Lisa Rice
Overview
Explore the profile of Lisa Rice including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
14
Citations
137
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0
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Recent Articles
1.
Rice L
Vet Rec
. 2024 May;
194(11):i-ii.
PMID: 38819847
Lisa Rice is south area supervisor for Pet Blood Bank, having first gained experience in small animal practice then training to take blood donations and organise donation sessions when she...
2.
Baek R, Coughlan K, Jiang L, Liang M, Ci L, Singh H, et al.
Nat Commun
. 2024 May;
15(1):3804.
PMID: 38714648
Messenger RNA (mRNA) therapeutics delivered via lipid nanoparticles hold the potential to treat metabolic diseases caused by protein deficiency, including propionic acidemia (PA), methylmalonic acidemia (MMA), and phenylketonuria (PKU). Herein...
3.
Perocheau D, Gurung S, Touramanidou L, Duff C, Sharma G, Sebire N, et al.
F1000Res
. 2024 Apr;
12:1580.
PMID: 38618017
Background: In academic research and the pharmaceutical industry, cell lines and animal models are considered as gold standards in modelling diseases and assessing therapeutic efficacy. However, both models have intrinsic...
4.
Gurung S, Timmermand O, Perocheau D, Gil-Martinez A, Minnion M, Touramanidou L, et al.
Sci Transl Med
. 2024 Jan;
16(729):eadh1334.
PMID: 38198573
The urea cycle enzyme argininosuccinate lyase (ASL) enables the clearance of neurotoxic ammonia and the biosynthesis of arginine. Patients with ASL deficiency present with argininosuccinic aciduria, an inherited metabolic disease...
5.
Gurung S, Karamched S, Perocheau D, Seunarine K, Baldwin T, Alrashidi H, et al.
J Inherit Metab Dis
. 2023 Dec;
47(6):1213-1227.
PMID: 38044746
Argininosuccinate lyase (ASL) is integral to the urea cycle detoxifying neurotoxic ammonia and the nitric oxide (NO) biosynthesis cycle. Inherited ASL deficiency causes argininosuccinic aciduria (ASA), a rare disease with...
6.
Sanges S, Rice L, Tu L, Valenzi E, Cracowski J, Montani D, et al.
Ann Rheum Dis
. 2023 Jan;
82(3):365-373.
PMID: 36600187
Objectives: To mine the serum proteome of patients with systemic sclerosis-associated pulmonary arterial hypertension (SSc-PAH) and to detect biomarkers that may assist in earlier and more effective diagnosis and treatment....
7.
Cao J, Choi M, Guadagnin E, Soty M, Silva M, Verzieux V, et al.
Nat Commun
. 2021 May;
12(1):3090.
PMID: 34035281
Glycogen Storage Disease 1a (GSD1a) is a rare, inherited metabolic disorder caused by deficiency of glucose 6-phosphatase (G6Pase-α). G6Pase-α is critical for maintaining interprandial euglycemia. GSD1a patients exhibit life-threatening hypoglycemia...
8.
Schulman-Marcus J, Mookherjee S, Rice L, Lyubarova R
Am J Med
. 2019 Feb;
132(7):781-782.
PMID: 30738728
No abstract available.
9.
Moll M, Christmann R, Zhang Y, Whitfield M, Wang Y, Rice L, et al.
J Scleroderma Relat Disord
. 2018 Dec;
3(3):242-248.
PMID: 30498788
Objective: Pulmonary arterial hypertension (PAH) and interstitial lung disease (ILD) are major causes of mortality in systemic sclerosis (SSc). We used a previously identified microarray biomarker to determine if SSc-PAH...
10.
CpGB DNA activates dermal macrophages and specifically recruits inflammatory monocytes into the skin
Mathes A, Rice L, Affandi A, DiMarzio M, Rifkin I, Stifano G, et al.
Exp Dermatol
. 2014 Nov;
24(2):133-9.
PMID: 25425469
Toll-like receptor 9 (TLR9) drives innate immune responses after recognition of foreign or endogenous DNA containing unmethylated CpG motifs. DNA-mediated TLR9 activation is highly implicated in the pathogenesis of several...