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by Olga Lomakina and Ekaterina Alekseeva and Sania Valieva and Tatiana Bzarova and Irina Nikishina and Elena Zholobova and Svetlana Rodionovskaya and Maria Kaleda and Yasuo Nakagishi and Masaki Shimizu and Mao Mizuta and Akihiro Yachie and Yuko Sugita and Nami Okamoto and Kousuke Shabana and Takuji Murata and Hiroshi Tamai and Eve M. Smith and Peng Yin and Andrea L. Jorgensen and Michael W. Beresford and on behalf of On behalf of the UK JSLE Cohort Study and Eve M. Smith and Antonio Eleuteri and Beatrice Goilav and Laura Lewandowski and Angel Phuti and Dawn Wahezi and Tamar Rubinstein and Caroline Jones and Paul Newland and Stephen Marks and Rachel Corkhill and Diana Ekdawy and Clarissa Pilkington and Kjell Tullus and Chaim Putterman and Chris Scott and Antony C. Fisher and Michael W. Beresford and Eve M. Smith and Laura Lewandowski and Angel Phuti and Andrea Jorgensen and Chris Scott and Michael W. Beresford and Ezgi Deniz Batu and Can Kosukcu and Ekim Taskiran and Sema Akman and Kubra Ozturk and Betul Sozeri and Erbil Unsal and Zelal Ekinci and Yelda Bilginer and Mehmet Alikasifoglu and Seza Ozen and Hanna Lythgoe and Michael W. Beresford and Hermine I. Brunner and Gaurav Gulati and Jordan T. Jones and Mekibib Altaye and Jamie Eaton and Mark Difrancesco and Joo Guan Yeo and Jingyao Leong and Loshinidevi D/O Thana Bathi and Thaschawee Arkachaisri and Salvatore Albani and Nagla Abdelrahman and Michael W Beresford and Valentina Leone and UK JSLE study group supported by the National Institute of Health Research Clinical Research Network and Noortje Groot and D. Shaikhani and I. E. M. Bultink and M. Bijl and R. J. E. M. Dolhain and Y. K. O. Teng and E. Zirkzee and K. de Leeuw and R. Fritsch-Stork and S. S. M. Kamphuis and Rachael D. Wright and Eve M. Smith and Michael W. Beresford and Reem Abdawani and Laila Al Shaqshi and Ibrahim Al Zakwani and Natali W. Gormezano and David Kern and Oriany L. Pereira and Gladys C. C. Esteves and Adriana M. Sallum and Nadia E. Aikawa and Rosa M. Pereira and Clovis A. Silva and Eloisa Bonfa and Jessica Beckmann and ...
PEDIATRIC RHEUMATOLOGY, ISSN 1546-0096, 05/2017, Volume 15, Issue S1, pp. 105 - 201
Journal Article
by Lomakina, Olga and Alekseeva, Ekaterina and Valieva, Sania and Bzarova, Tatiana and Nikishina, Irina and Zholobova, Elena and Rodionovskaya, Svetlana and Kaleda, Maria and Nakagishi, Yasuo and Shimizu, Masaki and Mizuta, Mao and Yachie, Akihiro and Sugita, Yuko and Okamoto, Nami and Shabana, Kousuke and Murata, Takuji and Tamai, Hiroshi and Smith, Eve M and Yin, Peng and Jorgensen, Andrea L and Beresford, Michael W and Eleuteri, Antonio and Goilav, Beatrice and Lewandowski, Laura and Phuti, Angel and Wahezi, Dawn and Rubinstein, Tamar and Jones, Caroline and Newland, Paul and Marks, Stephen and Corkhill, Rachel and Ekdawy, Diana and Pilkington, Clarissa and Tullus, Kjell and Putterman, Chaim and Scott, Chris and Fisher, Antony C and Jorgensen, Andrea and Batu, Ezgi Deniz and Kosukcu, Can and Taskiran, Ekim and Akman, Sema and Ozturk, Kubra and Sozeri, Betul and Unsal, Erbil and Ekinci, Zelal and Bilginer, Yelda and Alikasifoglu, Mehmet and Ozen, Seza and Lythgoe, Hanna and Brunner, Hermine I and Gulati, Gaurav and Jones, Jordan T and Altaye, Mekibib and Eaton, Jamie and Difrancesco, Mark and Yeo, Joo Guan and Leong, Jingyao and Bathi, Loshinidevi D/O Thana and Arkachaisri, Thaschawee and Albani, Salvatore and Abdelrahman, Nagla and Beresford, Michael W and Leone, Valentina and Groot, Noortje and Shaikhani, D and Bultink, I. E. M and Bijl, M and Dolhain, R. J. E. M and Teng, Y. K. O and Zirkzee, E and de Leeuw, K and Fritsch-Stork, R and Kamphuis, S. S. M and Wright, Rachael D and Abdawani, Reem and Al Shaqshi, Laila and Al Zakwani, Ibrahim and Gormezano, Natali W and Kern, David and Pereira, Oriany L and Esteves, Gladys C. C and Sallum, Adriana M and Aikawa, Nadia E and Pereira, Rosa M and Silva, Clovis A and Bonfa, Eloisa and Beckmann, Jessica and Bartholomä, Nora and Venhoff, Nils and Henneke, Philipp and Salzer, Ulrich and Janda, Ales and Boteanu, Alina Lucica and Corral, Sandra Garrote and Giraldo, Alberto Sifuentes and Gámir, Mariluz Gámir and Mendoza, Antonio Zea and Adrovic, Amra and Dedeoglu, Reyhan and ... and Single Hub and Access point for paediatric Rheumatology in Europe (SHARE) and Juvenile Dermatomyositis Research Group and European Federation of Immunological Societies and UK JSLE study group supported by the National Institute of Health Research Clinical Research Network and on behalf of Juvenile Dermatomyositis Research Group (JDRG) and on behalf of PRINTO and Eurofever Project and on behalf of Italian Pediatric Rheumatology Study Group and PANLAR Pediatric Rheumatology Study Group and ICON study group and on behalf of On behalf of the UK JSLE Cohort Study and the Nordic Study Group of Pediatric Rheumatology (NoSPeR) and on behalf of PRINTO and PRCSG and on behalf of the UK Juvenile Dermatomyositis Research Group (JDRG) and BIKER collaborative group and on behalf of PANLAR Pediatric Rheumatology Study Group and GRIP study group and Juvenile Inflammatory Rheumatism (JIR) Cohort and CAPS and GRANT Medical University, Sofia 68/2015 and Drug Delivery Group and for the CARRA Registry Investigators and on behalf of PRINTO and Eurofever Registry and Juvenile Dermatomyositis Research Group (JDRG) and Nordic Study Group of Pediatric Rheumatology (NoSPeR)
Pediatric Rheumatology, ISSN 1546-0096, 05/2017, Volume 15, Issue S1
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 2176 - 15
Microbial nucleic acid recognition serves as the major stimulus to an antiviral response, implying a requirement to limit the misrepresentation of self nucleic... 
AICARDI-GOUTIERES-SYNDROME | SYSTEMIC-LUPUS-ERYTHEMATOSUS | ACTIVE ENZYME | MAMMALIAN DNA | MULTIDISCIPLINARY SCIENCES | ALPHA | INFLAMMATORY DISEASE | DEOXYRIBONUCLEASE-II | MUTATIONS | EXONUCLEASE TREX1 | NUCLEIC-ACIDS | Endodeoxyribonucleases - immunology | Phosphorylation | Deoxyribonucleases - deficiency | Humans | RNA, Messenger - analysis | Male | Gene Expression Profiling | Erythroblasts - immunology | Signal Transduction - immunology | Deoxyribonucleases - immunology | STAT1 Transcription Factor - metabolism | Female | Endodeoxyribonucleases - deficiency | Child | STAT3 Transcription Factor - metabolism | Interferon-alpha - metabolism | Antiviral Agents - pharmacology | Hereditary Autoinflammatory Diseases - blood | Hereditary Autoinflammatory Diseases - enzymology | Hereditary Autoinflammatory Diseases - immunology | Interferon-alpha - immunology | Up-Regulation - drug effects | Deoxyribonucleases - genetics | Hematopoiesis - immunology | Endodeoxyribonucleases - genetics | Sequence Analysis, RNA | Interferon-alpha - blood | Adolescent | Mutation | Hereditary Autoinflammatory Diseases - genetics | Glomerulonephritis | Neonates | Deformation | Liver | Antibodies | α-Interferon | Microorganisms | Lymphocytes | Hematopoiesis | Peripheral blood | Anti-DNA antibodies | Stat1 protein | Enzyme-linked immunosorbent assay | Deoxyribonucleic acid--DNA | Deoxyribonuclease | Hematology | Anemia | Stat3 protein | Nucleic acids | Ribonucleic acid--RNA | Hemopoiesis | Signaling | Monocytes | Erythroblasts | Fibrosis | Interferon | Endonuclease | Life Sciences | Immunology
Journal Article
Diagnostics (Basel, Switzerland), ISSN 2075-4418, 09/2019, Volume 9, Issue 3, p. 113
Interferon-stimulated genes (ISGs) are a set of genes whose transcription is induced by interferon (IFN). The measure of the expression of ISGs enables... 
biostatistics | RHEUMATOID-ARTHRITIS | interferon signature score | interferonopathies | ACTIVATION | INDUCIBLE GENE-EXPRESSION | PATHOGENESIS | MEDICINE, GENERAL & INTERNAL | systemic lupus erythematosus | AICARDI-GOUTIERES-SYNDROME | inter-laboratory variability | data sharing | DIFFERENTIAL EXPRESSION ANALYSIS | PROGRAM
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, ISSN 1107-3756, 07/2019, Volume 44, Issue 1, pp. 262 - 272
Congenital disorder of glycosylation (CDG) type Ia is a multisystem disorder that occurs due to mutations in the phosphomannomutase 2 (PMM2) gene, which... 
MEDICINE, RESEARCH & EXPERIMENTAL | PMM2-CDG | PROTEIN | DRUG-DELIVERY | L-lactide-co-glycolide) nanoparticles | congenital disorder of glycosylation type Ia | enzymatic assays | CO-GLYCOLIDE-NANOPARTICLES | FIBROBLASTS | PEPTIDE | THERAPY | ENZYME | guanosine-diphosphatemannose | hypoglycosylation | poly (D | EXPRESSION | DIAGNOSTICS
Journal Article
International journal of molecular medicine, 05/2019
Congenital disorder of glycosylation (CDG) type Ia is a multisystem disorder that occurs due to mutations in the phosphomannomutase 2 (PMM2) gene, which... 
Journal Article
Revista Brasileira de Fruticultura, ISSN 0100-2945, 08/2005, Volume 27, Issue 2, pp. 277 - 280
O objetivo deste trabalho foi avaliar a germinação de sementes de Passiflora alata Curtis sob o efeito da presença de arilo em diferentes substratos de papel e... 
Journal Article
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