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Jessica R.C. Priestley
Jessica R.C. Priestley
Resident Physician, Children's Hospital of Philadelphia
Verified email at email.chop.edu
Title
Cited by
Cited by
Year
Serotonylation of vascular proteins important to contraction
SW Watts, JRC Priestley, JM Thompson
PLoS One 4 (5), e5682, 2009
1232009
The existence of a local 5‐hydroxytryptaminergic system in peripheral arteries
W Ni, TJ Geddes, JRC Priestley, T Szasz, DM Kuhn, SW Watts
British journal of pharmacology 154 (3), 663-674, 2008
852008
The NRF2 knockout rat: a new animal model to study endothelial dysfunction, oxidant stress, and microvascular rarefaction
JRC Priestley, KE Kautenburg, MC Casati, BT Endres, AM Geurts, ...
American Journal of Physiology-Heart and Circulatory Physiology 310 (4 …, 2016
722016
Mutation of Plekha7 attenuates salt-sensitive hypertension in the rat
BT Endres, JRC Priestley, O Palygin, MJ Flister, MJ Hoffman, ...
Proceedings of the National Academy of Sciences 111 (35), 12817-12822, 2014
662014
Mutation of SH2B3 (LNK), a Genome-Wide Association Study Candidate for Hypertension, Attenuates Dahl Salt-Sensitive Hypertension via Inflammatory Modulation
NP Rudemiller, H Lund, JRC Priestley, BT Endres, JW Prokop, HJ Jacob, ...
Hypertension 65 (5), 1111-1117, 2015
582015
The role of serotonin in haemostasis
D Duerschmied, C Bode
Hämostaseologie 29 (04), 356-359, 2009
432009
Reduced angiotensin II levels cause generalized vascular dysfunction via oxidant stress in hamster cheek pouch arterioles
JRC Priestley, MW Buelow, ST McEwen, BD Weinberg, M Delaney, ...
Microvascular research 89, 134-145, 2013
312013
Clinical spectrum of BCS1L Mitopathies and their underlying structural relationships
RA Baker, JRC Priestley, AM Wilstermann, KJ Reese, PR Mark
American Journal of Medical Genetics Part A 179 (3), 373-380, 2019
302019
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
SE Sheppard, ME March, C Seiler, LS Matsuoka, SE Kim, C Kao, AI Rubin, ...
JCI insight 8 (9), 2023
142023
Newborn screening for X-linked adrenoleukodystrophy: review of data and outcomes in Pennsylvania
JRC Priestley, LA Adang, S Drewes Williams, U Lichter-Konecki, ...
International Journal of Neonatal Screening 8 (2), 24, 2022
142022
NRF 2 activation with Protandim attenuates salt‐induced vascular dysfunction and microvascular rarefaction
JRC Priestley, KE Fink, JM McCord, JH Lombard
Microcirculation 26 (7), e12575, 2019
92019
Mutation of SH2B3 (LNK), a GWAS candidate for hypertension, attenuates Dahl SS hypertension via inflammatory modulation
NP Rudemiller, H Lund, JRC Priestley, BT Endres, JW Prokop, HJ Jacob, ...
Hypertension 65 (5), 1111, 2015
82015
Clinical effectiveness of telemedicine-based pediatric genetics care
KM Szigety, TB Crowley, KB Gaiser, EY Chen, JRC Priestley, LS Williams, ...
Pediatrics 150 (1), e2021054520, 2022
62022
The importance of succinylacetone: tyrosinemia type i presenting with hyperinsulinism and multiorgan failure following normal newborn screening
JRC Priestley, H Alharbi, KP Callahan, H Guzman, I Payan-Walters, ...
International journal of neonatal screening 6 (2), 39, 2020
62020
Vascular dysfunction precedes hypertension associated with a blood pressure locus on rat chromosome 12
SZ Prisco, JRC Priestley, BD Weinberg, AR Prisco, MJ Hoffman, HJ Jacob, ...
American Journal of Physiology-Heart and Circulatory Physiology 307 (8 …, 2014
52014
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
JRC Priestley, LM Pace, K Sen, A Aggarwal, CAPF Alves, IM Campbell, ...
Molecular Genetics and Metabolism Reports 33, 100931, 2022
42022
Mitochondrial hepatopathies
H Alharbi, JRC Priestley, BJ Wilkins, RD Ganetzky
Clinical Liver Disease 18 (5), 243-250, 2021
42021
Unmasking the challenges of Kabuki syndrome in adulthood: a case series
JRC Priestley, AL Rippert, C Condit, K Izumi, S Kallish, TG Drivas
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2023
32023
Urinary uracil: a useful marker for ornithine transcarbamylase deficiency in affected males
H Alsharhan, H Alharbi, J Priestley, R Ganetzky, M He
Clinical chemistry 66 (7), 988-989, 2020
32020
PhenoID, a language model normalizer of physical examinations from genetics clinical notes
D Weissenbacher, S Rawal, X Zhao, JRC Priestley, KM Szigety, ...
medRxiv, 2023.10. 16.23296894, 2023
12023
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