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

作者信息

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

机构信息

Université Paris-Saclay, Inserm UMR996, Inflammation, Microbiome and Immunosurveillance.

Sorbonne Université, Service d'Hémato-oncologie Pédiatrique, Assistance Publique-Hopitaux de Paris (AP-HP), Hôpital Trousseau.

出版信息

Haematologica. 2022 Mar 1;107(3):765-769. doi: 10.3324/haematol.2021.279254.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388e/8883555/455253a27222/107765.fig1.jpg

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本文引用的文献

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Structural basis of CXC chemokine receptor 2 activation and signalling.
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Differential activation and regulation of CXCR1 and CXCR2 by CXCL8 monomer and dimer.
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