Výsledky vyhledávání - "Mark G. Olavesen"

A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome

Autor: Rosemarie Davidson, Richard J. Stephens, Angela F. Davies, Iman Abusaad, Mark G. Olavesen, Nicole Van Regemorter, Jiannis Ragoussis, Frances Flinter, Daniele Delneste, E. Vamos

Publikováno v: Human Genetics. 98:454-459

Deletions of the short arm of chromosome 6 are relatively rare, only 16 cases having been described in the literature so far. Here we present a detailed investigation by fluorescence in situ hybridisation of two further cases with different but overl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dec99bbcc606f121eca4acc9813f2f9
https://doi.org/10.1007/s004390050239

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UP-REGULATION OF TYPE 1 PLASMINOGEN ACTIVATOR INHIBITOR MESSENGER RNA WITH THROMBOTIC CHANGES IN RENAL GRAFTS1

Autor: Frederick W. K. Tam, Mark G. Olavesen, Judith A. Wolff, Julian R. Pratt, Yiming Wang, Steven H. Sacks, Barrie Hartley

Publikováno v: Transplantation. 61:684-689

Small vessel thrombosis is a prominent feature in kidneys undergoing vascular rejection. Type I and type 2 plasminogen activator inhibitors (PAI-1 and PAI-2, respectively) are known to mediate thrombosis. To examine the potential role of PAI-1 and PA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e081123ea44f5152a3d4a9c29470763d
https://doi.org/10.1097/00007890-199603150-00002

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Localization of a new gene adjacent to the HSP70 genes in human and mouse MHCs

Autor: R.D. Campbell, Margriet Snoek, Mark G. Olavesen

Publikováno v: Immunogenetics. 37:394-396

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d6f77695f7ace26b7b3ffb664e8a91e
https://doi.org/10.1007/bf00216806

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Localization of eight additional genes in the human major histocompatibility complex, including the gene encoding the casein kinase II beta subunit (CSNK2B)

Autor: Jones H, Campbell Rd, Wendy Thomson, Albertella Mr, Mark G. Olavesen

Publikováno v: Genomics. 36(2)

A wide range of autoimmune and other diseases are known to be associated with the major histocompatibility complex. Many of these diseases are linked to the genes encoding the polymorphic histocompatibility antigens in the class I and class II region

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27dd2d5796b3759a4724642cc981349f
https://pubmed.ncbi.nlm.nih.gov/8812450

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