Constitutional t(16;21)(p13;q22) as a novel pathogenomic mechanism in a series of three new RUNX1 mutated FPD/AML pedigrees: implications for diagnostics

被引：0

作者：

Buijs, Arjan ^{[1
]}

van der Crabben, Saskia ^{[1
]}

van der Zwaag, Bert ^{[1
]}

van Binsbergen, Ellen ^{[1
]}

Poot, Martin ^{[1
]}

de Weerdt, Okke ^{[2
]}

van Gijn, Marielle ^{[1
]}

Nieuwenhuis, Karel ^{[3
]}

机构：

[1] Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands

[2] St Antonius Hosp, Dept Internal Med, Nieuwegein, Netherlands

[3] Univ Med Ctr Utrecht, Dept Hematol, Utrecht, Netherlands

来源：

CHROMOSOME RESEARCH | 2011年 / 19卷

关键词：

constitutional translocation; RUNX1; ATF7IP2; FPD/AML;

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

6.O1

引用

页码：S30 / S30

页数：1

共 41 条

[1] Constitutional t(16;21)(p13;q22) Identified by FISH and Next-Generation Genome-Wide Long Mate-Pair Sequencing Analysis as a Novel Pathogenomic Mechanism in a Series of Three New RUNX1 Mutated FPD/AML Pedigrees: Implications for Diagnostics
Buijs, A.
Poot, M.
van der Crabben, S.
van der Zwaag, B.
van Binsbergen, E.
van Roosmalen, M. J.
Tavakoli-Yaraki, M.
de Weerdt, O.
Nieuwenhuis, H. K.
van Gijn, M.
Kloosterman, W. P.
CYTOGENETIC AND GENOME RESEARCH, 2012, 136 (04) : 336 - 337
[2] IDENTIFICATION OF A CONSTITUTIONAL T(16;21) INVOLVING 16P13 ATF7IP2 AND 21Q22 RUNX1 LOCI AS A NOVEL GENETIC MECHANISM IN FPD/AML
Buijs, A.
van der Crabben, S.
van der Zwaag, B.
van Binsbergen, E.
Poot, M.
de Weerdt, O.
van Gijn, M.
Nieuwenhuis, K.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 : 86 - 86
[3] Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees
A Buijs
M Poot
S van der Crabben
B van der Zwaag
E van Binsbergen
M J van Roosmalen
M Tavakoli-Yaraki
O de Weerdt
H K Nieuwenhuis
M van Gijn
W P Kloosterman
Leukemia, 2012, 26 : 2151 - 2154
[4] Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees
Buijs, A.
Poot, M.
van der Crabben, S.
van der Zwaag, B.
van Binsbergen, E.
van Roosmalen, M. J.
Tavakoli-Yaraki, M.
de Weerdt, O.
Nieuwenhuis, H. K.
van Gijn, M.
Kloosterman, W. P.
LEUKEMIA, 2012, 26 (09) : 2151 - 2154
[5] Outcome of East Kent patients with AML associated with good risk cytogenetics-t (8;21) (q22;q22), inv(16)(p13;q22)/t(16;16)(p13;q22), and t (15;17)(q22;q21) from AML 15 and 17 trials
Ko, T. Ko
Young, M.
Lindsay, J.
Pocock, C.
BRITISH JOURNAL OF HAEMATOLOGY, 2018, 181 : 159 - 159
[6] Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia
Macke, Erica L.
Meyer, Reid G.
Hoppman, Nicole L.
Ketterling, Rhett P.
Greipp, Patricia T.
Xu, Xinjie
Baughn, Linda B.
Shafer, Danielle A.
He, Rui R.
Peterson, Jess F.
LABORATORY MEDICINE, 2022, 53 (04) : E87 - E90
[7] A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement
Park, Kyoung-Jin
Park, Hyung-Doo
Kim, Hee-Jin
Yoo, Keon Hee
Koo, Hono Hoe
Kim, Sun-Hee
CANCER GENETICS AND CYTOGENETICS, 2009, 192 (02) : 90 - 92
[8] Identification of a novel CBFB/MYH11 fusion in a patient with AML-M1 and a t(16;16)(p13;q22).
Van Limbergen, H
Van der Reijden, B
Poppe, B
Offner, F
Van Roy, N
Dauwerse, H
De Paepe, A
Speleman, F
BLOOD, 1999, 94 (10) : 215B - 215B
[9] A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia
Paulien, S
Maarek, O
Daniel, MT
Berger, R
ANNALES DE GENETIQUE, 2002, 45 (02): : 67 - 69
[10] LRP16 is fused to RUNX1 in monocytic leukemia cell line with t(11;21)(q13;q22)
Imagama, Shizuka
Abe, Akihiro
Suzuki, Momoko
Hayakawa, Fumihiko
Katsumi, Akira
Emi, Nobuhiko
Kiyoi, Hitoshi
Naoe, Tomoki
EUROPEAN JOURNAL OF HAEMATOLOGY, 2007, 79 (01) : 25 - 31

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