Association of <scp><i>MPL</i> K39N</scp> and <scp>R102P</scp> heterozygous germline mutations lead to hereditary thrombocytosis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Association of MPL K39N and R102P heterozygous germline mutations lead to hereditary thrombocytosis

Published:2024-05-16 Issue:8 Volume:99 Page:1644-1646
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:American J Hematol

Author:

Voirin Emeline¹²,Bouvier Anne¹,Plo Isabelle³,Durix Léa³,Beucher Annaëlle¹,Giraudier Stephane⁴^ORCID,Ugo Valérie¹,Brasme Jean‐François⁵,Luque Paz Damien¹^ORCID

Affiliation:

1. Univ Angers, Nantes Université, CHU Angers, Inserm, CNRS, CRCI2NA Angers France

2. Laboratoire d'Hématologie CHU Tours Tours France

3. INSERM, UMR 1287, Gustave Roussy, Université Paris Saclay Villejuif France

4. Cellular biology Department, Saint‐Louis Hospital, APHP Université Paris Cité Paris France

5. CHU Angers, Unité d'Onco‐Hémato‐Immunologie pédiatrique Angers France

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.27368

Reference6 articles.

1. Genetic Alterations of the Thrombopoietin/MPL/JAK2 Axis Impacting Megakaryopoiesis

2. Mpl Baltimore: A thrombopoietin receptor polymorphism associated with thrombocytosis

3. c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

4. Compound heterozygous c-Mpl mutations in a child with congenital amegakaryocytic thrombocytopenia: Functional characterization and a review of the literature

5. Identification of MPL R102P Mutation in Hereditary Thrombocytosis

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP