sapropterin has been researched along with Genetic Predisposition in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (50.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 2 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chedia, AM; Finegold, DN; McClain, LL; Pan, L; Peters, DG; Rengasamy, M; Sabol, R; Segretti, AM; Shaw, P | 1 |
| Anikster, Y; Belanger-Quintana, A; Blau, N; Bonfim-Freitas, PE; Burlina, A; Burton, BK; Carducci, C; Chiesa, AE; Christodoulou, J; Desviat, LR; Eliyahu, A; Evers, RAF; Fajkusova, L; Feillet, F; Garbade, SF; Giżewska, M; Gundorova, P; Hillert, A; Hoffmann, GF; Karall, D; Kneller, K; Kutsev, SI; Leuzzi, V; Levy, HL; Lichter-Konecki, U; Muntau, AC; Namour, F; Oltarzewski, M; Paras, A; Perez, B; Polak, E; Polyakov, AV; Porta, F; Rohrbach, M; Santana-da Silva, LC; Scholl-Bürgi, S; Shen, N; Skouma, A; Spécola, N; Stojiljković, M; Stoppioni, V; Thöny, B; Trefz, FK; van Spronsen, F; Vockley, J; Yu, Y; Zschocke, J; Đorđević, M | 1 |
| Allen, D; Belfer, I; Channon, KM; Cunnington, C; Darbari, DS; Desai, K; Diaw, L; Dizon, M; Freeman, L; Goldman, D; Hartley, SW; Kato, GJ; Milton, J; Nolan, V; Steinberg, MH; Taylor, JG; Wang, Z; Youngblood, V | 1 |
| Dunin-Wilczyńska, I; Hozyasz, KK; Jagodziński, PP; Lasota, A; Mostowska, A; Wójcicki, P; Zadurska, M | 1 |
| Deng, Y; Jia, H; Jin, X; Li, N; Li, X; Liu, Z; Song, J; Tao, J; Zhu, J | 1 |
| Abramson, RK; Anderson, BM; Brown, KD; Cuccaro, ML; Gilbert, JR; Haines, JL; Pericak-Vance, MA; Schnetz-Boutaud, NC; Wright, HH | 1 |
| Channon, KM; Guzik, TJ | 1 |
| Cui, J; DeStefano, AL; Guttman, M; Karamohamed, S; Laramie, JM; Latourelle, JC; McKee, AC; Myers, RH; Tobin, JE; Wilk, JB | 1 |
| Bowling, K; Chaudhuri, A; Funderburk, C; Inamdar, A; Lawal, H; O'Donnell, JM; Wang, Z | 1 |
| Adolph, J; Geisslinger, G; Lötsch, J; Schmidt, H; Tegeder, I; Woolf, CJ | 1 |
1 review(s) available for sapropterin and Genetic Predisposition
| Article | Year |
|---|---|
Mechanisms of superoxide production in human blood vessels: relationship to endothelial dysfunction, clinical and genetic risk factors.
Topics: Alleles; Arteriosclerosis; Biopterins; Blood Vessels; Endothelium, Vascular; Genetic Predisposition to Disease; Humans; Membrane Transport Proteins; NADPH Dehydrogenase; NADPH Oxidases; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Phosphoproteins; Polymorphism, Genetic; Superoxides; Vascular Diseases | 2002 |
9 other study(ies) available for sapropterin and Genetic Predisposition
| Article | Year |
|---|---|
Rare variants and biological pathways identified in treatment-refractory depression.
Topics: Adolescent; Adult; Alleles; Biopterins; Carnitine; Computer Simulation; Depressive Disorder, Treatment-Resistant; Exome Sequencing; Female; Genetic Predisposition to Disease; Humans; Male; Phenotype; Polymorphism, Single Nucleotide; Tetrahydrofolates; Young Adult | 2020 |
The Genetic Landscape and Epidemiology of Phenylketonuria.
Topics: Alleles; Biopterins; Europe; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Mutation; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias | 2020 |
A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia.
Topics: Adult; Alleles; Anemia, Sickle Cell; Biopterins; Case-Control Studies; Endothelium; Female; Gene Expression Regulation; Gene Frequency; Genetic Association Studies; Genetic Markers; Genetic Predisposition to Disease; GTP Cyclohydrolase; Haplotypes; Humans; Male; Middle Aged; Odds Ratio; Pain; Pain Management; Phenotype; Plethysmography; Sex Factors; Transcriptome; Vascular Diseases; Young Adult | 2014 |
Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts.
Topics: Biopterins; Cleft Lip; Cleft Palate; Female; Genetic Predisposition to Disease; Genetic Variation; GTP Cyclohydrolase; Humans; Male; Polymorphism, Single Nucleotide; Risk Factors | 2016 |
Correlation between genotype and the tetrahydrobiopterin-responsive phenotype in Chinese patients with phenylketonuria.
Topics: Asian People; Biopterins; China; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Humans; Mutation; Phenotype; Phenylalanine Hydroxylase; Phenylketonurias; Predictive Value of Tests | 2015 |
Examination of tetrahydrobiopterin pathway genes in autism.
Topics: Adolescent; Autistic Disorder; Biopterins; Brain; Child; Child, Preschool; Chromosomes, Human, Pair 11; DNA Mutational Analysis; Female; Gene Expression Regulation; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Phosphorus-Oxygen Lyases; Polymorphism, Single Nucleotide; Signal Transduction; Young Adult | 2009 |
Sepiapterin reductase expression is increased in Parkinson's disease brain tissue.
Topics: Aged; Alcohol Oxidoreductases; Aldehyde Reductase; Biopterins; Cerebellum; Female; Gene Expression Regulation; Genetic Predisposition to Disease; GTP Cyclohydrolase; Humans; Male; Middle Aged; Parkinson Disease; Phosphorus-Oxygen Lyases; Polymorphism, Single Nucleotide; Reference Values | 2007 |
Interaction of genetic and environmental factors in a Drosophila parkinsonism model.
Topics: Animals; Biopterins; Catalase; Cell Aggregation; Disease Models, Animal; Dopamine; Drosophila; Drosophila Proteins; Dyskinesia, Drug-Induced; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Hazardous Substances; Herbicides; Homeostasis; Longevity; Male; Mutation; Neurons; Paraquat; Parkinsonian Disorders | 2007 |
Reduced hyperalgesia in homozygous carriers of a GTP cyclohydrolase 1 haplotype.
Topics: Adult; Biopterins; Colforsin; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; GTP Cyclohydrolase; Haplotypes; Heterozygote; Homozygote; Humans; Hyperalgesia; Low Back Pain; Male; Neurosurgical Procedures; Pain Measurement; Pain Threshold; Radiculopathy | 2008 |