Publications by authors named "Philippe Burlet"

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A fertilin-derived peptide improves in vitro maturation and ploidy of human oocytes.
Amira Sallem, Anne-Lyse Denizot, Ahmed Ziyyat, Audrey L'Hostis, Sophie Favier, Philippe Burlet

F S Sci· February 2022

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Cyclic fertilin-derived peptide stimulates in vitro human embryo development.
Anne-Lyse Denizot, Audrey L'Hostis, Amira Sallem, Sophie Favier, Rémi Pierre, Philippe Burlet

F S Sci· February 2022

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Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy.
Delphine Sapaly, Matthieu Dos Santos, Perrine Delers, Olivier Biondi, Gwendoline Quérol, Philippe Burlet

Sci Rep· February 2018

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Data from artificial models of mitochondrial DNA disorders are not always applicable to humans.
Julie Steffann, Nadine Gigarel, David C Samuels, Sophie Monnot, Roxana Borghese, Philippe Burlet

Cell Rep· May 2014

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Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.
Sophie Monnot, David C Samuels, Laetitia Hesters, Nelly Frydman, Nadine Gigarel, Philippe Burlet

Hum Mol Genet· May 2013

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A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies.
Benoît Renvoisé, Gwendoline Quérol, Eloi Rémi Verrier, Philippe Burlet, Suzie Lefebvre

J Cell Sci· June 2012

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[Ten years' experience of preimplantation genetic diagnosis in Paris: remaining obstacles and potential solutions].
René Frydman, Nelly Achour-Frydman, Julie Steffann, Fredéric Lamazou, Renato Fanchin, Philippe Burlet

Bull Acad Natl Med· April 2012

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[Extending preimplantation genetic diagnosis to HLA typing: the French exception].
Julie Steffann, Nelly Frydman, Philippe Burlet, Nadine Gigarel, Laetitia Hesters

Bull Acad Natl Med· April 2012

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Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.
Nadine Gigarel, Laetitia Hesters, David C Samuels, Sophie Monnot, Philippe Burlet

Am J Hum Genet· April 2011

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Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system.
Sophie Monnot, Nadine Gigarel, David C Samuels, Philippe Burlet, Laetitia Hesters

Hum Mutat· January 2011

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Single-sperm analysis for recurrence risk assessment of spinal muscular atrophy.
Philippe Burlet, Nadine Gigarel, Maryse Magen, Séverine Drunat, Alexandra Benachi

Eur J Hum Genet· April 2010

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The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.
Benoît Renvoisé, Sabrina Colasse, Philippe Burlet, Louis Viollet, U Thomas Meier

Hum Mol Genet· April 2009

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Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophy.
Philippe Burlet, Nelly Frydman, Nadine Gigarel, Jean Paul Bonnefont, Violaine Kerbrat

Fertil Steril· September 2005

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Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR.
Nadine Gigarel, Pierre F Ray, Philippe Burlet, Nelly Frydman, Ghislaine Royer

Mol Genet Metab· March 2005

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Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations.
Olivier Clermont, Philippe Burlet, Paule Benit, Dominique Chanterau, Pascale Saugier-Veber

Hum Mutat· November 2004

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Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.
Nadine Gigarel, Nelly Frydman, Philippe Burlet, Violaine Kerbrat, Julie Steffann

Hum Genet· February 2004

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A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy.
Suzie Lefebvre, Philippe Burlet, Louis Viollet, Solange Bertrandy, Céline Huber

Hum Mol Genet· May 2002

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Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
Louis Viollet, Annie Barois, Jean G Rebeiz, Ziad Rifai, Philippe Burlet

Ann Neurol· May 2002

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