Genetically modified CD34+ hematopoietic stem cells contribute to turnover of brain perivascular macrophages in long-term repopulated primates. (Q37164223)

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scientific article published on 06 April 2009

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English	Genetically modified CD34+ hematopoietic stem cells contribute to turnover of brain perivascular macrophages in long-term repopulated primates.	scientific article published on 06 April 2009

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25 January 2020

Genetically modified CD34+ hematopoietic stem cells contribute to turnover of brain perivascular macrophages in long-term repopulated primates (English)

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25 January 2020

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brain perivascular macrophage

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Cynthia E. Dunbar

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Caroline Soulas

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Robert E Donahue

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Derek A Persons

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Xavier Alvarez

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Kenneth C Williams

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6 April 2009

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The American Journal of Pathology

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174

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1808-1817

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25 January 2020

Favorable outcome of ex-vivo purging of monocytes after the reintroduction of treatment after interruption in patients infected with multidrug resistant HIV-1.

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Stable reduction of CCR5 by RNAi through hematopoietic stem cell transplant in non-human primates

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Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells

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Central nervous system perivascular cells are immunoregulatory cells that connect the CNS with the peripheral immune system

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Perivascular macrophages are the primary cell type productively infected by simian immunodeficiency virus in the brains of macaques: implications for the neuropathogenesis of AIDS.

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Perivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo

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Distribution of extracellular tracers in perivascular spaces of the rat brain

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6 September 2017

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Heterogeneity of microglial and perivascular cell populations: insights gained from the facial nucleus paradigm

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Perivascular cells act as scavengers in the cerebral perivascular spaces and remain distinct from pericytes, microglia and macrophages.

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Identity of ED2-positive perivascular cells in rat brain

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CD163-positive perivascular macrophages in the human CNS express molecules for antigen recognition and presentation.

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Alpha-smooth muscle actin, a differentiation marker of smooth muscle cells, is present in microfilamentous bundles of pericytes

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Male donor-derived cells in the brains of female sex-mismatched bone marrow transplant recipients: a Y-chromosome specific in situ hybridization study

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Identifiers

10.2353/AJPATH.2009.081010

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25 January 2020

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25 January 2020

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25 January 2020

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