International Journal of Clinical Medicine

International Journal of Clinical Medicine

ISSN Print: 2158-284X
ISSN Online: 2158-2882
www.scirp.org/journal/ijcm
E-mail: ijcm@scirp.org
"Hereditary Leukemia Due to Rare RUNX1c Splice Variant (L472X) Presents with Eczematous Phenotype"
written by April Sorrell, Carin Espenschied, Wei Wang, Jeffrey Weitzel, Su Chu, Pablo Parker, Juan-Sebastian Saldivar, Ravi Bhatia,
published by International Journal of Clinical Medicine, Vol.3 No.7, 2012
has been cited by the following article(s):
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[1] Molecular basis of haematological disease caused by inherited or acquired RUNX1 mutations
Experimental …, 2022
[2] Conduite à tenir devant une prédisposition génétique aux hémopathies malignes chez un patient candidat à l'allogreffe de cellules souches hématopoïétiques (CSH) …
Bulletin du …, 2022
[3] Defining Leukemogenic Mechanisms in Hereditary Hematopoietic Malignancies
2021
[4] Mutations/délétions germinales de RUNX1 et prédisposition génétique aux hémopathies malignes
2021
[5] Genetic Predisposition to Myelodysplastic Syndrome in Clinical Practice
2020
[6] Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA)
2020
[7] RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
2020
[8] Runx1 negatively regulates inflammatory cytokine production by neutrophils in response to Toll-like receptor signaling
2020
[9] RUNX1 変異による家族性白血病研究 20 年の成果と今後の課題
2020
[10] Familial acute myeloid leukemia
2020
[11] Progressive pigmented purpuric dermatosis and platelet delta storage pool deficiency in a child
2019
[12] The Road to Pathogenesis: Charting the Development of LSCs and Pre-LSCs
2019
[13] The VWRPY Domain is Essential for RUNX1 Function in Hematopoietic Progenitor Cell Maturation and Megakaryocyte Differentiation.
2018
[14] Bone marrow pathologic abnormalities in familial platelet disorder with propensity for myeloid malignancy and germline RUNX1 mutation
2017
[15] Recognition of familial myeloid neoplasia in adults
Seminars in Hematology, 2017
[16] Role of RUNX1 in hematological malignancies
2017
[17] RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)
Seminars in Hematology, 2017
[18] RUNX1 Mutations in Inherited and Sporadic Leukemia
Frontiers in Cell and Developmental Biology, 2017
[19] 急性髓系白血病相关基因的 DNA 甲基化
中国细胞生物学学报, 2015
[20] Novel germline DDX41 mutations define families with a lower age of MDS/AML onset, and lymphoid malignancies
Blood, 2015
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