biotin has been researched along with Genetic Predisposition in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 5 (55.56) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bindoff, LA; Dölle, C; Flønes, I; Haugarvoll, K; Johansson, S; Jonassen, I; Knappskog, PM; Lykouri, M; Miletic, H; Schwarzlmüller, T; Sztromwasser, P; Tzoulis, C | 1 |
| Bailey, SM; Chatham, JC; Chow, CW; Hamm, JA; He, L; McGinnis, GR; Peliciari-Garcia, RA; Reddy, A; Rowe, GC; Sams, D; Young, ME | 1 |
| Al Hassnan, ZN; Ali, A; Chedrawi, AK; Faiyaz-Ul-Haque, M; Wolf, B | 1 |
| Bellanger, A; Brice, A; Debs, R; Degos, B; Depienne, C; Galanaud, D; Keren, B; Lyon-Caen, O; Rastetter, A; Sedel, F | 1 |
| Guthenberg, C; Holme, E; Ohlsson, A; von Döbeln, U | 1 |
| Angelillo-Scherrer, A; Borgel, D; Brisset, A; Burnier, L; Capron, C; Chanson, M; Chassot, A; Fontana, P; Kwak, BR; Morel, S; Nolli, S; Roth, I; Saller, F; Sugamele, R; Sutter, E | 1 |
| Ettinger, RA; Kwok, WW; Moustakas, AK; Nepom, GT; Papadopoulos, GK | 1 |
| Furukawa, Y; Horiuchi, K; Kamiyama, S; Komai, M; Ohinata, K; Shirakawa, H; Watanabe-Kamiyama, M | 1 |
| Fucharoen, S; Pattanapanyasat, K; Tachavanich, K; Tongtawe, P; Walsh, DS; Wanachiwanawin, W; Yongvanitchit, K | 1 |
9 other study(ies) available for biotin and Genetic Predisposition
| Article | Year |
|---|---|
Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy.
Topics: 5' Untranslated Regions; Adolescent; Alleles; Basal Ganglia; Basal Ganglia Diseases; Biotin; Brain; Exome; Fatal Outcome; Female; Gene Deletion; Gene Silencing; Genetic Predisposition to Disease; Heterozygote; Humans; Male; Membrane Transport Proteins; Mutation; Phenotype; Promoter Regions, Genetic; Sequence Analysis, DNA; Siblings; Thiamine; Young Adult | 2016 |
Biotinylation: a novel posttranslational modification linking cell autonomous circadian clocks with metabolism.
Topics: Acetyl-CoA Carboxylase; Animals; ARNTL Transcription Factors; Biotin; Biotinylation; Carbon-Carbon Ligases; Carbon-Carbon Lyases; Chronobiology Disorders; Circadian Clocks; CLOCK Proteins; Disease Models, Animal; Energy Metabolism; Genetic Predisposition to Disease; Heart Diseases; Liver; Male; Methylmalonyl-CoA Decarboxylase; Mice, Inbred C57BL; Mice, Knockout; Mutation; Myocytes, Cardiac; Phenotype; Protein Processing, Post-Translational; Pyruvate Carboxylase; Symporters; Time Factors | 2016 |
Profound biotinidase deficiency in a child with predominantly spinal cord disease.
Topics: Biotin; Biotinidase Deficiency; Child, Preschool; DNA Mutational Analysis; Early Diagnosis; Gene Expression Regulation, Enzymologic; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Mutation, Missense; Paraparesis, Tropical Spastic; Spinal Cord; Spinal Cord Diseases; Treatment Outcome | 2008 |
Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations.
Topics: Adult; Basal Ganglia; Basal Ganglia Diseases; Biotin; Brain Diseases, Metabolic; DNA Mutational Analysis; Dystonia; Epilepsy; Europe; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Portugal; Thiamine; Treatment Outcome; Vitamin B Complex; White People | 2010 |
Profound biotinidase deficiency: a rare disease among native Swedes.
Topics: Adult; Aminoquinolines; Biomarkers; Biotin; Biotinidase; Biotinidase Deficiency; Child; Child, Preschool; Dietary Supplements; DNA Mutational Analysis; Dried Blood Spot Testing; Emigrants and Immigrants; Genetic Predisposition to Disease; Genetic Testing; Humans; Incidence; Infant; Infant, Newborn; Mutation; Neonatal Screening; Pedigree; Phenotype; Polymorphism, Genetic; Severity of Illness Index; Substrate Specificity; Sweden; Time Factors; Treatment Outcome | 2010 |
Connexin 37 limits thrombus propensity by downregulating platelet reactivity.
Topics: Adolescent; Adult; Animals; Biotin; Bleeding Time; Blood Platelets; Connexins; Down-Regulation; Gap Junction alpha-4 Protein; Gap Junctions; Genetic Predisposition to Disease; Humans; Male; Megakaryocytes; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Platelet Aggregation; Polymorphism, Genetic; Thrombosis; Young Adult | 2011 |
Allelic variation in key peptide-binding pockets discriminates between closely related diabetes-protective and diabetes-susceptible HLA-DQB1*06 alleles.
Topics: Alleles; Amino Acid Motifs; Autoantigens; Binding Sites; Biotin; Cell Line, Transformed; Diabetes Mellitus, Type 1; Genetic Predisposition to Disease; Genetic Variation; Glutamate Decarboxylase; HLA-DQ Antigens; HLA-DQ beta-Chains; Humans; Insulin; Isoenzymes; Membrane Glycoproteins; Membrane Proteins; Models, Molecular; Peptide Fragments; Proinsulin; Protein Binding; Protein Structure, Tertiary; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Protein Tyrosine Phosphatases; Receptor-Like Protein Tyrosine Phosphatases, Class 8 | 2006 |
Antihypertensive effect of biotin in stroke-prone spontaneously hypertensive rats.
Topics: Animals; Biotin; Coronary Vessels; Genetic Predisposition to Disease; Glucose Tolerance Test; Guanylate Cyclase; Hypertension; Male; NG-Nitroarginine Methyl Ester; Nitric Oxide Synthase; Oxadiazoles; Quinoxalines; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Stroke; Time; Vitamins | 2008 |
Impairment of Plasmodium falciparum growth in thalassemic red blood cells: further evidence by using biotin labeling and flow cytometry.
Topics: alpha-Thalassemia; Animals; beta-Thalassemia; Biotin; Erythrocytes; Flow Cytometry; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; In Vitro Techniques; Malaria, Falciparum; Plasmodium falciparum; Reproduction; Splenectomy | 1999 |