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The Journal of Clinical Investigation|August 15, 2017
Prolyl hydroxylase 2 inactivation enhances glycogen storage and promotes excessive neutrophilic responsesPranvera Sadiku, Joseph A Willson, Rebecca S Dickinson, et al.
American Journal of Respiratory and Critical Care Medicine|February 1, 2023
NRF2 Activation Reprograms Defects in Oxidative Metabolism to Restore Macrophage Function in Chronic Obstructive Pulmonary DiseaseEilise M Ryan, Pranvera Sadiku, Patricia Coelho, et al.
Neurology|January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.
The European Respiratory Journal|July 30, 2016
High attenuation areas on chest computed tomography in community-dwelling adults: the MESA studyAnna J Podolanczuk, Elizabeth C Oelsner, R Graham Barr, et al.
Wellcome Open Research|May 28, 2021
-------A type I IFN, prothrombotic hyperinflammatory neutrophil signature is distinct for COVID-19 ARDS--Leila Reyes, Manuel A Sanchez-Garcia, Tyler Morrison, et al.
Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Iscience|February 28, 2022
Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19Jun Wang, Prasanti Kotagiri, Paul A Lyons, et al.
Nature Immunology|May 23, 2017
BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiencyBehdad Afzali, Juha Grönholm, Jana Vandrovcova, et al.
Neurology|December 14, 2005
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD StudyS Karamohamed, J C Latourelle, B A Racette, et al.
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