Ahmet Z Uluer
Overview
Explore the profile of Ahmet Z Uluer including associated specialties, affiliations and a list of published articles.
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11
Citations
453
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0
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Recent Articles
1.
Poret A, Schaefers M, Merakou C, Mansour K, Lagoudas G, Cross A, et al.
bioRxiv
. 2024 Feb;
PMID: 38370793
Bacteria evolving within human hosts encounter selective tradeoffs that render mutations adaptive in one context and deleterious in another. Here, we report that the cystic fibrosis-associated pathogen overcomes in-human selective...
2.
Singh H, Jani C, Marshall D, Franco R, Bhatt P, Podder S, et al.
Sci Rep
. 2023 Sep;
13(1):15030.
PMID: 37699961
Cystic fibrosis transmembrane conductance regulator modulators have revolutionized cystic fibrosis (CF) care in the past decade. This study explores the CF-related mortality trends in the US from 1999 to 2020....
3.
Uluer A, MacGregor G, Azevedo P, Indihar V, Keating C, Mall M, et al.
Lancet Respir Med
. 2023 Feb;
11(6):550-562.
PMID: 36842446
Background: Elexacaftor-tezacaftor-ivacaftor has been shown to be safe and efficacious in people with cystic fibrosis and at least one F508del allele. Our aim was to identify a novel cystic fibrosis...
4.
Robinson P, Jayasuriya G, Haggie S, Uluer A, Gaffin J, Fleming L
Paediatr Respir Rev
. 2021 Oct;
41:30-39.
PMID: 34686436
Asthma is among the most common medical conditions affecting children and young people, with adolescence a recognised period of increased risk, overrepresented in analyses examining recent increasing asthma mortality rates....
5.
Wu F, Opotowsky A, Denhoff E, Gongwer R, Gurvitz M, Landzberg M, et al.
Semin Thorac Cardiovasc Surg
. 2018 Aug;
30(4):462-469.
PMID: 30063966
While the Fontan procedure has improved life expectancy, patients with single ventricle physiology have impaired exercise capacity due to limited increase in pulmonary blood flow during activity. Enhancing the "thoracic...
6.
Nie S, Zhang H, Mayer K, Oppenheim F, Little F, Greenberg J, et al.
PLoS One
. 2015 Aug;
10(8):e0135237.
PMID: 26258476
Rationale: Monitoring clinical disease status in cystic fibrosis frequently requires invasive collection of clinical samples. Due to its noninvasive collection process and direct anatomic relationship with the lower airway, saliva...
7.
Nie S, Henley W, Miller S, Zhang H, Mayer K, Dennis P, et al.
Lab Chip
. 2014 Jan;
14(6):1087-98.
PMID: 24448498
During the last decade, saliva has emerged as a potentially ideal diagnostic biofluid for noninvasive testing. In this paper, we present an automated, integrated platform useable by minimally trained personnel...
8.
Uluer A, Waltz D, Kalish L, Adams S, Gerard C, Ericson D
J Cyst Fibros
. 2012 Oct;
12(1):54-9.
PMID: 23046902
Background: Burkholderia dolosa can result in chronic airway infection and rapid decline in lung function in patients with cystic fibrosis (CF). Amiloride has antibacterial properties that may be synergistic with...
9.
Accurso F, Rowe S, Clancy J, Boyle M, Dunitz J, Durie P, et al.
N Engl J Med
. 2010 Nov;
363(21):1991-2003.
PMID: 21083385
Background: A new approach in the treatment of cystic fibrosis involves improving the function of mutant cystic fibrosis transmembrane conductance regulator (CFTR). VX-770, a CFTR potentiator, has been shown to...
10.
Legere 3rd H, Palis R, Bouza T, Uluer A, Castells M
J Cyst Fibros
. 2009 Sep;
8(6):418-24.
PMID: 19740711
Background: CF patients often demonstrate hypersensitivity to one or multiple antibiotics due to frequent and repeated exposures. Attempts at antibiotic desensitization in this population are historically complicated by higher reaction...