3 Papers
Ling Yun is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Biology & Gene. The author has an hindex of 3, co-authored 3 publications. Previous affiliations of Ling Yun include Paris Descartes University.
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Papers
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey.
Marie-Olivia Chandesris,Isabelle Melki,Angels Natividad,Anne Puel,Claire Fieschi,Ling Yun,Caroline Thumerelle,Eric Oksenhendler,David Boutboul,Caroline Thomas,Cyrille Hoarau,Yvon Lebranchu,Jean-Louis Stephan,Celine Cazorla,Nathalie Aladjidi,Marguerite Micheau,Fran cois Tron,André Baruchel,Vincent Barlogis,Gilles Palenzuela,Catherine Mathey,Stephane Dominique,Gerard Body,Martine Munzer,Fanny Fouyssac,Rolland Jaussaud,Brigitte Bader-Meunier,Nizar Mahlaoui,Stéphane Blanche,Marianne Debré,Muriel Le Bourgeois,Virginie Gandemer,Nathalie Lambert,Virginie Grandin,Stephanie Ndaga,Corinne Jacques,Chantal Harre,Monique Forveille,Marie-Alexandra Alyanakian,Anne Durandy,Christine Bodemer,Felipe Suarez,Olivier Hermine,Olivier Lortholary,Jean-Laurent Casanova,Alain Fischer,Capucine Picard +46 more
TL;DR: The prognosis of STAT3 deficiency may be considered good, provided that multiple prophylactic measures, including IgG infusions, are implemented, as demonstrated by the large decrease in pneumonia recurrence.
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Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.
Romain Lévy,Romain Lévy,Romain Lévy,Satoshi Okada,Satoshi Okada,Vivien Béziat,Vivien Béziat,Kunihiko Moriya,Kunihiko Moriya,Caini Liu,Louis Yi Ann Chai,Louis Yi Ann Chai,Mélanie Migaud,Mélanie Migaud,Fabian Hauck,Amein Al Ali,Cyril Cyrus,Chittibabu Vatte,Turkan Patiroglu,Ekrem Unal,Marie Ferneiny,Nobuyuki Hyakuna,Serdar Nepesov,Matías Oleastro,Aydan Ikinciogullari,Figen Dogu,Takaki Asano,Osamu Ohara,Ling Yun,Ling Yun,Erika Della Mina,Erika Della Mina,Didier Bronnimann,Didier Bronnimann,Yuval Itan,Florian Gothe,Jacinta Bustamante,Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Natalia Tahuil,Caner Aytekin,Aicha Salhi,Saleh Al Muhsen,Masao Kobayashi,Julie Toubiana,Laurent Abel,Laurent Abel,Laurent Abel,Xiaoxia Li,Yildiz Camcioglu,Fatih Celmeli,Christoph Klein,Suzan A AlKhater,Jean-Laurent Casanova,Anne Puel,Anne Puel,Anne Puel +57 more
TL;DR: Twenty-one patients from 12 unrelated kindreds, homozygous for 12 different mutant alleles that underlie AR IL-17RA deficiency are reported, including this first patient.
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Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity
Laura Israel,Laura Israel,Ying Wang,Katarzyna Bulek,Erika Della Mina,Erika Della Mina,Zhao Zhang,Vincent Pedergnana,Vincent Pedergnana,Maya Chrabieh,Maya Chrabieh,Nicole Lemmens,Vanessa Sancho-Shimizu,Marc Descatoire,Théo Lasseau,Théo Lasseau,Elisabeth Israelsson,Lazaro Lorenzo,Lazaro Lorenzo,Ling Yun,Ling Yun,Aziz Belkadi,Aziz Belkadi,Andrew Moran,Leonard E. Weisman,François Vandenesch,Frédéric Batteux,Sandra K. Weller,Michael Levin,Jethro Herberg,Avinash Abhyankar,Carolina Prando,Yuval Itan,Willem J. B. van Wamel,Capucine Picard,Laurent Abel,Laurent Abel,Laurent Abel,Damien Chaussabel,Xiaoxia Li,Bruce Beutler,Peter D. Arkwright,Jean-Laurent Casanova,Anne Puel,Anne Puel,Anne Puel +45 more
TL;DR: In this paper, the authors describe eight related individuals with autosomal recessive TIRAP deficiency, who developed life-threatening staphylococcal disease during childhood in the proband, but not in the other seven homozygotes.
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