Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Johnson M Liu"'
Autor:
Sharon A Singh, Tracie A Goldberg, Adrianna L Henson, Sehba Husain-Krautter, Abdallah Nihrane, Lionel Blanc, Steven R Ellis, Jeffrey M Lipton, Johnson M Liu
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e89098 (2014)
Diamond Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome caused by ribosomal protein haploinsufficiency. DBA exhibits marked phenotypic variability, commonly presenting with erythroid hypoplasia, less consistently with non-eryth
Externí odkaz:
https://doaj.org/article/e7e05754df2d4038a1531abf0ed91625
Publikováno v:
Semin Hematol
Fanconi anemia, telomeropathies and ribosomopathies are members of the inherited bone marrow failure syndromes, rare genetic disorders that lead to failure of hematopoiesis, developmental abnormalities, and cancer predisposition. While each disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a84e50bf59a3f97ee3a7cea16828c1
https://doi.org/10.1053/j.seminhematol.2022.01.003
https://doi.org/10.1053/j.seminhematol.2022.01.003
Publikováno v:
Exp Biol Med (Maywood)
COVID-19 or SARS-CoV-2 infection can lead to severe acute respiratory distress syndrome/pneumonia with features of cytokine storm reminiscent of secondary hemophagocytic lymphohistiocytosis (HLH), which can be diagnosed by the calculated HScore. Rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c082d40c2853bb0fc5e73ef4264cdaaf
https://doi.org/10.1177/1535370220962043
https://doi.org/10.1177/1535370220962043
Autor:
Johnson M Liu, Jeffrey Chi
Publikováno v:
Exp Biol Med (Maywood)
Cytokine storm is an umbrella term that describes an inflammatory syndrome characterized by elevated levels of circulating cytokines and hyperactivation of innate and/or adaptive immune cells. One type of cytokine storm is hemophagocytic lymphohistio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4b77f4d9e27223e694e08d9cc7f01c4
https://pubmed.ncbi.nlm.nih.gov/35068219
https://pubmed.ncbi.nlm.nih.gov/35068219
Publikováno v:
Haematologica, Vol 95, Iss 1 (2010)
Background Diamond-Blackfan anemia and Shwachman-Diamond syndrome are inherited bone marrow failure syndromes linked to defects in ribosome synthesis. The purpose of this study was to determine whether yeast models for Diamond-Blackfan anemia and Shw
Externí odkaz:
https://doaj.org/article/98e205b2e8d34055806baeb27aeb8e0b
Publikováno v:
BMJ case reports. 2018
A 67-year-old right-handed woman presented with dysarthria, left upper extremity weakness and right-sided neglect of 3 hours duration. Imaging of the brain revealed acute right middle cerebral artery stroke; however, tissue plasminogen activator coul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17ba98df7649a714f86d0376671540e2
https://pubmed.ncbi.nlm.nih.gov/29437728
https://pubmed.ncbi.nlm.nih.gov/29437728
Publikováno v:
Leukemia Research Reports
Leukemia Research Reports, Vol 4, Iss 1, Pp 36-38 (2015)
Leukemia Research Reports, Vol 4, Iss 1, Pp 36-38 (2015)
Pregnancy in women with paroxysmal nocturnal hemoglobinuria (PNH) is associated with increased maternal and fetal morbidity and mortality. There is limited published experience regarding therapy of PNH during pregnancy. We describe a case of a 30 yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca6c8f0c02aec7088db099057b0591d2
http://europepmc.org/articles/PMC4454784
http://europepmc.org/articles/PMC4454784
Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q− syndrome
Autor:
Eva Atsidaftos, Michael Landowski, Anupama Narla, Johnson M. Liu, Robert J. Arceci, Jeffrey M. Lipton, Thomas C. Markello, Sharon A. Singh, Adrianna Vlachos, Ellen Muir, Steven R. Ellis, Hanna T. Gazda, Lionel Blanc, David M. Bodine, Jason E. Farrar, Benjamin L. Ebert
Publikováno v:
Blood. 122:2487-2490
Classical 5q- syndrome is an acquired macrocytic anemia of the elderly. Similar to Diamond Blackfan anemia (DBA), an inherited red cell aplasia, the bone marrow is characterized by a paucity of erythroid precursors. RPS14 deletions in combination wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b44f943b6bba120bed2b47692d36b7
https://doi.org/10.1182/blood-2013-06-509935
https://doi.org/10.1182/blood-2013-06-509935
Autor:
Johnson M. Liu, Demet Gokalp-Yasar
Publikováno v:
International Blood Research & Reviews. 1:14-21
Whereas deletions involving the long arm of chromosome 5 are among the most common chromosomal abnormalities in myelodysplastic syndrome (MDS), isolated del(5q) MDS, which includes the 5q- syndrome, is rare and characterized by hypoplastic anemia and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc645edec441be61f00fd22a95f85d80
https://doi.org/10.9734/ibrr/2013/3234
https://doi.org/10.9734/ibrr/2013/3234
Autor:
Johnson M. Liu, Diane L D'Allard
Publikováno v:
Human gene therapy. 27(10)
Diamond blackfan anemia (DBA) is a well-known inherited bone marrow failure syndrome mostly caused by mutations in ribosomal protein (RP) genes but also rarely in the hematopoietic transcription factor gene, GATA1, or TSR2, a ribosomal protein (Rps26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73263b3c5a4c27efa933c8b53575626
https://pubmed.ncbi.nlm.nih.gov/27550323
https://pubmed.ncbi.nlm.nih.gov/27550323