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- Bookeditor, Alexander Birbrair.Summary: This volume explores pericytes' roles under distinct pathological conditions, ranging from tumors, ALS, Alzheimers disease, Multiple Sclerosis, stroke, diabetes, atherosclerosis, muscular dystrophies and more. Together with its companion volumes Pericyte Biology in Different Organs and Pericyte Biology – Novel Concepts, Pericyte Biology in Disease presents a comprehensive update on the latest information and most novel functions attributed to pericytes. To those researchers newer to this area, it will be useful to have the background information on these cells' unique history. It will be invaluable for both advanced cell biology students as well as researchers in cell biology, stem cell biology and clinicians involved with these specific diseases.
Contents:
Pericytes in cutaneous wound healing
Pericytes in glioblastomas: multifaceted role within tumor microenvironments and potential for therapeutic interventions
Pericytes in breast cancer
Pericytes in sarcomas and other mesenchymal tumors
Pericytes in metastasis
The role of pericytes in Amyotrophic Lateral Sclerosis
Pericytes in Alzheimers Disease: novel clues to cerebral amyloid angiopathy pathogenesis
Pericytes in Multiple Sclerosis
Pericytes in ischemic stroke
Pericytes in Hereditary Hemorrhagic Telangiectasia
Pericytes in primary familial brain calcification
Pericytes in type 2 diabetes
Pericytes in atherosclerosis
Pericytes in chronic lung disease
Pericytes in muscular dystrophies
Index. - ArticleHumphries P, Old R, Coggins LW, McShane T, Watson C, Paul J.Nucleic Acids Res. 1978 Mar;5(3):905-24.Details are presented of the in vitro synthesis of double-stranded DNA complementary to purified Xenopus globin messenger RNA, using a combination of reverse transcriptase, fragment 'A' of E. coli DNA polymerase 1 and S1 endonuclease. After selection of duplex DNA molecules approaching the length of Xenopus globin messenger RNA by sedimentation of the DNA through neutral sucrose gradients, the 3'-OH termini of the synthetic globin gene sequences were extended with short tracts of oligo dGMP using terminal transferase. This material was integrated into oligo dCMP-extended linear pCR1 plasmid DNA and amplified by transfection of E. coli. Plasmids carrying globin sequences were identified by hybridization of 32P-labelled globin mRNA to total cellular DNA in situ, by hybridization of purified plasmids to globin cDNA in solution, by analysis of recombinant DNA on polyacrylamide and agarose gels, and by heteroduplex mapping. The results show that extensive DNA copies of Xenopus globin mRNA have been integrated into recombinant plasmids.