tyrosine has been researched along with Hirschsprung Disease in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (75.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bendlova, B; Bilek, R; Dvorakova, K; Dvorakova, S; Skaba, R; Sykorova, V; Vaclavikova, E; Vlcek, P; Zelinka, T | 1 |
Alberti, L; Arighi, E; Bocciardi, R; Bongarzone, I; Borrello, MG; Greco, A; Luo, Y; Miranda, C; Mondellini, P; Pasini, B | 1 |
Carlomagno, F; De Vita, G; Fusco, A; Jing, S; Lupoli, G; Melillo, RM; Salvatore, G; Santoro, M; Vecchio, G; Visconti, R; Yu, Y | 1 |
Asai, N; Ito, S; Iwashita, T; Murakami, H; Takahashi, M | 1 |
4 other study(ies) available for tyrosine and Hirschsprung Disease
Article | Year |
---|---|
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Carcinoma, Medullary; Child; Disease; Family; Female; Genetic Association Studies; Germ-Line Mutation; Hirschsprung Disease; Humans; Male; Middle Aged; Multiple Endocrine Neoplasia Type 2a; Neural Crest; Phenylalanine; Polymorphism, Single Nucleotide; Proto-Oncogene Mas; Proto-Oncogene Proteins c-ret; Thyroid Neoplasms; Tyrosine; Young Adult | 2009 |
Loss of function effect of RET mutations causing Hirschsprung disease.
Topics: 3T3 Cells; Animals; Base Sequence; Cell Differentiation; Cell Transformation, Neoplastic; Cyclic AMP-Dependent Protein Kinases; Drosophila Proteins; Exons; Genetic Complementation Test; HeLa Cells; Hirschsprung Disease; Humans; Mice; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; PC12 Cells; Phosphorylation; Precipitin Tests; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-ret; Rats; Receptor Protein-Tyrosine Kinases; Recombinant Fusion Proteins; Transfection; Tyrosine | 1995 |
Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.
Topics: 3T3 Cells; Adaptor Proteins, Signal Transducing; Adaptor Proteins, Vesicular Transport; Animals; Cell Line; Drosophila Proteins; Glial Cell Line-Derived Neurotrophic Factor; Glial Cell Line-Derived Neurotrophic Factor Receptors; Hirschsprung Disease; Humans; Immunosorbent Techniques; Mice; Multiple Endocrine Neoplasia Type 2a; Mutation; Nerve Growth Factors; Nerve Tissue Proteins; Phosphatidylinositol Diacylglycerol-Lyase; Phosphorylation; Proteins; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-ret; Receptor Protein-Tyrosine Kinases; Recombinant Proteins; Shc Signaling Adaptor Proteins; Signal Transduction; Src Homology 2 Domain-Containing, Transforming Protein 1; Transfection; Type C Phospholipases; Tyrosine | 1998 |
Molecular mechanisms of development of multiple endocrine neoplasia 2 by RET mutations.
Topics: Carcinoma, Medullary; Drosophila Proteins; Hirschsprung Disease; Humans; Multiple Endocrine Neoplasia Type 2a; Multiple Endocrine Neoplasia Type 2b; Mutation; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-ret; Receptor Protein-Tyrosine Kinases; Thyroid Neoplasms; Tyrosine | 1998 |