Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients. (Q34684122)

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English	Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients.	scientific article

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29 February 2020

Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients (English)

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29 February 2020

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cystic fibrosis

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transmembrane protein

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1

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29 February 2020

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29 February 2020

Marco Lucarelli

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29 February 2020

Floriana Santangelo

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29 February 2020

Antonella Gagliardi

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29 February 2020

Riccardo Valerio De Biase

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29 February 2020

Serena Quattrucci

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29 February 2020

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Antonella Stamato

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29 February 2020

Serenella Bertasi

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29 February 2020

Maria Pia Conte

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29 February 2020

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17 April 2013

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29 February 2020

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29 February 2020

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29 February 2020

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29 February 2020

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29 February 2020

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17 April 2013

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Update of faecal markers of inflammation in children with cystic fibrosis.

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Direct sampling of cystic fibrosis lungs indicates that DNA-based analyses of upper-airway specimens can misrepresent lung microbiota

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Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients

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A pathobiont of the microbiota balances host colonization and intestinal inflammation.

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Commensal bacteria, traditional and opportunistic pathogens, dysbiosis and bacterial killing in inflammatory bowel diseases

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Predominant role of host genetics in controlling the composition of gut microbiota

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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

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Risk factors for small bowel bacterial overgrowth in cystic fibrosis

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A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene

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based on heuristic

inferred from PubMed ID database lookup

Interobserver variance in clinical scoring for cystic fibrosis

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro inhibition activity of nisin A, nisin Z, pediocin PA-1 and antibiotics against common intestinal bacteria

1 reference

https://pubmed.ncbi.nlm.nih.gov/23613805

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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29 February 2020

2013PLoSO...861176S

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29 February 2020

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29 February 2020

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