[Detection of mutations of the HNF1B gene in children with congenital anomalies of the kidney and urinary tract]

Autor: M Nicole, Bascur P, M Luisa, Ceballos O, Mauricio, Farfán U, Iván, Gajardo H, Joaquín, López C

Publikováno v: Revista chilena de pediatria. 89(6)

Congenital anomalies of the kidney and urinary tract are caused by genetic alterations mostly unknown. Mutations in the gene that codes for hepatocyte nuclear factor 1B (HNF1B) are the most frequently described monogenic causes. Data are unknown in C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::12ca0373c0bee9ef12794b4e85df5f90
https://pubmed.ncbi.nlm.nih.gov/30725063

Caracterización molecular de mecanismos de resistencia a cloranfenicol en cepas de Shigella flexneri aisladas en niños chilenos con diarrea aguda

Autor: Oscar Flores G, Guido Mora L, Cecilia Toro U, Mauricio Farfán U, Niurka Navarro G, Valeria Prado J

Publikováno v: Revista médica de Chile, Volume: 130, Issue: 3, Pages: 275-280, Published: MAR 2002
Revista médica de Chile v.130 n.3 2002
SciELO Chile
CONICYT Chile
instacron:CONICYT

Background: Chloramphenicol is one of the therapeutic options for shigellosis, but resistance to this antimicrobial is increasing. Aim: To characterize molecular mechanisms conferring resistance to chloramphenicol (CmR) in Shigella flexneri strains i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::256eda0745a7a723cead77f04bdeedd8
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000300005&lng=en&tlng=en

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