Developmental Stage-Specific Manifestations of Absent TPO/c-MPL Signalling in Newborn Mice.

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Developmental Stage-Specific Manifestations of Absent TPO/c-MPL Signalling in Newborn Mice.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

@en

Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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P1476

Developmental Stage-Specific M ...... PL Signalling in Newborn Mice.

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P2093

Donald Mager

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Francisca Ferrer-Marin

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Joseph Italiano

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Karin Hoffmeister

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Martha Sola-Visner

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Sihem Bihorel

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Viola Lorenz

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William B Slayton

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Zhi-Jian Liu

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Zhongbo Hu

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P2860

Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia

c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome.

Thrombocytopenia with absent radii: frequency of marrow megakaryocyte progenitors, proliferative characteristics, and megakaryocyte growth and development factor responsiveness.

Dose-response relationship of megakaryocyte progenitors from the bone marrow of thrombocytopenic and non-thrombocytopenic neonates to recombinant thrombopoietin.

Thrombocytopenia with absent radii (TAR syndrome): new advances in the mechanism of thrombocytopenia.

Absence of GPIbalpha is responsible for aberrant membrane development during megakaryocyte maturation: ultrastructural study using a transgenic model.

Congenital amegakaryocytic thrombocytopenia: a retrospective clinical analysis of 20 patients.

MPL mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the disease.

A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopenia.

P304

2322-2333

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P31

scholarly article

P356

10.1160/TH17-06-0433

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P433

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P478

117

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P50

Benjamin T. Kile

Haley Elizabeth Ramsey

P577

2017-12-06T00:00:00Z

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P698

29212120

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P932

5911346

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