Page last updated: 2024-10-20

thymine and Cystic Fibrosis

thymine has been researched along with Cystic Fibrosis in 5 studies

Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's3 (60.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dawson, KP2
Frossard, PM2
Al-Awar, B1
Howden, R1
Gelfi, C1
Righetti, PG1
Cremonesi, L1
Ferrari, M1
Witt, M1
Pogorzelski, A1
Zebrak, J1
Rutkiewicz, E1
Hertecant, J1
Bossaert, Y1

Other Studies

5 other studies available for thymine and Cystic Fibrosis

ArticleYear
Disease severity associated with cystic fibrosis mutations deltaF508 and S549R(T-->G).
    Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit, 2001, Volume: 7, Issue:6

    Topics: Amino Acid Substitution; Arabs; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Cystic Fibrosis

2001
A new medium for the isolation of Staphylococcus aureus, including thymine requiring strains, from sputum.
    Medical laboratory sciences, 1981, Volume: 38, Issue:1

    Topics: Agar; Cystic Fibrosis; Humans; Sputum; Staphylococcus aureus; Thymine

1981
Detection of point mutations by capillary electrophoresis in liquid polymers in temporal thermal gradients.
    Electrophoresis, 1994, Volume: 15, Issue:12

    Topics: Adenine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Cytosine; DNA; Electr

1994
A cystic fibrosis patient homozygous for 621 + 1G-->T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal reflux.
    Clinical genetics, 1996, Volume: 50, Issue:3

    Topics: Adult; Bronchitis; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pa

1996
Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T-->G).
    The European respiratory journal, 1999, Volume: 13, Issue:1

    Topics: Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Geno

1999