Výsledky vyhledávání - "Aylin Kirchner"

Akademický článek

Clinical and functional implications of microRNA mutations in a cohort of 935 patients with myelodysplastic syndromes and acute myeloid leukemia

Publikováno v: Haematologica, Vol 100, Iss 4 (2015)

Externí odkaz: https://doaj.org/article/6bc7f35c6b2348ec9d7dc6a1c9bd95b9

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Akademický článek

Genetic characterization of acquired aplastic anemia by targeted sequencing

Autor: Michael Heuser, Carola Schlarmann, Vera Dobbernack, Victoria Panagiota, Lutz Wiehlmann, Carolin Walter, Fabian Beier, Patrick Ziegler, Haiyang Yun, Sofia Kade, Aylin Kirchner, Liu Huang, Christian Koenecke, Matthias Eder, Tim H. Brümmendorf, Martin Dugas, Arnold Ganser, Felicitas Thol

Publikováno v: Haematologica, Vol 99, Iss 9 (2014)

Externí odkaz: https://doaj.org/article/e99cde6ff38d40f5bdf8aad0155716a5

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Clinical and functional implications of microRNA mutations in a cohort of 935 patients with myelodysplastic syndromes and acute myeloid leukemia

Publikováno v: Haematologica. 100:e122-e124

MicroRNAs are short (20–40 nucleotides) non-coding RNA molecules that are responsible for the post-transcriptional regulation of gene expression. Aberrant expression of microRNAs has been associated with various malignancies.[1][1],[2][2] Specifica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bcc07405e91f50f3cc699615cde355d
https://doi.org/10.3324/haematol.2014.120345

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Genetic characterization of acquired aplastic anemia by targeted sequencing

Autor: Vera Dobbernack, Arnold Ganser, Martin Dugas, Christian Koenecke, Lutz Wiehlmann, Patrick Ziegler, Tim H. Brümmendorf, Carolin Walter, Liu Huang, Aylin Kirchner, Haiyang Yun, Felicitas Thol, Victoria Panagiota, Matthias Eder, Fabian Beier, Sofia Kade, Michael Heuser, Carola Schlarmann

Publikováno v: Haematologica. 99:e165-e167

Aplastic anemia (AA) is a rare but life-threatening bone marrow failure syndrome; diagnosis is based on cytopenias in peripheral blood and hypocellularity in bone marrow. The distinction between AA and hypocellular myelodysplastic syndrome (MDS) is o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c3167e8e27a1b9b0b85872177cf743a
https://doi.org/10.3324/haematol.2013.101642

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Mutations in the cohesin complex in acute myeloid leukemia: clinical and prognostic implications

Publikováno v: Blood. 123(6)

Mutations in the cohesin complex are novel, genetic lesions in acute myeloid leukemia (AML) that are not well characterized. In this study, we analyzed the frequency, clinical, and prognostic implications of mutations in STAG1, STAG2, SMC1A, SMC3, an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39ec0b5fdf94578725a7d83c5b4467e
https://pubmed.ncbi.nlm.nih.gov/24335498

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The Clinical and Prognostic Influence Of Mutations In The Cohesin Complex In Acute Myeloid Leukemia

Publikováno v: Blood. 122:1314-1314

Background The cohesin complex presents a ring structure that regulates chromosome segregation during meiosis and mitosis and is thus essential for cell division. Genes that belong to the cohesin complex in somatic vertebrate cells are SMC1A, SMC3, R

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8f190d503febecf687e236d58e7c7650
https://doi.org/10.1182/blood.v122.21.1314.1314

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Genetic Characterization Of Aplastic Anemia Patients By Targeted Sequencing

Autor: Tim H. Brümmendorf, Vera Dobbernack, Arnold Ganser, Aylin Kirchner, Matthias Eder, V Panagiota, Patrick Ziegler, Liu Huang, Haiyang Yun, Lutz Wiehlmann, Fabian Beier, Carolin Walter, Sofia Kade, Felicitas Thol, Christian Koenecke, Martin Dugas, Michael Heuser, Carola Schlarmann

Publikováno v: ResearcherID

Introduction Aplastic anemia (AA) is a rare but life-threatening bone marrow failure syndrome, which is diagnosed based on cytopenias in peripheral blood and hypocellularity in the bone marrow. The distinction between AA and hypocellular myelodysplas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66b7cf9f99616531a8bc433730489eb
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000331385005215&KeyUID=WOS:000331385005215

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Analysis Of Micro-RNA-142 Mutations In a Cohort Of 944 Patients With MDS and AML

Autor: Juergen Krauter, Michael Stadler, Christian Koenecke, Arnold Ganser, Thomas Schroeder, Felicitas Thol, Michael Heuser, Uwe Platzbecker, Aylin Kirchner, Christian Thiede, Guido Kobbe, Oliver G. Ottmann, Sofia Kade, Gesine Bug, Wolf-Karsten Hofmann, Nicolaus Kröger, Rabia Shahswar

Publikováno v: ResearcherID

Background MicroRNAs are short (20-40 nucleotides) non-coding RNA molecules that are responsible for the post-transcriptional regulation of gene expression. Aberrant expression of MicroRNAs has been associated with various malignancies. Specifically,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc5a8abddfc2113ec08ae0dc8996a42e
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000331385006076&KeyUID=WOS:000331385006076

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