A Novel Angiotensin-Converting Enzyme–Related Carboxypeptidase (ACE2) Converts Angiotensin I to Angiotensin 1-9
By M. Donoghue, F. Hsieh, E. Baronas, Kevin Godbout, Michael L. Gosselin, N. Stagliano, M. Donovan, Betty Woolf, K. Robison, R. Jeyaseelan and 2 more. Circulation Research, 2000
2,919 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/68d83a261254685e92c4d6959cb2b71ac40610a1
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In Cardiology and Cardiovascular Medicine
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Citations in the corpus
- Angiotensin-Converting Enzyme 2: SARS-CoV-2 Receptor and Regulator of the Renin-Angiotensin System (2020, background): “Angiotensin-(1-7) inhibits growth of cardiac myocytes through activation of the mas receptor.”
- Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus (2003, background): “Here we identify a metallopeptidase, angiotensin-converting enzyme 2 (ACE2”
- Angiotensin-converting enzyme 2 is an essential regulator of heart function (2002, background): “Recently, a homologue of ACE, termed ACE2, has been identified; it is predominantly expressed in the vascular endothelial cells of the kidney and hear”
- Role of the ACE2/Angiotensin 1–7 axis of the Renin-Angiotensin System in Heart Failure (2016, methodology): “teinase catalytic domains of ACE2 and ACE are 42% identical according to the findings of Donoghue et al.(32) In spite of such”
- The pivotal link between ACE2 deficiency and SARS-CoV-2 infection (2020, positive): “[2,3] The ACE2 receptor, discovered by two independent groups in year 2000, [4,5] is a trans-membrane type I glycoprotein (mono-carboxypeptidase) composed by 805 amino acids which uses a single extracellular catalytic domain to remove one single amino acid from the octapeptide angiotensin II to gene”
- ACE2 Receptor Expression and Severe Acute Respiratory Syndrome Coronavirus Infection Depend on Differentiation of Human Airway Epithelia (2005, background): “sue, and epithelia of the small intestine and testes (6, 10, 11).”
- In silico SARS-CoV-2 vaccine development for Omicron strain using reverse vaccinology (2022, methodology): “In the final step we performed molecular docking of the vaccine candidate with human ACE2 (Donoghue et al. 2000).”