Literature DB >> 28663223

Singling out FLI1 in Paris-Trousseau syndrome.

Hervé Falet1.   

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Year:  2017        PMID: 28663223      PMCID: PMC5492094          DOI: 10.1182/blood-2017-05-781252

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


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  10 in total

1.  Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1.

Authors:  William S Stevenson; David J Rabbolini; Lucinda Beutler; Qiang Chen; Sara Gabrielli; Joel P Mackay; Timothy A Brighton; Christopher M Ward; Marie-Christine Morel-Kopp
Journal:  Blood       Date:  2015-08-27       Impact factor: 22.113

2.  Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia.

Authors:  A Hart; F Melet; P Grossfeld; K Chien; C Jones; A Tunnacliffe; R Favier; A Bernstein
Journal:  Immunity       Date:  2000-08       Impact factor: 31.745

3.  Defective megakaryopoiesis and abnormal erythroid development in Fli-1 gene-targeted mice.

Authors:  Hiroshi Kawada; Tatsuya Ito; Pamela N Pharr; Demetri D Spyropoulos; Dennis K Watson; Makio Ogawa
Journal:  Int J Hematol       Date:  2001-06       Impact factor: 2.490

Review 4.  Hematopoietic transcription factor mutations: important players in inherited platelet defects.

Authors:  Natthapol Songdej; A Koneti Rao
Journal:  Blood       Date:  2017-04-17       Impact factor: 22.113

5.  Paris-Trousseau syndrome : clinical, hematological, molecular data of ten new cases.

Authors:  Remi Favier; Katayoun Jondeau; Patrice Boutard; Paul Grossfeld; Philippe Reinert; Christopher Jones; Francesco Bertoni; Elisabeth M Cramer
Journal:  Thromb Haemost       Date:  2003-11       Impact factor: 5.249

6.  FLI1 level during megakaryopoiesis affects thrombopoiesis and platelet biology.

Authors:  Karen K Vo; Danuta J Jarocha; Randolph B Lyde; Vincent Hayes; Christopher S Thom; Spencer K Sullivan; Deborah L French; Mortimer Poncz
Journal:  Blood       Date:  2017-04-21       Impact factor: 22.113

7.  A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23.

Authors:  J Breton-Gorius; R Favier; J Guichard; D Cherif; R Berger; N Debili; W Vainchenker; L Douay
Journal:  Blood       Date:  1995-04-01       Impact factor: 22.113

8.  FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.

Authors:  Hana Raslova; Emiko Komura; Jean Pierre Le Couédic; Frederic Larbret; Najet Debili; Jean Feunteun; Olivier Danos; Olivier Albagli; William Vainchenker; Rémi Favier
Journal:  J Clin Invest       Date:  2004-07       Impact factor: 14.808

9.  Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.

Authors:  Jacqueline Stockley; Neil V Morgan; Danai Bem; Gillian C Lowe; Marie Lordkipanidzé; Ban Dawood; Michael A Simpson; Kirsty Macfarlane; Kevin Horner; Vincenzo C Leo; Katherine Talks; Jayashree Motwani; Jonathan T Wilde; Peter W Collins; Michael Makris; Steve P Watson; Martina E Daly
Journal:  Blood       Date:  2013-10-07       Impact factor: 22.113

10.  Genome-wide analysis of simultaneous GATA1/2, RUNX1, FLI1, and SCL binding in megakaryocytes identifies hematopoietic regulators.

Authors:  Marloes R Tijssen; Ana Cvejic; Anagha Joshi; Rebecca L Hannah; Rita Ferreira; Ariel Forrai; Dana C Bellissimo; S Helen Oram; Peter A Smethurst; Nicola K Wilson; Xiaonan Wang; Katrin Ottersbach; Derek L Stemple; Anthony R Green; Willem H Ouwehand; Berthold Göttgens
Journal:  Dev Cell       Date:  2011-05-17       Impact factor: 12.270

  10 in total

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