Daphne B Mitchell
Overview
Explore the profile of Daphne B Mitchell including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
529
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Recent Articles
1.
Liu Q, Zhou Y, Cogan J, Mitchell D, Sheng Q, Zhao S, et al.
Am J Respir Crit Care Med
. 2023 Jan;
207(10):1345-1357.
PMID: 36622818
Up to 20% of idiopathic interstitial lung disease is familial, referred to as familial pulmonary fibrosis (FPF). An integrated analysis of FPF genetic risk was performed by comprehensively evaluating for...
2.
Salisbury M, Markin C, Wu P, Cogan J, Mitchell D, Liu Q, et al.
Am J Respir Crit Care Med
. 2022 Aug;
207(2):208-211.
PMID: 36036734
No abstract available.
3.
Salisbury M, Hewlett J, Ding G, Markin C, Douglas K, Mason W, et al.
Am J Respir Crit Care Med
. 2020 Feb;
201(10):1230-1239.
PMID: 32011901
The preclinical natural history of progressive lung fibrosis is poorly understood. Our goals were to identify risk factors for interstitial lung abnormalities (ILA) on high-resolution computed tomography (HRCT) scans and...
4.
Kropski J, Young L, Cogan J, Mitchell D, Lancaster L, Worrell J, et al.
Am J Respir Crit Care Med
. 2016 Oct;
195(11):1423-1428.
PMID: 27786550
No abstract available.
5.
Ma L, Shaver C, Grove B, Mitchell D, Wickersham N, Carnahan R, et al.
Clin Transl Med
. 2015 Jul;
4(1):63.
PMID: 26154059
Background: Activation of coagulation by expression of tissue factor (TF) in the airspace is a hallmark of acute lung injury (ALI) but the timing of TF activation in relationship to...
6.
Cogan J, Kropski J, Zhao M, Mitchell D, Rives L, Markin C, et al.
Am J Respir Crit Care Med
. 2015 Jan;
191(6):646-55.
PMID: 25607374
Rationale: Up to 20% of cases of idiopathic interstitial pneumonia cluster in families, comprising the syndrome of familial interstitial pneumonia (FIP); however, the genetic basis of FIP remains uncertain in...
7.
Kropski J, Pritchett J, Zoz D, Crossno P, Markin C, Garnett E, et al.
Am J Respir Crit Care Med
. 2014 Nov;
191(4):417-26.
PMID: 25389906
Rationale: Asymptomatic relatives of patients with familial interstitial pneumonia (FIP), the inherited form of idiopathic interstitial pneumonia, carry increased risk for developing interstitial lung disease. Objectives: Studying these at-risk individuals...
8.
Kropski J, Mitchell D, Markin C, Polosukhin V, Choi L, Johnson J, et al.
Chest
. 2014 Feb;
146(1):e1-e7.
PMID: 24504062
Short telomeres are frequently identified in patients with idiopathic pulmonary fibrosis (IPF) and its inherited form, familial interstitial pneumonia (FIP). We identified a kindred with FIP with short telomeres who...
9.
Degryse A, Xu X, Newman J, Mitchell D, Tanjore H, Polosukhin V, et al.
Exp Lung Res
. 2012 Mar;
38(3):124-34.
PMID: 22394286
Idiopathic pulmonary fibrosis (IPF) is characterized by interstitial lung infiltrates, dyspnea, and progressive respiratory failure. Reports linking telomerase mutations to familial interstitial pneumonia (FIP) suggest that telomerase activity and telomere...
10.
Bastarache J, Koyama T, Wickersham N, Mitchell D, Mernaugh R, Ware L
J Immunol Methods
. 2011 Feb;
367(1-2):33-9.
PMID: 21277854
Background: Multiplex immunoassays offer many advantages over singleplex assays for the analysis of multiple analytes in a single sample. We sought to validate a specific multiplex cytokine immunoassay (Human 9-plex...