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Dagmar Pospisilova

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Physiology

Chemicals & Drugs

Anatomy

Living Beings

Procedures

DNA Mutational Analysis

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Publications

TOP 3
Cmejla Radek; Cmejlova Jana; Handrkova Helena; Petrak Jiri; Petrtylova Kvetoslava; Mihal Vladimir; Stary Jan; Cerna Zdena; Jabali Yahia; Pospisilova Dagmar
Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia.
Cario Holger; Schwarz Klaus; Herter Jan M; Komrska Vladimir; McMullin Mary F; Minkov Milen; Niemeyer Charlotte; Pospisilova Dagmar; Reinhard Harald; Debatin Klaus-Michael; Pahl Heike L
Clinical and molecular characterisation of a prospectively collected cohort of children and adolescents with polycythemia vera.
Veselovska Jitka; Pospisilova Dagmar; Pekova Sona; Horvathova Monika; Solna Renata; Cmejlova Jana; Cmejla Radek; Belickova Monika; Mihal Vladimir; Stary Jan; Divoky Vladimir
Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.

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All Publications

2009: Cmejla Radek; Cmejlova Jana; Handrkova Helena; Petrak Jiri; Petrtylova Kvetoslava; Mihal Vladimir; Stary Jan; Cerna Zdena; Jabali Yahia; Pospisilova Dagmar
Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia.
Human mutation 2009;30(3):321-7.
2008: Cario Holger; Schwarz Klaus; Herter Jan M; Komrska Vladimir; McMullin Mary F; Minkov Milen; Niemeyer Charlotte; Pospisilova Dagmar; Reinhard Harald; Debatin Klaus-Michael; Pahl Heike L
Clinical and molecular characterisation of a prospectively collected cohort of children and adolescents with polycythemia vera.
British journal of haematology 2008;142(4):622-6.
2008: Veselovska Jitka; Pospisilova Dagmar; Pekova Sona; Horvathova Monika; Solna Renata; Cmejlova Jana; Cmejla Radek; Belickova Monika; Mihal Vladimir; Stary Jan; Divoky Vladimir
Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.
Leukemia research 2008;32(3):369-77.
2007: Cmejla Radek; Cmejlova Jana; Handrkova Helena; Petrak Jiri; Pospisilova Dagmar
Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia.
Human mutation 2007;28(12):1178-82.
2007: Pospisilova D; Cmejlova J; Hak J; Adam T; Cmejla R
Successful treatment of a Diamond-Blackfan anemia patient with amino acid leucine.
Haematologica 2007;92(5):e66-7.
2007: Jelinek Jaroslav; Issa Jean-Pierre J; He Rong; Cmejla Radek; Cmejlova Jana; Pospisilova Dagmar
RPS19 and JAK2 genes are not silenced by DNA methylation in diamond blackfan anemia.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2007;29(3):207-8.
2006: Cmejlova Jana; Dolezalova Ludmila; Pospisilova Dagmar; Petrtylova Kvetoslava; Petrak Jiri; Cmejla Radek
Translational efficiency in patients with Diamond-Blackfan anemia.
Haematologica 2006;91(11):1456-64.
2006: Pospisilova Dagmar; Mims Martha P; Nemeth Elizabeta; Ganz Tomas; Prchal Josef T
DMT1 mutation: response of anemia to darbepoetin administration and implications for iron homeostasis.
Blood 2006;108(1):404-5.
2006: Cmejlova Jana; Cerna Zdena; Votava Tomas; Pospisilova Dagmar; Cmejla Radek
Identification of a new in-frame deletion of six amino acids in ribosomal protein S19 in a patient with Diamond-Blackfan anemia.
Blood cells, molecules & diseases 2006;36(3):337-41.
2005: Priwitzerova Monika; Nie Guangjun; Sheftel Alex D; Pospisilova Dagmar; Divoky Vladimir; Ponka Prem
Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake.
Blood 2005;106(12):3985-7.
2005: Mims Martha P; Guan Yongli; Pospisilova Dagmar; Priwitzerova Monika; Indrak Karel; Ponka Prem; Divoky Vladimir; Prchal Josef T
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.
Blood 2005;105(3):1337-42.
2004: Pospisilova Dagmar; Cmejlova Jana; Slavik Ludek; Cmejla Radek
Elevated thrombopoietin levels and alterations in the sequence of its receptor, c-Mpl, in patients with Diamond-Blackfan anemia.
Haematologica 2004;89(11):1391-2.
2004: Priwitzerova Monika; Pospisilova Dagmar; Prchal Josef T; Indrak Karel; Hlobilkova Alice; Mihal Vladimir; Ponka Prem; Divoky Vladimir
Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells.
Blood 2004;103(10):3991-2.
2004: Mihal Vladimir; Hajduch Marian; Noskova Vera; Janostakova Anna; Safarova Maria; Orel Miroslav; Kouzmina Galina; Stary Jan; Blazek Bohuslav; Pospisilova Dagmar
The analysis of correlations between drug resistance and clinical/laboratory measures found in a group of children with all treated by ALL-BFM 90 protocol.
Bulletin du cancer 2004;91(4):E80-9.
2003: Zivny Jan; Jelinek Jaroslav; Pospisilova Dagmar; Plasilova Magdalena; Necas Emanuel; Stopka Tomas
Diamond blackfan anemia stem cells fail to repopulate erythropoiesis in NOD/SCID mice.
Blood cells, molecules & diseases 2003;31(1):93-7.
2002: Cmejlova Jana; Pospisilova Dagmar; Cmejla Radek
Transcription factor GATA-4 is not involved in Diamond-Blackfan anaemia.
Haematologica 2002;87(7):ELT30.
2001: Cmejla R; Blafkova J; Stopka T; Jelinek J; Petrtylova K; Pospisilova D
Ribosomal proteins S3a, S13, S16, and S24 are not mutated in patients with Diamond-Blackfan anemia.
Blood 2001;97(2):579-80.
2000: Cmejla R; Blafkova J; Stopka T; Zavadil J; Pospisilova D; Mihal V; Petrtylova K; Jelinek J
Ribosomal protein S19 gene mutations in patients with diamond-blackfan anemia and identification of ribosomal protein S19 pseudogenes.
Blood cells, molecules & diseases 2000;26(2):124-32.

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Dagmar Pospisilova

Research Profile (preview)

Disorders

Physiology

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Network (preview)

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