Factor XIII 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
A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection.
Casanova Jean-Laurent, Su Helen C
Cell Vol 181(6)
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Date 11 Jun 2020
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
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
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
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
Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
Gacy A M, Goellner G, Juranić N, Macura S, McMurray C T
Cell Vol 81(4)
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Date 19 May 1995
Research
Structures of DPAGT1 Explain Glycosylation Disease Mechanisms and Advance TB Antibiotic Design.
Dong Yin Yao, Wang Hua, Pike Ashley C W, Cochrane Stephen A, Hamedzadeh Sadra ...
Cell Vol 175(4)
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Date 01 Nov 2018
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
Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor.
Lebrón J A, Bennett M J, Vaughn D E, Chirino A J, Snow P M ...
Cell Vol 93(1)
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Date 03 Apr 1998
Research
Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease.
Vassar R, Coulombe P A, Degenstein L, Albers K, Fuchs E
Cell Vol 64(2)
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Date 25 Jan 1991
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