Supplementary Figure 3 from Accumulation of Multipotent Progenitors with a Basal Differentiation Bias during Aging of Human Mammary Epithelia

Autor: Mark A. LaBarge, Martha R. Stampfer, Alexander D. Borowsky, Ole W. Petersen, Morag Park, Rene Villadsen, Diana E. Guo, Agla J. Fridriksdottir, Klara Sputova, Fanny A. Pelissier, Francois Pepin, James C. Garbe

PDF file - 2.3MB, Lineage marker distributions in cultured and uncultured HMEC. Sevenparameter flow cytometry analyses of 4th passage HMEC strains

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66741ffade0f5d0bd48514624f9d479c
https://doi.org/10.1158/0008-5472.22393472.v1

Supplementary Figure 1 from Accumulation of Multipotent Progenitors with a Basal Differentiation Bias during Aging of Human Mammary Epithelia

Autor: Mark A. LaBarge, Martha R. Stampfer, Alexander D. Borowsky, Ole W. Petersen, Morag Park, Rene Villadsen, Diana E. Guo, Agla J. Fridriksdottir, Klara Sputova, Fanny A. Pelissier, Francois Pepin, James C. Garbe

PDF file - 326K, Cultured pre-stasis finite lifespan HMEC at early passage preserve key features of HMEC in vivo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8013b8f4fd81355d5137438e2f9e83ee
https://doi.org/10.1158/0008-5472.22393478

A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.

Autor: Nasrine Bendjilali, Helen Kim, Shantel Weinsheimer, Diana E Guo, Pui-Yan Kwok, Jonathan G Zaroff, Stephen Sidney, Michael T Lawton, Charles E McCulloch, Bobby P C Koeleman, Catharina J M Klijn, William L Young, Ludmila Pawlikowska

Publikováno v: PLoS ONE, Vol 8, Iss 10, p e71434 (2013)

Brain arteriovenous malformations (BAVM) are clusters of abnormal blood vessels, with shunting of blood from the arterial to venous circulation and a high risk of rupture and intracranial hemorrhage. Most BAVMs are sporadic, but also occur in patient

Externí odkaz: https://doaj.org/article/04907797385149b98403c9bdddf9e49e

Abstract WP427: Health-related Quality of Life Measures in Familial Cerebral Cavernous Malformation Patients

Autor: Kimberly Yan, Diana E. Guo, Amy Akers, Mary Harrigan, Keva C DeKay, Jeffrey Nelson, Leslie Morrison, Mary R. Bartlett, Blaine L. Hart, Yashar Kalani, Joseph M. Zabramski, Charles E. McCulloch, Helen Kim

Publikováno v: Stroke. 49

Background: Patient-reported quality of life (QoL) using standardized tools have been proposed as outcome measures in clinical trials. The NeuroQoL scale has been evaluated in patients with common neurological disorders (e.g., ischemic stroke, epilep

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ddc04763e9dec92f2827ecfd50b38f1d
https://doi.org/10.1161/str.49.suppl_1.wp427

Genome-wide association study of sporadic brain arteriovenous malformations

Autor: Charles E. McCulloch, Alfredo Puca, Shantel Weinsheimer, Nasrine Bendjilali, Ludmila Pawlikowska, Roberto Pola, Matthias Simon, Rustam Al-Shahi Salman, Jonathan G. Zaroff, J. Nelson, Catharina J.M. Klijn, Bobby P. C Koeleman, Helen Kim, Azize Bostroem, William L. Young, Carmelo Lucio Sturiale, Stephen Sidney, Diana E. Guo, Marco Maria Fontanella, Michael T. Lawton, Jonathan Berg

Publikováno v: Journal of Neurology, Neurosurgery, and Psychiatry, 87, 916-23
Weinsheimer, S, Bendjilali, N, Nelson, J, Guo, D E, Zaroff, J G, Sidney, S, McCulloch, C E, Al-Shahi Salman, R, Berg, J N, Koeleman, B P C, Simon, M, Bostroem, A, Fontanella, M, Sturiale, C L, Pola, R, Puca, A, Lawton, M T, Young, W L, Pawlikowska, L, Klijn, C J M, Kim, H 2016, ' Genome-wide association study of sporadic brain arteriovenous malformations ', Journal of Neurology, Neurosurgery & Psychiatry . https://doi.org/10.1136/jnnp-2015-312272
Journal of Neurology, Neurosurgery, and Psychiatry, 87, 9, pp. 916-23
Journal of Neurology, Neurosurgery and Psychiatry, 87(9), 916. BMJ Publishing Group
Journal of neurology, neurosurgery, and psychiatry, vol 87, iss 9

BACKGROUND: The pathogenesis of sporadic brain arteriovenous malformations (BAVMs) remains unknown, but studies suggest a genetic component. We estimated the heritability of sporadic BAVM and performed a genome-wide association study (GWAS) to invest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b895b7ba23d6f6db69ea08dad6a2f30d
https://europepmc.org/articles/PMC4963303/