Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity-Reference-Cited by-同舟云学术

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Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity

Published:2021-12-02 Issue: Volume: Page:
ISSN:1592-8721
Container-title:Haematologica
language:
Short-container-title:haematol

Author:

Marin-Esteban Viviana,Youn Jenny,Beaupain Blandine,Jaracz-Ros Agnieszka,Barlogis Vincent,Fenneteau Odile,Leblanc Thierry,Bellanger Florence,Pellet Philippe,Buratti Julien,Lapillonne Hélène,Bachelerie Françoise,Donadieu Jean,Bellanné-Chantelot Christine

Abstract

Not available.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 9 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. Expanding CXCR4 variant landscape in WHIM syndrome: integrating clinical and functional data for variant interpretation;Frontiers in Immunology;2024-07-08

2. The complex nature of CXCR4 mutations in WHIM syndrome;Frontiers in Immunology;2024-07-05

3. Dissecting thrombus-directed chemotaxis and random movement in neutrophil near-thrombus motion in flow chambers;BMC Biology;2024-05-20

4. Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses;Journal of Clinical Pathology;2024-04-08

5. Immune cell networking in solid tumors: focus on macrophages and neutrophils;Frontiers in Immunology;2024-02-14

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