethnicity; | 2003 |
Analysis of the TGF-beta1 promoter polymorphism (C-509T) in patients with chronic periodontitis.
Topics: Adult; Alleles; Case-Control Studies; Chronic Disease; Cytosine; Female; Gene Frequency; Genetic Mar | 2003 |
Nephrolithiasis in a child with glucose-galactose malabsorption.
Topics: Amino Acid Transport Systems, Basic; Chronic Disease; Codon, Nonsense; Cytosine; Diarrhea; Female; G | 2004 |
Interleukin 10 gene promoter polymorphisms are associated with chronic periodontitis.
Topics: Adenine; Adult; Chronic Disease; Cytosine; Female; Gene Frequency; Genetic Predisposition to Disease | 2004 |
Association of tumor necrosis factor receptor type 2 +587 gene polymorphism with severe chronic periodontitis.
Topics: Adult; Aged; Alleles; Alveolar Bone Loss; Antigens, CD; Biomarkers; Chronic Disease; Female; Guanine | 2004 |
C34T AMP deaminase 1 gene mutation protects cardiac function in donors.
Topics: AMP Deaminase; Cardiac Output, Low; Chronic Disease; Cytosine; Heart; Humans; Mutation; Thymine; Tis | 2004 |
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.
Topics: Amino Acid Substitution; Child; Chronic Disease; Cyanosis; Cytosine; DNA; Female; Globins; Hemoglobi | 2005 |
Functional polymorphisms in the matrix metalloproteinase-9 gene in relation to severity of chronic periodontitis.
Topics: Adult; Alleles; Case-Control Studies; Chronic Disease; Cytosine; Czech Republic; Female; Gene Freque | 2006 |
The IL1A (-889) gene polymorphism is associated with chronic periodontal disease in a sample of Brazilian individuals.
Topics: Adolescent; Adult; Aged; Alleles; Brazil; Chronic Disease; Cross-Sectional Studies; Cytosine; DNA; F | 2007 |
Presence and significance of interleukin-1 polymorphism in patients who present with acute coronary syndrome, angina, and chronic periodontitis: an epidemiologic pilot study.
Topics: Acute Coronary Syndrome; Age Factors; Alveolar Bone Loss; Angina Pectoris; Chronic Disease; Cytosine | 2008 |
C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families.
Topics: Amyloid beta-Protein Precursor; Base Sequence; Chronic Disease; Codon; Cytosine; DNA; Genetic Linkag | 1993 |
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
Topics: Acute Disease; Adenine; Asparagine; Chromosome Mapping; Chromosomes, Human, Pair 7; Chronic Disease; | 1997 |
[Use of Thymobiol in the treatment of chronic ulcerations of the digestive tract].
Topics: Aged; Aluminum Hydroxide; Chronic Disease; Drug Evaluation; Drug Evaluation, Preclinical; Esophagiti | 1976 |
[Use of methyluracyl and pentoxyl in surgery].
Topics: Acute Disease; Appendicitis; Chronic Disease; Humans; Pancreatitis; Postoperative Care; Stomach Dise | 1972 |