T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6-Reference-Cited by-同舟云学术

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T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6

Published:2010-05-05 Issue:4 Volume:55 Page:722-724
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr. Blood Cancer

Author:

Chao Mwe Mwe,Todd Matthew A.,Kontny Udo,Neas Katherine,Sullivan Michael J.,Hunter Alasdair G.,Picketts David J.,Kratz Christian P.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.22574/fullpdf

Reference13 articles.

1. Germline KRAS mutations cause Noonan syndrome;Schubbert;Nat Genet,2006

2. Germline mutations in HRAS proto-oncogene cause Costello syndrome;Aoki;Nat Genet,2005

3. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome;Liaw;Nat Genet,1997

4. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia;Song;Nat Genet,1999

5. Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1;Nichols;Nat Genet,2000

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1. PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS;EMBO Reports;2024-03-01

2. Börjeson–Forssman–Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families;European Journal of Human Genetics;2023-09-14

3. PHF6 maintains acute myeloid leukemia via regulating NF-κB signaling pathway;Leukemia;2023-07-01

4. The chromatin reader PHF6 at the crossroad of the replication stress and DNA damage responses in neuroblastoma through interaction with RRM2;2023-03-10

5. PHF6 promotes the progression of endometrial carcinoma by increasing cancer cells growth and decreasing T‐cell infiltration;Journal of Cellular and Molecular Medicine;2023-02-08

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