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Loss of CD4+ T cell-intrinsic arginase 1 accelerates Th1 response kinetics and reduces lung pathology during influenza infection
Loss of CD4+ T cell-intrinsic arginase 1 accelerates Th1 response kinetics and reduces lung pathology during influenza infection
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Loss of CD4+ T cell-intrinsic arginase 1 accelerates Th1 response kinetics and reduces lung pathology during influenza infection

West, Erin E. ; Merle, Nicolas S. ; Kamiński, Marcin M. ; Palacios, Gustavo ; Kumar, Dhaneshwar ; Wang, Luopin ; Bibby, Jack A. ; Overdahl, Kirsten ; Jarmusch, Alan K. ; Freeley, Simon ; Lee, Duck-Yeon ; Thompson, J. Will ; Yu, Zu-Xi ; Taylor, Naomi ; Sitbon, Marc ; Green, Douglas R. ; Bohrer, Andrea ; Mayer-Barber, Katrin D. ; Afzali, Behdad ; Kazemian, Majid ; Scholl-Buergi, Sabine ; Karall, Daniela ; Huemer, Martina ; Kemper, Claudia

Immunity (Cambridge, Mass.), 2023-09, Vol.56 (9), p.2036-2053.e12 [Peer Reviewed Journal]

United States: Elsevier Inc

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2
Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency
Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency
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Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency

Diaz, George A. ; Schulze, Andreas ; McNutt, Markey C. ; Leão‐Teles, Elisa ; Merritt, J. Lawrence ; Enns, Gregory M. ; Batzios, Spyros ; Bannick, Allison ; Zori, Roberto T. ; Sloan, Leslie S. ; Potts, Susan L. ; Bubb, Gillian ; Quinn, Anthony G.

Journal of inherited metabolic disease, 2021-07, Vol.44 (4), p.847-856 [Peer Reviewed Journal]

Hoboken, USA: John Wiley & Sons, Inc

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3
Mutations and common variants in the human arginase 1 (ARG1) gene: Impact on patients, diagnostics, and protein structure considerations
Mutations and common variants in the human arginase 1 (ARG1) gene: Impact on patients, diagnostics, and protein structure considerations
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Mutations and common variants in the human arginase 1 (ARG1) gene: Impact on patients, diagnostics, and protein structure considerations

Diez‐Fernandez, Carmen ; Rüfenacht, Véronique ; Gemperle, Corinne ; Fingerhut, Ralph ; Häberle, Johannes

Human mutation, 2018-08, Vol.39 (8), p.1029-1050 [Peer Reviewed Journal]

United States: Hindawi Limited

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4
Newborn screening for hyperargininemia due to arginase 1 deficiency
Newborn screening for hyperargininemia due to arginase 1 deficiency
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Newborn screening for hyperargininemia due to arginase 1 deficiency

Therrell, Bradford L. ; Currier, Robert ; Lapidus, David ; Grimm, Meredith ; Cederbaum, Stephen D.

Molecular genetics and metabolism, 2017-08, Vol.121 (4), p.308-313 [Peer Reviewed Journal]

United States: Elsevier Inc

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5
Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia
Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia
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Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia

Dorum, Sevil ; Havalı, Cengiz

Pediatrics international, 2022-01, Vol.64 (1), p.e14945-n/a [Peer Reviewed Journal]

Australia: Blackwell Publishing Ltd

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6
Health care resource utilization in the management of patients with Arginase 1 Deficiency in the US: a retrospective, observational, claims database study
Health care resource utilization in the management of patients with Arginase 1 Deficiency in the US: a retrospective, observational, claims database study
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Health care resource utilization in the management of patients with Arginase 1 Deficiency in the US: a retrospective, observational, claims database study

Bin Sawad, Aseel ; Jackimiec, John ; Bechter, Mark ; Hull, Michael ; Yeaw, Jason ; Wang, Yi ; Diaz, George A.

Journal of medical economics, 2022-12, Vol.25 (1), p.848-856 [Peer Reviewed Journal]

Taylor & Francis

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7
Current status of surviving patients with arginase 1 deficiency in Japan
Current status of surviving patients with arginase 1 deficiency in Japan
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Current status of surviving patients with arginase 1 deficiency in Japan

Kido, Jun ; Matsumoto, Shirou ; Takeshita, Eiko ; Hayakawa, Chiemi ; Yamada, Keitaro ; Kagawa, Jiro ; Nakajima, Yoko ; Ito, Tetsuya ; Iijima, Hiroyuki ; Endo, Fumio ; Nakamura, Kimitoshi

Molecular genetics and metabolism reports, 2021-12, Vol.29, p.100805-100805, Article 100805 [Peer Reviewed Journal]

Elsevier Inc

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8
A new metabolic disorder in human cationic amino acid transporter‐2 that mimics arginase 1 deficiency in newborn screening
A new metabolic disorder in human cationic amino acid transporter‐2 that mimics arginase 1 deficiency in newborn screening
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A new metabolic disorder in human cationic amino acid transporter‐2 that mimics arginase 1 deficiency in newborn screening

Yahyaoui, Raquel ; Blasco‐Alonso, Javier ; Benito, Carmen ; Rodríguez‐García, Enrique ; Andrade, Fernando ; Aldámiz‐Echevarría, Luis ; Muñoz‐Hernández, María C. ; Vega, Ana I. ; Pérez‐Cerdá, Celia ; García‐Martín, María L. ; Pérez, Belén

Journal of inherited metabolic disease, 2019-05, Vol.42 (3), p.407-413 [Peer Reviewed Journal]

Hoboken, USA: John Wiley & Sons, Inc

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9
Hyperargininemia Due to Arginase 1 Deficiency: Variability in Clinical and Biochemical Presentations in Malaysian children
Hyperargininemia Due to Arginase 1 Deficiency: Variability in Clinical and Biochemical Presentations in Malaysian children
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Hyperargininemia Due to Arginase 1 Deficiency: Variability in Clinical and Biochemical Presentations in Malaysian children

Habib, Anasufiza ; Mohamed Shakrin, Norashareena

Clinical pathology (Thousand Oaks, Ventura County, Calif.), 2022-04, Vol.15, p.2632010X221093274-2632010X221093274 [Peer Reviewed Journal]

London, England: SAGE Publications

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10
Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice
Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice
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Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice

Chennupati, Ramesh ; Meens, Merlijn J. ; Janssen, Ben J. ; Dijk, Paul ; Hakvoort, Theodorus B. M. ; Lamers, Wouter H. ; De Mey, Jo G. R. ; Koehler, S. Eleonore

Physiological reports, 2018-06, Vol.6 (11), p.e13717-n/a [Peer Reviewed Journal]

United States: John Wiley & Sons, Inc

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