STAT1 (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "STAT1" in Czech language version.

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BARIS, Safa; ALROQI, Fayhan; KIYKIM, Ayca. Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1. Journal of Clinical Immunology. 2016-10-01, roč. 36, čís. 7, s. 641–648. Dostupné online [cit. 2017-08-29]. ISSN 0271-9142. doi:10.1007/s10875-016-0312-3. (anglicky)
KATZE, Michael G.; HE, Yupeng; GALE, Michael. Viruses and interferon: a fight for supremacy. Nature Reviews Immunology. Roč. 2, čís. 9, s. 675–687. Dostupné online. doi:10.1038/nri888.
CHAPGIER, Ariane; KONG, Xiao-Fei; BOISSON-DUPUIS, Stéphanie. A partial form of recessive STAT1 deficiency in humans. Journal of Clinical Investigation. 2009-06-01, roč. 119, čís. 6, s. 1502–1514. Dostupné online [cit. 2017-08-29]. ISSN 0021-9738. doi:10.1172/jci37083. (anglicky)
TOUBIANA, Julie; OKADA, Satoshi; HILLER, Julia. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood. 2016-06-23, roč. 127, čís. 25, s. 3154–3164. PMID: 27114460. Dostupné v archivu pořízeném dne 26-06-2016. ISSN 0006-4971. doi:10.1182/blood-2015-11-679902. PMID 27114460. (anglicky)
DUPUIS, Stéphanie; JOUANGUY, Emmanuelle; AL-HAJJAR, Sami. Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency. Nature Genetics. Roč. 33, čís. 3, s. 388–391. Dostupné online. doi:10.1038/ng1097.

DATABASE, GeneCards Human Gene. IRF9 Gene - GeneCards | IRF9 Protein | IRF9 Antibody. www.genecards.org [online]. [cit. 2017-08-29]. Dostupné online.

CHAPGIER, Ariane; KONG, Xiao-Fei; BOISSON-DUPUIS, Stéphanie. A partial form of recessive STAT1 deficiency in humans. Journal of Clinical Investigation. 2009-06-01, roč. 119, čís. 6, s. 1502–1514. Dostupné online [cit. 2017-08-29]. ISSN 0021-9738. doi:10.1172/jci37083. (anglicky)

KATZE, Michael G.; HE, Yupeng; GALE, Michael. Viruses and interferon: a fight for supremacy. Nature Reviews Immunology. Roč. 2, čís. 9, s. 675–687. Dostupné online. doi:10.1038/nri888.
DUPUIS, Stéphanie; JOUANGUY, Emmanuelle; AL-HAJJAR, Sami. Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency. Nature Genetics. Roč. 33, čís. 3, s. 388–391. Dostupné online. doi:10.1038/ng1097.

STAT1 signal transducer and activator of transcription 1 [Homo sapiens (human)] - Gene - NCBI. www.ncbi.nlm.nih.gov [online]. [cit. 2017-08-29]. Dostupné online.
LU, Hsu-Fung; YANG, Jai-Sing; LIN, Yuh-Tzy. Diallyl disulfide induced signal transducer and activator of transcription 1 expression in human colon cancer colo 205 cells using differential display RT-PCR. Cancer Genomics & Proteomics. March 2007, roč. 4, čís. 2, s. 93–97. PMID: 17804871. Dostupné online [cit. 2017-08-29]. ISSN 1109-6535. PMID 17804871.
TOUBIANA, Julie; OKADA, Satoshi; HILLER, Julia. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood. 2016-06-23, roč. 127, čís. 25, s. 3154–3164. PMID: 27114460. Dostupné v archivu pořízeném dne 26-06-2016. ISSN 0006-4971. doi:10.1182/blood-2015-11-679902. PMID 27114460. (anglicky)

BARIS, Safa; ALROQI, Fayhan; KIYKIM, Ayca. Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1. Journal of Clinical Immunology. 2016-10-01, roč. 36, čís. 7, s. 641–648. Dostupné online [cit. 2017-08-29]. ISSN 0271-9142. doi:10.1007/s10875-016-0312-3. (anglicky)

STAT1 - Signal transducer and activator of transcription 1-alpha/beta - Homo sapiens (Human) - STAT1 gene & protein. www.uniprot.org [online]. [cit. 2017-08-29]. Dostupné online. (anglicky)

USER, Super. Defects of STAT1 in Human. Loss of Function exposes to Mycobacteria. Gain of Function exposes to Candida. www.asid.ma [online]. [cit. 2017-08-29]. Dostupné v archivu pořízeném dne 2017-08-29. (anglicky)
TOUBIANA, Julie; OKADA, Satoshi; HILLER, Julia. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood. 2016-06-23, roč. 127, čís. 25, s. 3154–3164. PMID: 27114460. Dostupné v archivu pořízeném dne 26-06-2016. ISSN 0006-4971. doi:10.1182/blood-2015-11-679902. PMID 27114460. (anglicky)

BARIS, Safa; ALROQI, Fayhan; KIYKIM, Ayca. Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1. Journal of Clinical Immunology. 2016-10-01, roč. 36, čís. 7, s. 641–648. Dostupné online [cit. 2017-08-29]. ISSN 0271-9142. doi:10.1007/s10875-016-0312-3. (anglicky)
LU, Hsu-Fung; YANG, Jai-Sing; LIN, Yuh-Tzy. Diallyl disulfide induced signal transducer and activator of transcription 1 expression in human colon cancer colo 205 cells using differential display RT-PCR. Cancer Genomics & Proteomics. March 2007, roč. 4, čís. 2, s. 93–97. PMID: 17804871. Dostupné online [cit. 2017-08-29]. ISSN 1109-6535. PMID 17804871.
Primary immunodeficiency diseases : definition, diagnosis, and management. Second edition. vyd. Berlin, Germany: [s.n.] 1 online resource s. ISBN 9783662529096. OCLC 965196110
CHAPGIER, Ariane; KONG, Xiao-Fei; BOISSON-DUPUIS, Stéphanie. A partial form of recessive STAT1 deficiency in humans. Journal of Clinical Investigation. 2009-06-01, roč. 119, čís. 6, s. 1502–1514. Dostupné online [cit. 2017-08-29]. ISSN 0021-9738. doi:10.1172/jci37083. (anglicky)
TOUBIANA, Julie; OKADA, Satoshi; HILLER, Julia. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood. 2016-06-23, roč. 127, čís. 25, s. 3154–3164. PMID: 27114460. Dostupné v archivu pořízeném dne 26-06-2016. ISSN 0006-4971. doi:10.1182/blood-2015-11-679902. PMID 27114460. (anglicky)