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Items: 4

1.
Prenatal diagnosis of a 5q35.3 microduplication involving part of the ADAMTS2 locus: a likely benign variant without apparent phenotypic abnormality: Case series
Fagui Yue, Yang Yu, Qi Xi, Hongguo Zhang, Yuting Jiang, Shibo Li, Ruizhi Liu, Ruixue Wang
Medicine (Baltimore) 2019 Dec; 98(49): e18258. Published online 2019 Dec 10. doi: 10.1097/MD.0000000000018258
PMCID:
PMC6919437
AbstractArticlePDF–341K
2.
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.
A Colige, A L Sieron, S W Li, U Schwarze, E Petty, W Wertelecki, W Wilcox, D Krakow, D H Cohn, W Reardon, P H Byers, C M Lapière, D J Prockop, B V Nusgens
Am J Hum Genet. 1999 Aug; 65(2): 308–317. doi: 10.1086/302504
PMCID:
PMC1377929
SummaryPDF–450K
3.
DNA methylation data for identification of epigenetic targets of resveratrol in triple negative breast cancer cells
Rubiceli Medina-Aguilar, Carlos Pérez-Plasencia, Patricio Gariglio, Laurence A. Marchat, Ali Flores-Pérez, César López-Camarillo, Jaime García Mena
Data Brief. 2017 Apr; 11: 169–182. Published online 2017 Feb 9. doi: 10.1016/j.dib.2017.02.006
PMCID:
PMC5312642
AbstractArticlePDF–431K
4.
Chondrogenic differentiation potential of osteoarthritic chondrocytes and their possible use in matrix-associated autologous chondrocyte transplantation
Tilo Dehne, Camilla Karlsson, Jochen Ringe, Michael Sittinger, Anders Lindahl
Arthritis Res Ther. 2009; 11(5): R133. Published online 2009 Sep 2. doi: 10.1186/ar2800
PMCID:
PMC2787268
AbstractArticlePDF–3.4M

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