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STAT1 (Czech Wikipedia)

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

Last modified:

Ref.Un. Ref.Website
Global rank Czech rank
65worldcat.org
4th place
2nd place
65doi.org
2nd place
4th place
33nih.gov
5th place
8th place
22nature.com
207th place
89th place
22web.archive.org
1st place
1st place
21springer.com
182nd place
137th place
11genecards.org
low place
low place
11uniprot.org
2,402nd place
4,283rd place
11jci.org
low place
7,634th place

doi.org (Global: 2nd place; Czech: 4th place)

  • 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.

genecards.org (Global: low place; Czech: low place)

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

jci.org (Global: low place; Czech: 7,634th place)

  • 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)

nature.com (Global: 207th place; Czech: 89th place)

  • 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.

nih.gov (Global: 5th place; Czech: 8th place)

ncbi.nlm.nih.gov

  • 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)

springer.com (Global: 182nd place; Czech: 137th place)

link.springer.com

  • 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)

uniprot.org (Global: 2,402nd place; Czech: 4,283rd place)

  • 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)

web.archive.org (Global: 1st place; Czech: 1st place)

  • 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)

worldcat.org (Global: 4th place; Czech: 2nd place)

  • 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)