tyrosine and Familial Turner Syndrome

tyrosine has been researched along with Familial Turner Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chan, RJ; Chen, H; Fu, XY; He, Y; Luo, Y; Miller, LC; Moh, A; Payne, RM; Shou, W; Yang, Z; Yin, F; Zhang, W; Zhang, X; Zhang, ZY	1

Other Studies

1 other study(ies) available for tyrosine and Familial Turner Syndrome

Article	Year
Negative regulation of Stat3 by activating PTPN11 mutants contributes to the pathogenesis of Noonan syndrome and juvenile myelomonocytic leukemia. The Journal of biological chemistry, 2009, Aug-14, Volume: 284, Issue:33 Topics: Animals; Flow Cytometry; Gene Expression Regulation, Leukemic; Humans; Leukemia, Myelomonocytic, Juvenile; Mice; Models, Biological; Mutation; Noonan Syndrome; Protein Tyrosine Phosphatase, Non-Receptor Type 11; STAT3 Transcription Factor; Tyrosine	2009

Article

Year

Negative regulation of Stat3 by activating PTPN11 mutants contributes to the pathogenesis of Noonan syndrome and juvenile myelomonocytic leukemia.

The Journal of biological chemistry, 2009, Aug-14, Volume: 284, Issue:33

Topics: Animals; Flow Cytometry; Gene Expression Regulation, Leukemic; Humans; Leukemia, Myelomonocytic, Juvenile; Mice; Models, Biological; Mutation; Noonan Syndrome; Protein Tyrosine Phosphatase, Non-Receptor Type 11; STAT3 Transcription Factor; Tyrosine

2009