Hemo (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hemo" in Spanish language version.

refsWebsite

Global rank Spanish rank

17nih.gov

4^th place

6doi.org

2^nd place

1web.archive.org

1^st place

1americanscientist.org

7,231^st place

5,615^th place

1umassmed.edu

low place

1issn.org

57^th place

3^rd place

1portlandpress.com

low place

1wiley.com

222^nd place

135^th place

americanscientist.org

Hardison, R. (1999). «The Evolution of Hemoglobin: Studies of a very ancient protein suggest that changes in gene regulation are an important part of the evolutionary story». American Scientist 87 (2): 126. Archivado desde el original el 10 de abril de 2016.

doi.org

dx.doi.org

Brown, K. R.; Brown, B. M.; Hoagland, E.; Mayne, C. L.; Hegg, E. L. (2004). «Heme A Synthase Does Not Incorporate Molecular Oxygen into the Formyl Group of Heme A». Biochemistry 43 (27): 8616-8624. PMID 15236569. doi:10.1021/bi049056m.
Kolluri, Sridevi (17 de marzo de 2004). Upregulation of Heme Pathway Enzyme ALA Synthase-1 by Glutethimide and 4,6-Dioxoheptanoic Acid and Downregulation by Glucose and Heme: A Dissertation (en inglés estadounidense). doi:10.13028/yyrz-qa79. Consultado el 26 de febrero de 2023.
Pamplona, A.; Ferreira, A.; Balla, J.; Jeney, V.; Balla, G.; Epiphanio, S.; Chora, A.; Rodrigues, C. D. et al. (June 2007). «Heme oxygenase-1 and carbon monoxide suppress the pathogenesis of experimental cerebral malaria.». Nature Medicine 13 (6): 703-710. PMID 17496899. doi:10.1038/nm1586.
Larsen, Rasmus; Gozzelino, Raffaella; Jeney, Viktória; Tokaji, László; Bozza, Fernando A.; Japiassú, André M.; Bonaparte, Dolores; Cavalcante, Moisés Marinho; Chora, Angelo; Ferreira, Ana; Marguti, Ivo; Cardoso, Sílvia; Sepúlveda, Nuno; Smith, Ann; Soares, Miguel P. (29 de septiembre de 2010). «A central role for free heme in the pathogenesis of severe sepsis». Science Translational Medicine 2 (51): 51ra71. ISSN 1946-6242. PMID 20881280. doi:10.1126/scitranslmed.3001118. Consultado el 8 de agosto de 2016.
Bustad, HJ; Vorland, M; Ronneseth, E; Sandberg, S; Martinez, A; Toska, K (8 de agosto de 2013). «Conformational stability and activity analysis of two hydroxymethylbilane synthase mutants, K132N and V215E, with different phenotypic association with acute intermittent porphyria». Bioscience Reports 33 (4). doi:10.1042/BSR20130045. Consultado el 18 de noviembre de 2014.
Badenas, C; To-Figueras, J; Phillips, JD; Warby, CA; Munoz, C; Herrero, C (Abril de 2009). «Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives». Clinical Genetics 75 (4): 346-353. PMC 3804340. PMID 19419417. doi:10.1111/j.1399-0004.2009.01153.x. Consultado el 18 de noviembre de 2014.

issn.org

portal.issn.org

Larsen, Rasmus; Gozzelino, Raffaella; Jeney, Viktória; Tokaji, László; Bozza, Fernando A.; Japiassú, André M.; Bonaparte, Dolores; Cavalcante, Moisés Marinho; Chora, Angelo; Ferreira, Ana; Marguti, Ivo; Cardoso, Sílvia; Sepúlveda, Nuno; Smith, Ann; Soares, Miguel P. (29 de septiembre de 2010). «A central role for free heme in the pathogenesis of severe sepsis». Science Translational Medicine 2 (51): 51ra71. ISSN 1946-6242. PMID 20881280. doi:10.1126/scitranslmed.3001118. Consultado el 8 de agosto de 2016.

nih.gov

ncbi.nlm.nih.gov

Caughey, W. S.; Smythe, G. A.; O'Keeffe, D. H.; Maskasky, J. E.; Smith, M. I. (1975). «Heme A of cytochrome c oxicase. Structure and properties: comparisons with hemes B, C, and S and derivatives». J. Biol. Chem. 250 (19): 7602-7622. PMID 170266.
Brown, K. R.; Brown, B. M.; Hoagland, E.; Mayne, C. L.; Hegg, E. L. (2004). «Heme A Synthase Does Not Incorporate Molecular Oxygen into the Formyl Group of Heme A». Biochemistry 43 (27): 8616-8624. PMID 15236569. doi:10.1021/bi049056m.
Rae, T. D.; Goff, H. M. (1998). «The heme prosthetic group of lactoperoxidase. Structural characteristics of heme l and heme l-peptides». J. Biol. Chem. 273 (43): 27968-77. PMID 9774411.
Murshudov, G. N.; Grebenko, A. I.; Barynin, V.; Dauter, Z.; Wilson, K. S.; Vainshtein, B. K.; Melik-Adamyan, W; Bravo, J. et al. (1996). «Structure of the heme d of Penicillium vitale and Escherichia coli catalases». J. Biol. Chem. 271 (15): 8863-8. PMID 8621527.
Bunn, H. F.; Jandl, J. H. (1966). «Exchange of heme among hemoglobin molecules.». Proc Natl Acad Sci U S A 56 (3): 974-8. PMID 5230192.
Smith, M. L.; Paul, J.; Ohlsson, P. I.; Hjortsberg, K.; Paul, K. G. (1991). «Heme-protein fission under nondenaturing conditions». Proc Natl Acad Sci U S A 88 (3): 882-6. PMID 1846966.
Pamplona, A.; Ferreira, A.; Balla, J.; Jeney, V.; Balla, G.; Epiphanio, S.; Chora, A.; Rodrigues, C. D. et al. (June 2007). «Heme oxygenase-1 and carbon monoxide suppress the pathogenesis of experimental cerebral malaria.». Nature Medicine 13 (6): 703-710. PMID 17496899. doi:10.1038/nm1586.
Larsen, Rasmus; Gozzelino, Raffaella; Jeney, Viktória; Tokaji, László; Bozza, Fernando A.; Japiassú, André M.; Bonaparte, Dolores; Cavalcante, Moisés Marinho; Chora, Angelo; Ferreira, Ana; Marguti, Ivo; Cardoso, Sílvia; Sepúlveda, Nuno; Smith, Ann; Soares, Miguel P. (29 de septiembre de 2010). «A central role for free heme in the pathogenesis of severe sepsis». Science Translational Medicine 2 (51): 51ra71. ISSN 1946-6242. PMID 20881280. doi:10.1126/scitranslmed.3001118. Consultado el 8 de agosto de 2016.
Plewinska, Magdalena; Thunell, Stig; Holmberg, Lars; Wetmur, James; Desnick, Robert (1991). «delta-Aminolevulinate dehydratase deficient porphyria: identification of the molecular lesions in a severely affected homozygote». American Journal of Human Genetics (49): 167-174. PMC 1683193. PMID 2063868. Consultado el 18 de noviembre de 2014.
Aurizi, C; Lupia Palmieri, G; Barbieri, L; Macri, A; Sorge, F; Usai, G; Biolcati, G (February 2009). «Four novel mutations of the coproporphyrinogen III oxidase gene». Cellular and Molecular Biology 55 (1): 8-15. PMID 19267996. Consultado el 18 de noviembre de 2014.
Martinez di Montemuros, F; Di Pierro, E; Patti, E; Tavazzi, D; Danielli, MG; Biolcati, G; Rocchi, E; Cappllini, MD (Diciembre de 2002). «Molecular characterization of porphyrias in Italy: a diagnostic flow-chart». Cellular and Molecular Biology 48 (8): 867-876. PMID 12699245. Consultado el 18 de noviembre de 2014.
Badenas, C; To-Figueras, J; Phillips, JD; Warby, CA; Munoz, C; Herrero, C (Abril de 2009). «Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives». Clinical Genetics 75 (4): 346-353. PMC 3804340. PMID 19419417. doi:10.1111/j.1399-0004.2009.01153.x. Consultado el 18 de noviembre de 2014.

pubmed.ncbi.nlm.nih.gov

Caughey, W. S.; Smythe, G. A.; O'Keeffe, D. H.; Maskasky, J. E.; Smith, M. I. (1975). «Heme A of cytochrome c oxicase. Structure and properties: comparisons with hemes B, C, and S and derivatives». J. Biol. Chem. 250 (19): 7602-7622. PMID 170266.
Brown, K. R.; Brown, B. M.; Hoagland, E.; Mayne, C. L.; Hegg, E. L. (2004). «Heme A Synthase Does Not Incorporate Molecular Oxygen into the Formyl Group of Heme A». Biochemistry 43 (27): 8616-8624. PMID 15236569. doi:10.1021/bi049056m.
Plewinska, Magdalena; Thunell, Stig; Holmberg, Lars; Wetmur, James; Desnick, Robert (1991). «delta-Aminolevulinate dehydratase deficient porphyria: identification of the molecular lesions in a severely affected homozygote». American Journal of Human Genetics (49): 167-174. PMC 1683193. PMID 2063868. Consultado el 18 de noviembre de 2014.
Aurizi, C; Lupia Palmieri, G; Barbieri, L; Macri, A; Sorge, F; Usai, G; Biolcati, G (February 2009). «Four novel mutations of the coproporphyrinogen III oxidase gene». Cellular and Molecular Biology 55 (1): 8-15. PMID 19267996. Consultado el 18 de noviembre de 2014.
Martinez di Montemuros, F; Di Pierro, E; Patti, E; Tavazzi, D; Danielli, MG; Biolcati, G; Rocchi, E; Cappllini, MD (Diciembre de 2002). «Molecular characterization of porphyrias in Italy: a diagnostic flow-chart». Cellular and Molecular Biology 48 (8): 867-876. PMID 12699245. Consultado el 18 de noviembre de 2014.

portlandpress.com

Bustad, HJ; Vorland, M; Ronneseth, E; Sandberg, S; Martinez, A; Toska, K (8 de agosto de 2013). «Conformational stability and activity analysis of two hydroxymethylbilane synthase mutants, K132N and V215E, with different phenotypic association with acute intermittent porphyria». Bioscience Reports 33 (4). doi:10.1042/BSR20130045. Consultado el 18 de noviembre de 2014.

umassmed.edu

repository.escholarship.umassmed.edu

Kolluri, Sridevi (17 de marzo de 2004). Upregulation of Heme Pathway Enzyme ALA Synthase-1 by Glutethimide and 4,6-Dioxoheptanoic Acid and Downregulation by Glucose and Heme: A Dissertation (en inglés estadounidense). doi:10.13028/yyrz-qa79. Consultado el 26 de febrero de 2023.

web.archive.org

Hardison, R. (1999). «The Evolution of Hemoglobin: Studies of a very ancient protein suggest that changes in gene regulation are an important part of the evolutionary story». American Scientist 87 (2): 126. Archivado desde el original el 10 de abril de 2016.

wiley.com

onlinelibrary.wiley.com

Badenas, C; To-Figueras, J; Phillips, JD; Warby, CA; Munoz, C; Herrero, C (Abril de 2009). «Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives». Clinical Genetics 75 (4): 346-353. PMC 3804340. PMID 19419417. doi:10.1111/j.1399-0004.2009.01153.x. Consultado el 18 de noviembre de 2014.