Regulator cistično fibrozne transmembranske provodnosti (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Regulator cistično fibrozne transmembranske provodnosti" in Serbian language version.

refsWebsite

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10nih.gov

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8doi.org

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3harvard.edu

18^th place

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2web.archive.org

1^st place

1univ-montp2.fr

low place

1archive.org

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1sickkids.on.ca

low place

archive.org

Prasad AB, Allard MW, Green ED (2008). „Confirming the phylogeny of mammals by use of large comparative sequence data sets”. Mol. Biol. Evol. 25 (9): 1795—808. PMC 2515873 . PMID 18453548. doi:10.1093/molbev/msn104.

doi.org

Gadsby DC, Vergani P, Csanády L (2006). „The ABC protein turned chloride channel whose failure causes cystic fibrosis”. Nature. 440 (7083): 477—83. Bibcode:2006Natur.440..477G. PMID 16554808. doi:10.1038/nature04712.
Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N (septembar 1989). „Identification of the cystic fibrosis gene: chromosome walking and jumping”. Science. 245 (4922): 1059—65. Bibcode:1989Sci...245.1059R. PMID 2772657. doi:10.1126/science.2772657.
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL (1989). „Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA”. Science. 245 (4922): 1066—73. Bibcode:1989Sci...245.1066R. PMID 2475911. doi:10.1126/science.2475911.
Childers M, Eckel G, Himmel A, Caldwell J (2007). „A new model of cystic fibrosis pathology: lack of transport of glutathione and its thiocyanate conjugates”. Med. Hypotheses. 68 (1): 101—12. PMID 16934416. doi:10.1016/j.mehy.2006.06.020.
Prasad AB, Allard MW, Green ED (2008). „Confirming the phylogeny of mammals by use of large comparative sequence data sets”. Mol. Biol. Evol. 25 (9): 1795—808. PMC 2515873 . PMID 18453548. doi:10.1093/molbev/msn104.
Rowe SM, Miller S, Sorscher EJ (maj 2005). „Cystic fibrosis”. N. Engl. J. Med. 352 (19): 1992—2001. PMID 15888700. doi:10.1056/NEJMra043184.
Araújo FG, Novaes FC, Santos NP, Martins VC, Souza SM, Santos SE, Ribeiro-dos-Santos AK (januar 2005). „Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil”. Braz. J. Med. Biol. Res. 38 (1): 11—5. PMID 15665983. doi:10.1590/S0100-879X2005000100003.
Short DB, Trotter KW, Reczek D, Kreda SM, Bretscher A, Boucher RC, Stutts MJ, Milgram SL (jul 1998). „An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton”. J. Biol. Chem. 273 (31): 19797—801. PMID 9677412. doi:10.1074/jbc.273.31.19797.

harvard.edu

adsabs.harvard.edu

Gadsby DC, Vergani P, Csanády L (2006). „The ABC protein turned chloride channel whose failure causes cystic fibrosis”. Nature. 440 (7083): 477—83. Bibcode:2006Natur.440..477G. PMID 16554808. doi:10.1038/nature04712.
Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N (septembar 1989). „Identification of the cystic fibrosis gene: chromosome walking and jumping”. Science. 245 (4922): 1059—65. Bibcode:1989Sci...245.1059R. PMID 2772657. doi:10.1126/science.2772657.
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL (1989). „Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA”. Science. 245 (4922): 1066—73. Bibcode:1989Sci...245.1066R. PMID 2475911. doi:10.1126/science.2475911.

nih.gov

ncbi.nlm.nih.gov

Gadsby DC, Vergani P, Csanády L (2006). „The ABC protein turned chloride channel whose failure causes cystic fibrosis”. Nature. 440 (7083): 477—83. Bibcode:2006Natur.440..477G. PMID 16554808. doi:10.1038/nature04712.
Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N (septembar 1989). „Identification of the cystic fibrosis gene: chromosome walking and jumping”. Science. 245 (4922): 1059—65. Bibcode:1989Sci...245.1059R. PMID 2772657. doi:10.1126/science.2772657.
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL (1989). „Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA”. Science. 245 (4922): 1066—73. Bibcode:1989Sci...245.1066R. PMID 2475911. doi:10.1126/science.2475911.
Childers M, Eckel G, Himmel A, Caldwell J (2007). „A new model of cystic fibrosis pathology: lack of transport of glutathione and its thiocyanate conjugates”. Med. Hypotheses. 68 (1): 101—12. PMID 16934416. doi:10.1016/j.mehy.2006.06.020.
Prasad AB, Allard MW, Green ED (2008). „Confirming the phylogeny of mammals by use of large comparative sequence data sets”. Mol. Biol. Evol. 25 (9): 1795—808. PMC 2515873 . PMID 18453548. doi:10.1093/molbev/msn104.
Rowe SM, Miller S, Sorscher EJ (maj 2005). „Cystic fibrosis”. N. Engl. J. Med. 352 (19): 1992—2001. PMID 15888700. doi:10.1056/NEJMra043184.
Kavic, S. M.; Frehm, E. J.; Segal, A. S. (1999). „Case studies in cholera: Lessons in medical history and science”. The Yale journal of biology and medicine. 72 (6): 393—408. PMC 2579035 . PMID 11138935.
Araújo FG, Novaes FC, Santos NP, Martins VC, Souza SM, Santos SE, Ribeiro-dos-Santos AK (januar 2005). „Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil”. Braz. J. Med. Biol. Res. 38 (1): 11—5. PMID 15665983. doi:10.1590/S0100-879X2005000100003.
Sheppard DN, Welsh MJ (januar 1999). „Structure and function of the CFTR chloride channel”. Physiol. Rev. 79 (1 Suppl): S23—45. PMID 9922375.
Short DB, Trotter KW, Reczek D, Kreda SM, Bretscher A, Boucher RC, Stutts MJ, Milgram SL (jul 1998). „An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton”. J. Biol. Chem. 273 (31): 19797—801. PMID 9677412. doi:10.1074/jbc.273.31.19797.

sickkids.on.ca

genet.sickkids.on.ca

Cystic Fibrosis Mutation Database. „Genomic DNA sequence”. Архивирано из оригинала 22. 8. 2016. г. Приступљено 27. 8. 2016.

univ-montp2.fr

orthomam.univ-montp2.fr

„OrthoMaM phylogenetic marker: CFTR coding sequence”. Архивирано из оригинала 2. 3. 2016. г. Приступљено 27. 8. 2016.

web.archive.org

„OrthoMaM phylogenetic marker: CFTR coding sequence”. Архивирано из оригинала 2. 3. 2016. г. Приступљено 27. 8. 2016.
Cystic Fibrosis Mutation Database. „Genomic DNA sequence”. Архивирано из оригинала 22. 8. 2016. г. Приступљено 27. 8. 2016.