Protein S Deficiency research, articles, guidelines & medical evidence database search.
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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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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
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
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
Guernsey Duane L, Jiang Haiyan, Campagna Dean R, Evans Susan C, Ferguson Meghan ...
Nature genetics Vol 41(6)
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Date 01 Jun 2009
Research
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Kamatani Yoichiro, Matsuda Koichi, Okada Yukinori, Kubo Michiaki, Hosono Naoya ...
Nature genetics Vol 42(3)
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Date 01 Mar 2010
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