Publications by authors named "Jerome Feldmann"

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H
HIV-1 Virological Synapse: Live Imaging of Transmission.
Jerome Feldmann, Olivier Schwartz

Viruses· August 2010

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Tetherin restricts productive HIV-1 cell-to-cell transmission.
Nicoletta Casartelli, Marion Sourisseau, Jerome Feldmann, Florence Guivel-Benhassine, Adeline Mallet

PLoS Pathog· June 2010

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Direct relationship between virus load and systemic immune activation in HIV-2 infection.
Aleksandra Leligdowicz, Jérôme Feldmann, Assan Jaye, Matthew Cotten, Tao Dong

J Infect Dis· January 2010

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Downregulation of the T-cell receptor by human immunodeficiency virus type 2 Nef does not protect against disease progression.
Jérôme Feldmann, Aleksandra Leligdowicz, Assan Jaye, Tao Dong, Hilton Whittle

J Virol· December 2009

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Simultaneous cell-to-cell transmission of human immunodeficiency virus to multiple targets through polysynapses.
Dominika Rudnicka, Jérôme Feldmann, Françoise Porrot, Steve Wietgrefe, Stéphanie Guadagnini

J Virol· June 2009

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Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4.
Mickaël M Ménager, Gaël Ménasché, Maryse Romao, Perrine Knapnougel, Chen-Hsuan Ho, Jérôme Feldmann

Nat Immunol· March 2007

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Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity.
Jérôme Feldmann, Gaël Ménasché, Isabelle Callebaut, Véronique Minard-Colin, Brigitte Bader-Meunier

Blood· April 2005

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Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis.
Gael Ménasché, Jérôme Feldmann, Alain Fischer, Geneviève de Saint Basile

Immunol Rev· February 2005

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Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene.
João C S Bizario, Jérôme Feldmann, Fabíola A Castro, Gaël Ménasché, Cristina M A Jacob

J Clin Immunol· July 2004

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Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU.
Bénédicte Neven, Isabelle Callebaut, Anne-Marie Prieur, Jérôme Feldmann, Christine Bodemer

Blood· April 2004

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[Munc13-4 is essential for cytolytic granule fusion].
Jérôme Feldmann, Françoise Le Deist, Alain Fischer, Geneviève de Saint Basile

Med Sci (Paris)· February 2004

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Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Jérôme Feldmann, Isabelle Callebaut, Graça Raposo, Stéphanie Certain, Delphine Bacq

Cell· November 2003

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Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
Gaël Ménasché, Chen Hsuan Ho, Ozden Sanal, Jérôme Feldmann, Ilhan Tezcan

J Clin Invest· August 2003

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Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients.
Gaël Menasche, Jérôme Feldmann, Anne Houdusse, Catherine Desaymard, Alain Fischer

Blood· April 2003

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Selective inhibition of dipeptidyl peptidase I, not caspases, prevents the partial processing of procaspase-3 in CD3-activated human CD8(+) T lymphocytes.
Nicolas Bidère, Marie Briet, Antoine Dürrbach, Céline Dumont, Jérôme Feldmann

J Biol Chem· August 2002

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Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.
Jérôme Feldmann, Anne-Marie Prieur, Pierre Quartier, Patrick Berquin, Stephanie Certain

Am J Hum Genet· July 2002

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Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.
Jérôme Feldmann, Françoise Le Deist, Marie Ouachée-Chardin, Stéphanie Certain, Sarah Alexander

Br J Haematol· June 2002

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