Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Janan Ghalib, Hasan"'
Autor:
Janan Ghalib Hasan, Ahmed Mohsin Aziz
Publikováno v:
Journal of Radiology and Oncology. :022-035
Autor:
Kazuyuki Matsuda, Tingting Liu, Lika’a Fasih Y. Al-Kzayer, Jaafar M.H. Abdulkadhim, Hussam M. Salih Al-Abdullah, Kenichi Koike, Janan Ghalib Hasan, Le T.N. Uyen, Zead Ismael I.K. Matti, Tariq Abadi Al-Shujairi, Kazuo Sakashita, Salma Abbas Al-Hadad, Toshi Inoshita, Faris Madanat, Minoru Kamata, Maher A. Sughayer, Mazin Faisal Al-Jadiry
Publikováno v:
Pediatric Blood & Cancer. 61:1980-1985
Background. RUNX1 mutation plays an important role in adult leukemic transformation. However, its contribution to the development of childhood leukemia remains unclear. In the present study, we analyzed point mutations of RUNX1 gene in children and a
Autor:
Jaafar M.H. Abdulkadhim, Lika’a Fasih Y. Al-Kzayer, Le T.N. Uyen, M. Al-Ani, Hasanein H. Ghali, Salma Abbas Al-Hadad, Tariq Abadi Al-Shujairi, Zead Ismael I.K. Matti, Najiha Ahmed Ameen, Mazin Faisal Al-Jadiry, Toshi Inoshita, Paiman Ali I. Saber, Hussam M. Salih Al-Abdullah, Kenichi Koike, Hisham Maree Khalil, Janan Ghalib Hasan, Safaa A. F. Al‐Badri, Kazuyuki Matsuda, Minoru Kamata, Tingting Liu, Kazuo Sakashita
Publikováno v:
Annals of Hematology. 93:949-955
The lack of molecular diagnosis in the field of cancer in Iraq has motivated us to perform a genetic analysis of pediatric acute myelogenous leukemia (AML), including class I and II aberrations. Peripheral blood or bone marrow cells were collected fr
Frequent coexistence of RAS mutations in RUNX1-mutated acute myeloid leukemia in Arab Asian children
Autor:
Lika'a Fasih Y, Al-Kzayer, Kazuo, Sakashita, Mazin Faisal, Al-Jadiry, Salma Abbas, Al-Hadad, Le T N, Uyen, Tingting, Liu, Kazuyuki, Matsuda, Jaafar M H, Abdulkadhim, Tariq Abadi, Al-Shujairi, Zead Ismael I K, Matti, Janan Ghalib, Hasan, Hussam M Salih, Al-Abdullah, Toshi, Inoshita, Minoru, Kamata, Maher A, Sughayer, Faris F, Madanat, Kenichi, Koike
Publikováno v:
Pediatric bloodcancer. 61(11)
RUNX1 mutation plays an important role in adult leukemic transformation. However, its contribution to the development of childhood leukemia remains unclear. In the present study, we analyzed point mutations of RUNX1 gene in children and adolescents w
Autor:
Lika’a Fasih Y. Al-Kzayer, Jaafar M.H. Abdulkadhim, Kenichi Koike, M. Al-Ani, Janan Ghalib Hasan, Hussam M. Salih Al-Abdullah, Mazin Faisal Al-Jadiry, Paiman Ali I. Saber, Tariq Abadi Al-Shujairi, Kazuo Sakashita, Salma Abbas Al-Hadad, Kazuyuki Matsuda, Toshi Inoshita, Minoru Kamata, Wisam Majeed Abed
Publikováno v:
Pediatric bloodcancer. 59(3)
Background Genetic examination of childhood leukemia has not been available in Iraq. We here report the frequency of TEL-AML1, E2A-PBX1, MLL-AF4, and BCR-ABL chimeric transcripts in 264 Iraqi children newly diagnosed with acute lymphoblastic leukemia