Protein Tyrosine Phosphatase SHP-2 (PTPN11)‎ in Hematopoiesis and Leukemogenesis

المؤلفون المشاركون

Qu, Cheng-Kui
Liu, Xia

المصدر

Journal of Signal Transduction

العدد

المجلد 2011، العدد 2011 (31 ديسمبر/كانون الأول 2011)، ص ص. 1-8، 8ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2011-06-07

دولة النشر

مصر

عدد الصفحات

8

التخصصات الرئيسية

الأحياء

الملخص EN

SHP-2 (PTPN11), a ubiquitously expressed protein tyrosine phosphatase, is critical for hematopoietic cell development and function owing to its essential role in growth factor/cytokine signaling.

More importantly, germline and somatic mutations in this phosphatase are associated with Noonan syndrome, Leopard syndrome, and childhood hematologic malignancies.

The molecular mechanisms by which SHP-2 mutations induce these diseases are not fully understood, as the biochemical bases of SHP-2 functions still remain elusive.

Further understanding SHP-2 signaling activities and identification of its interacting proteins/substrates will shed light on the pathogenesis of PTPN11-associated hematologic malignancies, which, in turn, may lead to novel therapeutics for these diseases.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Liu, Xia& Qu, Cheng-Kui. 2011. Protein Tyrosine Phosphatase SHP-2 (PTPN11) in Hematopoiesis and Leukemogenesis. Journal of Signal Transduction،Vol. 2011, no. 2011, pp.1-8.
https://search.emarefa.net/detail/BIM-453587

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Liu, Xia& Qu, Cheng-Kui. Protein Tyrosine Phosphatase SHP-2 (PTPN11) in Hematopoiesis and Leukemogenesis. Journal of Signal Transduction No. 2011 (2011), pp.1-8.
https://search.emarefa.net/detail/BIM-453587

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Liu, Xia& Qu, Cheng-Kui. Protein Tyrosine Phosphatase SHP-2 (PTPN11) in Hematopoiesis and Leukemogenesis. Journal of Signal Transduction. 2011. Vol. 2011, no. 2011, pp.1-8.
https://search.emarefa.net/detail/BIM-453587

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-453587