Literature DB >> 19203666

Signal transducer and activator of transcription 5 tyrosine phosphorylation for the diagnosis and monitoring of patients with severe combined immunodeficiency.

Denise Walshe, H Bobby Gaspar, Adrian J Thrasher, Catherine M Cale, Kimberly C Gilmour.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19203666     DOI: 10.1016/j.jaci.2008.11.041

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


× No keyword cloud information.
  6 in total

Review 1.  Advances in basic and clinical immunology in 2009.

Authors:  Javier Chinen; William T Shearer
Journal:  J Allergy Clin Immunol       Date:  2010-03       Impact factor: 10.793

2.  The IL-2RG R328X nonsense mutation allows partial STAT-5 phosphorylation and defines a critical region involved in the leaky-SCID phenotype.

Authors:  A Arcas-García; M Garcia-Prat; M Magallón-Lorenz; A Martín-Nalda; O Drechsel; S Ossowski; L Alonso; J G Rivière; P Soler-Palacín; R Colobran; J Sayós; M Martínez-Gallo; C Franco-Jarava
Journal:  Clin Exp Immunol       Date:  2020-01-19       Impact factor: 4.330

Review 3.  Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency.

Authors:  Mirjam van der Burg; Andy R Gennery
Journal:  Eur J Pediatr       Date:  2011-04-09       Impact factor: 3.183

4.  Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.

Authors:  Rojeen Shahni; Catherine M Cale; Glenn Anderson; Laura D Osellame; Sophie Hambleton; Thomas S Jacques; Yehani Wedatilake; Jan-Willem Taanman; Emma Chan; Waseem Qasim; Vincent Plagnol; Annapurna Chalasani; Michael R Duchen; Kimberly C Gilmour; Shamima Rahman
Journal:  Brain       Date:  2015-06-29       Impact factor: 13.501

5.  A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients.

Authors:  Lucila A Barreiros; Gesmar R S Segundo; Anete S Grumach; Pérsio Roxo-Júnior; Troy R Torgerson; Hans D Ochs; Antonio Condino-Neto
Journal:  Front Pediatr       Date:  2018-08-20       Impact factor: 3.418

6.  JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene.

Authors:  Gigliola Di Matteo; Maria Chiriaco; Alessia Scarselli; Cristina Cifaldi; Susanna Livadiotti; Silvia Di Cesare; Valentina Ferradini; Alessandro Aiuti; Paolo Rossi; Andrea Finocchi; Caterina Cancrini
Journal:  Mol Genet Genomic Med       Date:  2018-07-21       Impact factor: 2.183

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.