Hereditary Leukemia Due to Rare <i>RUNX</i>1c Splice Variant (L472X) Presents with Eczematous Phenotype-Reference-Cited by-同舟云学术

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Hereditary Leukemia Due to Rare <i>RUNX</i>1c Splice Variant (L472X) Presents with Eczematous Phenotype

Published:2012 Issue:07 Volume:03 Page:607-613
ISSN:2158-284X
Container-title:International Journal of Clinical Medicine
language:
Short-container-title:IJCM

Author:

Sorrell April,Espenschied Carin,Wang Wei,Weitzel Jeffrey,Chu Su,Parker Pablo,Saldivar Juan-Sebastian,Bhatia Ravi

Publisher

Scientific Research Publishing, Inc.

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency;Blood Advances;2024-03-29

2. Natural history study of patients with familial platelet disorder with associated myeloid malignancy;Blood;2023-12-21

3. Altered Platelet-Megakaryocyte Endocytosis and Trafficking of Albumin and Fibrinogen inRUNX1Haplodeficiency;2023-10-23

4. RUNX1 is required in granulocyte–monocyte progenitors to attenuate inflammatory cytokine production by neutrophils;Genes & Development;2023-07-01

5. Conduite à tenir devant une prédisposition génétique aux hémopathies malignes chez un patient candidat à l’allogreffe de cellules souches hématopoïétiques (CSH) : recommandations de la SFGM-TC;Bulletin du Cancer;2023-02

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