✦ LIBER ✦

131 Duplication of DER(8)t(8:12)(q12:p13) and loss of ETV6 gene in a patient with refractory anaemia

✍ Scribed by J.M. Hernández; J.L. García; N. Gutiérrez; M.A. Sánchez; M.B. González; S. Muntión; A. Ríos; J.F.San Miguel

Book ID: 114119325
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 133 KB
Volume: 21
Category: Article
ISSN: 0145-2126
DOI: 10.1016/s0145-2126(97)81346-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of a SRC-like tyrosine ki

Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation

✍ Noriko Hosoya; Ying Qiao; Akira Hangaishi; Lili Wang; Yasuhito Nannya; Masashi S 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 637 KB

## Abstract The SRC family of kinases is rarely mutated in primary human tumors. We report the identification of a SRC‐like tyrosine kinase gene, __FRK__ (Fyn‐related kinase), fused with __ETV6__ in a patient with acute myelogenous leukemia carrying t(6;12)(q21;p13). Both reciprocal fusion transcri

A child with ALL and ETV6/AML1 fusion on

A child with ALL and ETV6/AML1 fusion on a chromosome 12 due to an insertion of AML1 and loss of ETV6 from the homolog involved in a t(12;15)(p13;q15)

✍ Kavita S. Reddy; Xiaojing Yang; Lucia Mak; Shirong Wang; Martin Johnston 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 212 KB 👁 3 views

Identification of a novel fusion gene, T

Identification of a novel fusion gene, TTL, fused to ETV6 in acute lymphoblastic leukemia with t(12;13)(p13;q14), and its implication in leukemogenesis

✍ Qiao, Y; Ogawa, S; Hangaishi, A; Yuji, K; Izutsu, K; Kunisato, A; Imai, Y; Wang, 📂 Article 📅 2003 🏛 Nature Publishing Group 🌐 English ⚖ 338 KB

Fusion of TEL/ETV6 to a novel ACS2 in my

Fusion of TEL/ETV6 to a novel ACS2 in myelodysplastic syndrome and acute myelogenous leukemia with t(5;12)(q31;p13)

✍ Fumiharu Yagasaki; Itsuro Jinnai; Satoru Yoshida; Yasuko Yokoyama; Akira Matsuda 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 496 KB 👁 3 views

We identified a novel human long fatty acyl CoA synthetase 2 gene, ACS2, as a new ETV6 fusion partner gene in a recurrent t(5;12)(q31;p13) translocation in a patient with refractory anemia with excess blasts (RAEB) with basophilia, a patient with acute myelogenous leukemia (AML) with eosinophilia, a

Characterization of the breakpoints in a

Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization

✍ Olga Chernova; Ivan Still; Matt Kalaycio; Gerald Hoeltge; John K. Cowell 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB 👁 1 views

We used fluorescence in situ hybridization to characterize the molecular position of the breakpoints in a t(8;13)(p11;q12) reciprocal translocation from a patient with an atypical myeloproliferative disorder. This structural chromosome abnormality is characteristic of this specific disease and occur

Cryptic t(12;15)(p13;q26) producing the

Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11: fluorescence in situ hybridization and IGF2 allelic expression analysis

✍ Naoki Watanabe; Hirofumi Kobayashi; Toshinori Hirama; Atsushi Kikuta; Shoichi Ko 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 517 KB