Access the latest scientific research and medical evidence related to Platelet Storage Pool Deficiency treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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6574 Abstracts
Research
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Khajuria Rajiv K, Munschauer Mathias, Ulirsch Jacob C, Fiorini Claudia, Ludwig Leif S ...
Cell Vol 173(1)
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Date 22 Mar 2018
Research
Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice.
Ueki Yasuyoshi, Lin Chin-Yu, Senoo Makoto, Ebihara Takeshi, Agata Naoki ...
Cell Vol 128(1)
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Date 12 Jan 2007
Research
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
Ho M, Chelly J, Carter N, Danek A, Crocker P ...
Cell Vol 77(6)
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Date 17 Jun 1994
Research
Loss of fibrinogen rescues mice from the pleiotropic effects of plasminogen deficiency.
Bugge T H, Kombrinck K W, Flick M J, Daugherty C C, Danton M J ...
Cell Vol 87(4)
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Date 15 Nov 1996
Research
Inducible secretion of large, biologically potent von Willebrand factor multimers.
Sporn L A, Marder V J, Wagner D D
Cell Vol 46(2)
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Date 18 Jul 1986
Research
Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII.
Nichols W C, Seligsohn U, Zivelin A, Terry V H, Hertel C E ...
Cell Vol 93(1)
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Date 03 Apr 1998
Research
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene.
White R A, Peters L L, Adkison L R, Korsgren C, Cohen C M ...
Nature genetics Vol 2(1)
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Date 01 Sep 1992
Research
Physiogenomic resources for rat models of heart, lung and blood disorders.
Malek Renae L, Wang Hong-ying, Kwitek Anne E, Greene Andrew S, Bhagabati Nirmal ...
Nature genetics Vol 38(2)
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Date 01 Feb 2006
Research
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Iotchkova Valentina, Huang Jie, Morris John A, Jain Deepti, Barbieri Caterina ...
Nature genetics Vol 48(11)
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Date 01 Nov 2016
Research
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.
Noetzli Leila, Lo Richard W, Lee-Sherick Alisa B, Callaghan Michael, Noris Patrizia ...
Nature genetics Vol 47(5)
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Date 01 May 2015
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