Panniculitis, Nodular Nonsuppurative 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
Engineering Phage Host-Range and Suppressing Bacterial Resistance through Phage Tail Fiber Mutagenesis.
Yehl Kevin, Lemire Sébastien, Yang Andrew C, Ando Hiroki, Mimee Mark ...
Cell Vol 179(2)
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Date 03 Oct 2019
Research
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover.
Holmbeck K, Bianco P, Caterina J, Yamada S, Kromer M ...
Cell Vol 99(1)
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Date 01 Oct 1999
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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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Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders...
Downing A K, Knott V, Werner J M, Cardy C M, Campbell I D ...
Cell Vol 85(4)
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Date 17 May 1996
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CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Morello Roy, Bertin Terry K, Chen Yuqing, Hicks John, Tonachini Laura ...
Cell Vol 127(2)
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Date 20 Oct 2006
Research
A human autoimmune protein associated with U1 RNA contains a region of homology that is cross-reactive with retroviral p30gag antigen.
Query C C, Keene J D
Cell Vol 51(2)
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Date 23 Oct 1987
Research
Hepatic acetyl CoA links adipose tissue inflammation to hepatic insulin resistance and type 2 diabetes.
Perry Rachel J, Camporez João-Paulo G, Kursawe Romy, Titchenell Paul M, Zhang Dongyan ...
Cell Vol 160(4)
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Date 12 Feb 2015
Research
Small nuclear ribonucleoprotein particle assembly in vivo: demonstration of a 6S RNA-free core precursor and posttranslational modification.
Fisher D E, Conner G E, Reeves W H, Wisniewolski R, Blobel G
Cell Vol 42(3)
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Date 01 Oct 1985
Research
The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.
Cheng J, Syder A J, Yu Q C, Letai A, Paller A S ...
Cell Vol 70(5)
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Date 04 Sep 1992
Research
Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation.
Mann G B, Fowler K J, Gabriel A, Nice E C, Williams R L ...
Cell Vol 73(2)
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Date 23 Apr 1993
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