Access the latest scientific research and medical evidence related to Blood Coagulation Disorders, Inherited 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 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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8406 Abstracts
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
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
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
Disease-specific induced pluripotent stem cells.
Park In-Hyun, Arora Natasha, Huo Hongguang, Maherali Nimet, Ahfeldt Tim ...
Cell Vol 134(5)
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Date 05 Sep 2008
Research
Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay.
Tewhey Ryan, Kotliar Dylan, Park Daniel S, Liu Brandon, Winnicki Sarah ...
Cell Vol 165(6)
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Date 02 Jun 2016
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
Genomic instability and aging-like phenotype in the absence of mammalian SIRT6.
Mostoslavsky Raul, Chua Katrin F, Lombard David B, Pang Wendy W, Fischer Miriam R ...
Cell Vol 124(2)
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Date 27 Jan 2006
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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Date 23 Apr 2015
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