tyrosine and Hirschsprung Disease

tyrosine has been researched along with Hirschsprung Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bendlova, B; Bilek, R; Dvorakova, K; Dvorakova, S; Skaba, R; Sykorova, V; Vaclavikova, E; Vlcek, P; Zelinka, T1
Alberti, L; Arighi, E; Bocciardi, R; Bongarzone, I; Borrello, MG; Greco, A; Luo, Y; Miranda, C; Mondellini, P; Pasini, B1
Carlomagno, F; De Vita, G; Fusco, A; Jing, S; Lupoli, G; Melillo, RM; Salvatore, G; Santoro, M; Vecchio, G; Visconti, R; Yu, Y1
Asai, N; Ito, S; Iwashita, T; Murakami, H; Takahashi, M1

Other Studies

4 other study(ies) available for tyrosine and Hirschsprung Disease

ArticleYear
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest.
    Endocrine, 2009, Volume: 36, Issue:3

    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.
    Nature genetics, 1995, Volume: 10, Issue:1

    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.
    Endocrinology, 1998, Volume: 139, Issue:8

    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.
    Journal of internal medicine, 1998, Volume: 243, Issue:6

    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