✦ LIBER ✦

Defective Expression of Bruton's Tyrosine Kinase in Acute Lymphoblastic Leukemia

✍ Scribed by Goodman, Patricia A.; Wood, Carla M.; Vassilev, Alexei O.; Mao, Chen; Uckun, Fatih M.

Book ID: 120506481
Publisher: Informa plc
Year: 2003
Tongue: English
Weight: 297 KB
Volume: 44
Category: Article
ISSN: 1042-8194
DOI: 10.1080/1042819031000067576

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Transcriptional regulatory defects in th

Transcriptional regulatory defects in the first intron of Bruton’s tyrosine kinase

✍ Dong-Min Shin; Eun-Kyeong Jo; Hirokazu Kanegane; Takeshi Futatani; Meina Zhao; C 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 157 KB

Hypermethylation of the spleen tyrosine

Hypermethylation of the spleen tyrosine kinase promoter in T-lineage acute lymphoblastic leukemia

✍ Goodman, Patricia A; Burkhardt, Nicole; Juran, Brian; Tibbles, Heather E; Uckun, 📂 Article 📅 2003 🏛 Nature Publishing Group 🌐 English ⚖ 310 KB

Managing Philadelphia Chromosome-Positiv

Managing Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: Role of Tyrosine Kinase Inhibitors

✍ Farhad Ravandi 📂 Article 📅 2011 🏛 Elsevier 🌐 English ⚖ 273 KB

Expression of Bruton's tyrosine kinase p

Expression of Bruton's tyrosine kinase protein within the B cell lineage

✍ Helen C. Genevier; Steve Hinshelwood; Hubert B. Gaspar; Kevin P. Rigley; Derek B 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 620 KB

Spleen tyrosine kinase (Syk) deficiency

Spleen tyrosine kinase (Syk) deficiency in childhood pro-B cell acute lymphoblastic leukemia

✍ Goodman, Patricia A; Wood, Carla M; Vassilev, Alexei; Mao, Chen; Uckun, Fatih M 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 665 KB

Molecular analysis of Bruton’s tyrosine

Molecular analysis of Bruton’s tyrosine kinase gene in Spain

✍ Ma Cruz García Rodríguez; Eduardo López Granados; Antonio Ferreira Cerdán; Gumer 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB

Mutations in Bruton´s tyrosine kinase (BTK) gene result in X linked agammaglobulinemia (XLA). Using Single Strand Conformation Polymorphism (SSCP) followed by direct sequencing 21 mutations were found in 27 patients with an XLA phenotype from 21 unrelated families. We identified 13 novel and 8 known