Carapito, Raphael : rechercher sur Z-Library

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1

Efficient hydrolysis of hemicellulose by a Fusarium graminearum xylanase blend produced at high levels in Escherichia coli

Raphaël Carapito, Christine Carapito, Jean-Marc Jeltsch, Vincent Phalip

Journal:

Bioresource Technology

Année:

2009

Langue:

english

Fichier:

PDF, 286 KB

english, 2009

2

ChemInform Abstract: α-L-Arabinofuranosylated Pyrrolidines as Arabinanase Inhibitors.

Ethan D. Goddard-Borger, Raphael Carapito, Jean-Marc Jeltsch, Vincent Phalip, Robert V. Stick, Annabelle Varrot

Journal:

Année:

2011

Fichier:

PDF, 23 KB

2011

3

Automated high-throughput process for site-directed mutagenesis, production, purification, and kinetic characterization of enzymes

Raphaël Carapito, Benoit Gallet, André Zapun, Thierry Vernet

Journal:

Analytical Biochemistry

Année:

2006

Langue:

english

Fichier:

PDF, 283 KB

english, 2006

4

Gene expression in Fusarium graminearum grown on plant cell wall

Raphaël Carapito, Didier Hatsch, Sonja Vorwerk, Elizabet Petkovski, Jean-Marc Jeltsch, Vincent Phalip

Journal:

Fungal Genetics and Biology

Année:

2008

Langue:

english

Fichier:

PDF, 287 KB

english, 2008

5

Genome-wide transcriptional responses of Fusarium graminearum to plant cell wall substrates

Carapito, Raphaël, Vorwerk, Sonja, Jeltsch, Jean-Marc, Phalip, Vincent

Journal:

FEMS Microbiology Letters

Année:

2013

Langue:

english

Fichier:

PDF, 350 KB

english, 2013

6

High diversity ofMICgenes in non-human primates

Alice Meyer,Raphael Carapito,Louise Ott,Mirjana Radosavljevic…

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 1.76 MB

english, 2014

7

α-l-Arabinofuranosylated pyrrolidines as arabinanase inhibitors

Goddard-Borger, Ethan D., Carapito, Raphael, Jeltsch, Jean-Marc, Phalip, Vincent, Stick, Robert V., Varrot, Annabelle

Journal:

Chemical Communications

Année:

2011

Langue:

english

Fichier:

PDF, 1.25 MB

english, 2011

8

Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritis

Meyer, Alain, Lannes, Béatrice, Carapito, Raphaël, Bahram, Seiamak, Echaniz-Laguna, Andoni, Geny, Bernard, Sibilia, Jean, Gottenberg, Jacques Eric

Journal:

Neuromuscular Disorders

Année:

2015

Langue:

english

Fichier:

PDF, 1.41 MB

english, 2015

9

A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions

Carapito, Raphael, Paul, Nicodème, Untrau, Meiggie, Ott, Louise, Corradini, Nadège, Poignant, Sylvaine, Geffroy, Loïc, Caldagues, Emmanuelle, Heymann, Marie-Françoise, Cassagnau, Elisabeth, Isidor, Be

Journal:

Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 741 KB

english, 2014

10

On the genetics of the Silk Route: association analysis of HLA,IL10, andIL23R-IL12RB2regions with Behçet’s disease in an Iranian population

Carapito, Raphael, Shahram, Farhad, Michel, Sandra, Le Gentil, Marion, Radosavljevic, Mirjana, Meguro, Akira, Abdollahi, Bahar Sadeghi, Inoko, Hidetoshi, Ota, Masao, Davatchi, Fereydoun, Bahram, Seiam

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 152 KB

english, 2015

11

Next-Generation Sequencing of the HLA locus: methods and impacts on HLA typing, population genetics and disease association studies

Carapito, Raphael, Radosavljevic, Mirjana, Bahram, Seiamak

Journal:

Human Immunology

Année:

2016

Langue:

english

Fichier:

PDF, 810 KB

english, 2016

12

Genetics, genomics, and evolutionary biology of NKG2D ligands

Carapito, Raphael, Bahram, Seiamak

Journal:

Immunological Reviews

Année:

2015

Langue:

english

Fichier:

PDF, 2.07 MB

english, 2015

13

Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome

Carapito, Raphael, Goldenberg, Alice, Paul, Nicodème, Pichot, Angélique, David, Albert, Hamel, Antoine, Dumant-Forest, Clémentine, Leroux, Julien, Ory, Benjamin, Isidor, Bertrand, Bahram, Seiamak

Journal:

European Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 1.19 MB

english, 2016

14

A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia

Carapito, Raphael, Paul, Nicodème, Untrau, Meiggie, Le Gentil, Marion, Ott, Louise, Alsaleh, Ghada, Jochem, Pierre, Radosavljevic, Mirjana, Le Caignec, Cédric, David, Albert, Damier, Philippe, Isidor,

Journal:

Movement Disorders

Année:

2015

Langue:

english

Fichier:

PDF, 916 KB

english, 2015

15

The TRANSPLANTEX initiative

Bahram, Seiamak, Carapito, Raphael, Gourraud, Pierre-Antoine, Charron, Dominique

Journal:

Human Immunology

Année:

2016

Langue:

english

Fichier:

PDF, 303 KB

english, 2016

16

A new MHC-linked susceptibility locus for primary Sjögren’s syndrome: MICA

Carapito, Raphael, Gottenberg, Jacques-Eric, Kotova, Irina, Untrau, Meiggie, Michel, Sandra, Naegely, Lydie, Aouadi, Ismail, Kwemou, Marius, Paul, Nicodème, Pichot, Angélique, Locke, James, Bowman, Si

Journal:

Human Molecular Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 1.38 MB

english, 2017

17

Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)

Messer, Laurent, Alsaleh, Ghada, Georgel, Philippe, Carapito, Raphael, Waterham, Hans R, Dali-Youcef, Nassim, Bahram, Siamak, Sibilia, Jean

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 674 KB

english, 2016

18

A novel zebrafish model of congenital neutropenia

Konantz, Martina, Müller, Joëlle, Alghisi, Elisa, Carapito, Raphaël, Bahram, Seiamak, Lengerke, Claudia

Journal:

Experimental Hematology

Année:

2017

Langue:

english

Fichier:

PDF, 180 KB

english, 2017

19

Natural Killer Group 2, Member D/NKG2D Ligands in Hematopoietic Cell Transplantation

Carapito, Raphael, Aouadi, Ismail, Ilias, Wassila, Bahram, Seiamak

Journal:

Frontiers in Immunology

Année:

2017

Langue:

english

Fichier:

PDF, 761 KB

english, 2017

20

Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency

Carapito, Raphael, Carapito, Christine, Morlon, Aurore, Paul, Nicodème, Vaca Jacome, Alvaro Sebastian, Alsaleh, Ghada, Rolli, Véronique, Tahar, Ouria, Aouadi, Ismail, Rompais, Magali, Delalande, Franç

Journal:

Annals of the Rheumatic Diseases

Année:

2018

Langue:

english

Fichier:

PDF, 3.75 MB

english, 2018

21

An unusually high substitution rate in transplant-associated BK polyomavirus in vivo is further concentrated in HLA-C-bound viral peptides

Domingo-Calap, Pilar, Schubert, Benjamin, Joly, Mélanie, Solis, Morgane, Untrau, Meiggie, Carapito, Raphael, Georgel, Philippe, Caillard, Sophie, Fafi-Kremer, Samira, Paul, Nicodème, Kohlbacher, Olive

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 1.88 MB

english, 2018

22

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

Carapito, Raphael, Ivanova, Ekaterina L., Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine,

Journal:

The American Journal of Human Genetics

Année:

2019

Langue:

english

Fichier:

PDF, 1.89 MB

english, 2019

23

HLA*LA – HLA typing from linearly projected graph alignments

Dilthey, Alexander T, Mentzer, Alexander J, Carapito, Raphael, Cutland, Clare, Cereb, Nezih, Madhi, Shabir A, Rhie, Arang, Koren, Sergey, Bahram, Seiamak, McVean, Gil, Phillippy, Adam M, Berger, Bonni

Journal:

Année:

2019

Langue:

english

Fichier:

PDF, 240 KB

english, 2019

24

Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitis

Molitor, Anne, Prud’homme, Tony, Miao, Zhichao, Conrad, Solène, Bloch-Zupan, Agnès, Pichot, Angélique, Hanauer, Antoine, Isidor, Bertrand, Bahram, Seiamak, Carapito, Raphael

Journal:

Journal of Human Genetics

Année:

2019

Fichier:

PDF, 1.05 MB

2019

25

IKZF1 Loss-of-Function Variant Causes Autoimmunity and Severe Familial Antiphospholipid Syndrome

Dieudonné, Yannick, Guffroy, Aurélien, Vollmer, Olivier, Carapito, Raphael, Korganow, Anne-Sophie

Journal:

Journal of Clinical Immunology

Année:

2019

Langue:

english

Fichier:

PDF, 658 KB

english, 2019

26

IKZF1 Loss-of-Function Variant Causes Autoimmunity and Severe Familial Antiphospholipid Syndrome

Dieudonné, Yannick, Guffroy, Aurélien, Vollmer, Olivier, Carapito, Raphael, Korganow, Anne-Sophie

Journal:

Journal of Clinical Immunology

Année:

2019

Fichier:

PDF, 658 KB

2019

27

Update on Fc-Mediated Antibody Functions Against HIV-1 Beyond Neutralization

Su, Bin, Dispinseri, Stefania, Iannone, Valeria, Zhang, Tong, Wu, Hao, Carapito, Raphael, Bahram, Seiamak, Scarlatti, Gabriella, Moog, Christiane

Journal:

Frontiers in Immunology

Année:

2019

Langue:

english

Fichier:

PDF, 1.07 MB

english, 2019

28

Update on Fc-Mediated Antibody Functions Against HIV-1 Beyond Neutralization

Su, Bin, Dispinseri, Stefania, Iannone, Valeria, Zhang, Tong, Wu, Hao, Carapito, Raphael, Bahram, Seiamak, Scarlatti, Gabriella, Moog, Christiane

Journal:

Frontiers in Immunology

Année:

2019

Fichier:

PDF, 1.07 MB

2019

29

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

Carapito, Raphael, Ivanova, Ekaterina L., Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine,

Journal:

The American Journal of Human Genetics

Année:

2020

Fichier:

PDF, 29 KB

2020

30

A mouse model of MSU-induced acute inflammation in vivo suggests imiquimod-dependent targeting of Il-1Î² as relevant therapy for gout patients

Mariotte, Alexandre, De Cauwer, Aurore, Po, Chrystelle, Abou-Faycal, ChÃ©rine, Pichot, AngÃ©lique, Paul, NicodÃ¨me, Aouadi, Ismael, Carapito, Raphael, Frisch, Benoit, Macquin, CÃ©cile, Chatelus, Emman

Journal:

Année:

2020

Fichier:

PDF, 2.06 MB

2020

31

High-Throughput MICA/B Genotyping of Over Two Million Samples: Workflow and Allele Frequencies

Klussmeier, Anja, Massalski, Carolin, Putke, Kathrin, SchÃ¤fer, Gesine, Sauter, JÃ¼rgen, Schefzyk, Daniel, Pruschke, Jens, Hofmann, Jan, FÃ¼rst, Daniel, Carapito, Raphael, Bahram, Seiamak, Schmidt, Al

Journal:

Frontiers in Immunology

Année:

2020

Fichier:

PDF, 835 KB

2020

32

Matrix-Targeting Immunotherapy Controls Tumor Growth and Spread by Switching Macrophage Phenotype

Deligne, Claire, Murdamoothoo, Devadarssen, Gammage, AnÃs N., Gschwandtner, Martha, Erne, William, Loustau, Thomas, Marzeda, Anna M., Carapito, Raphael, Paul, NicodÃ¨me, Velazquez-Quesada, InÃ©s, Maz

Journal:

Cancer Immunology Research

Année:

2020

Langue:

english

Fichier:

PDF, 1.94 MB

english, 2020

33

Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV status

Carapito, Raphael, Aouadi, Ismail, Pichot, AngÃ©lique, Spinnhirny, Perrine, Morlon, Aurore, Kotova, Irina, Macquin, CÃ©cile, Rolli, VÃ©ronique, Cesbron, Anne, Gagne, Katia, Oudshoorn, Machteld, van de

Journal:

Bone Marrow Transplantation

Année:

2020

Fichier:

PDF, 1.33 MB

2020

34

A FcÉ£RIIa polymorphism has a HLA-B57 and HLA-B27 independent effect on HIV disease outcome

Carapito, Raphael, Mayr, Luzia, Molitor, Anne, Verniquet, Martin, Schmidt, Sylvie, Tahar, Ouria, Partisani, Marialuisa, Rey, David, Lambotte, Olivier, Bahram, Seiamak, Moog, Christiane

Journal:

Genes and Immunity

Année:

2020

Fichier:

PDF, 440 KB

2020

35

Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants

Khan, Amjad, Miao, Zhichao, Umair, Muhammad, Ullah, Amir, Alshabeeb, Mohammad A., Bilal, Muhammad, Ahmad, Farooq, Rappold, Gudrun A., Ansar, Muhammad, Carapito, Raphael

Journal:

Année:

2020

Fichier:

PDF, 1.48 MB

2020

36

Improvement of therapy-induced myelodysplastic syndrome by infusion of autologous CD34-positive hematopoietic progenitor cells without chemotherapy

Alary, Anne-Sophie, Vignon, Marguerite, Carapito, Raphael, Halabi, Najeeb, Willems, Lise, Green, Alexa, Chapuis, Nicolas, Heshmati, Farhad, Cuccuini, Wendy, Kaltenbach, Sophie, Radford-Weiss, Isabelle

Journal:

Leukemia and Lymphoma

Année:

2020

Fichier:

PDF, 1.04 MB

2020

37

A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report

Jacob, Arthur, Pasquier, Jennifer, Carapito, Raphael, AuradÃ©, FrÃ©dÃ©ric, Molitor, Anne, Froguel, Philippe, Fakhro, Khalid, Halabi, Najeeb, Viot, GÃ©raldine, Bahram, Seiamak, Rafii, Arash

Journal:

BMC Medical Genetics

Année:

2020

Fichier:

PDF, 1.62 MB

2020

38

Structural and Functional Impact of SRP54 Mutations Causing Severe Congenital Neutropenia

Juaire, Keven D., Lapouge, Karine, Becker, Matthias M.M., Kotova, Irina, Michelhans, Michelle, Carapito, Raphael, Wild, Klemens, Bahram, Seiamak, Sinning, Irmgard

Journal:

Année:

2020

Fichier:

PDF, 3.87 MB

2020

39

NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation

Castro, Carla Noemi, Rosenzwajg, Michelle, Carapito, Raphael, Shahrooei, Mohammad, Konantz, Martina, Khan, Amjad, Miao, Zhichao, GroÃ, Miriam, Tranchant, Thibaud, Radosavljevic, Mirjana, Paul, NicodÃ

Journal:

Journal of Experimental Medicine

Année:

2020

Fichier:

PDF, 5.12 MB

2020