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Jean-Michel Heard

Researcher at French Institute of Health and Medical Research

Publications -  18
Citations -  1910

Jean-Michel Heard is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Virus & Bone marrow. The author has an hindex of 14, co-authored 18 publications receiving 1864 citations. Previous affiliations of Jean-Michel Heard include Centre national de la recherche scientifique.

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A putative truncated cytokine receptor gene transduced by the myeloproliferative leukemia virus immortalizes hematopoietic progenitors.

TL;DR: It is shown that in vitro infection of bone marrow cells with helper-free MPLV readily yields immortalized factor-independent hematopoietic cell lines of different lineages.
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Retroviral-mediated gene transfer into hepatocytes in vivo.

TL;DR: In rats, retroviral-mediated gene transfer with a surgical procedure in which the liver is temporarily excluded from the circulation and infected in vivo is combined to provide a feasible alternative to in vitro reimplantation of genetically modified hepatocytes.
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Human immunodeficiency virus type 1 entry into macrophages mediated by macropinocytosis.

TL;DR: Observations in human primary macrophages provide new insights into HIV-1 interactions with a cell target relevant to pathogenesis and may have implications for the design of soluble inhibitors aimed at interfering with the fusion or entry processes.
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Intracerebral administration of adeno-associated viral vector serotype rh.10 carrying human SGSH and SUMF1 cDNAs in children with mucopolysaccharidosis type IIIA disease: results of a phase I/II trial.

TL;DR: Four children (Patients 1–3, aged between 5.5 and 6 years; Patient 4 aged 2 years 8 months) received intracerebral injections of an adeno-associated viral vector serotype rh.10-SGSH-IRES-SUMF1 vector in a phase I/II clinical trial, with promising results.
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Antiviral Activity of the Proteasome on Incoming Human Immunodeficiency Virus Type 1

TL;DR: It is shown that treatment of target cells with the proteasome inhibitors MG132 and lactacystin increased the efficiency of HIV infection and degradation of incoming viral proteins by the proteAsome represents an early intracellular defense against infection.