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cystic fibrosis gen.
cystic fibrosis gene.
Ultimo aggiornamento 2014-11-28
Frequenza di utilizzo: 2
Qualità:
cystic fibrosis (2004)
cystic fibrosis (2005)
Ultimo aggiornamento 2018-02-13
Frequenza di utilizzo: 1
Qualità:
what is cystic fibrosis?
what is cystic fibrosis?
Ultimo aggiornamento 2018-02-13
Frequenza di utilizzo: 1
Qualità:
zystenauge [cystic eyeball]
cystic eyeball
Ultimo aggiornamento 2014-12-09
Frequenza di utilizzo: 5
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Attenzione: Questo allineamento potrebbe essere errato.
Eliminalo se ritieni che sia così.
treatment of cystic fibrosis
treatment of cystic fibrosis
Ultimo aggiornamento 2011-10-23
Frequenza di utilizzo: 5
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Attenzione: Questo allineamento potrebbe essere errato.
Eliminalo se ritieni che sia così.
cystic fibrosis (cf) (2008)
cystic fibrosis (cf) (2008)
Ultimo aggiornamento 2018-02-13
Frequenza di utilizzo: 1
Qualità:
quality of life in cystic fibrosis.
association of clinical variables in children with cystic fibrosis and health-related quality of life.
Ultimo aggiornamento 2018-02-13
Frequenza di utilizzo: 1
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prevention of pseudomonas aeruginosa infections in patients with cystic fibrosis
prevention of pseudomonas aeruginosa infections in patients with cystic fibrosis
die entwicklung wurde von der amerikanischen "cystic fibrosis foundation" gefördert.
denufosol (inn) is an inhaled drug for the treatment of cystic fibrosis, being developed by inspire pharmaceuticals and sponsored by the cystic fibrosis foundation.
treatment of pseudomonas aeruginosa lung infection (including colonisation) in cystic fibrosis
• treatment of pseudomonas aeruginosa lung infection
an in vitro study of the susceptibility of mobile and cystic forms of borrelia burgdorferi to metronidazole.
an in vitro study of the susceptibility of mobile and cystic forms of borrelia burgdorferi to metronidazole.
association of clinical variables in children with cystic fibrosis and health-related quality of life.
association of clinical variables in children with cystic fibrosis and health-related quality of life.
ivacaftor wurde mit finanzieller unterstützung der us-amerikanischen patientenorganisation "cystic fibrosis foundation" entwickelt.
in 1959, the median age of survival of children with cystic fibrosis in the united states was six months.
verfahren zum nachweis von erkrankungen, die auf defekten des proteins cystic fibrosis transmembrane conductance regulator (cftr) beruhen
method for detecting diseases that are associated with defects of cystic fibrosis transmembrane conductance regulator (cftr) protein
the occurrence of cystic forms of borrelia burgdorferi in vitro was noted, and these cysts were able to be transformed to normal, mobile spirochetes.
the occurrence of cystic forms of borrelia burgdorferi in vitro was noted, and these cysts were able to be transformed to normal, mobile spirochetes.
das "cftr"-gen codiert für das protein "cystic fibrosis transmembrane conductance regulator" (cftr).
the product of this gene (the cftr) is a chloride ion channel important in creating sweat, digestive juices and mucus.
