Pages that link to "Q301630"
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The following pages link to angiotensin I converting enzyme 2 (Q301630):
Displayed 50 items.
- SARSr-CoV (Q278567) (← links)
- ACE2 (Q14875321) (← links)
- (Q21104939) (redirect page) (← links)
- A human homolog of angiotensin-converting enzyme. Cloning and functional expression as a captopril-insensitive carboxypeptidase (Q22254730) (← links)
- A novel angiotensin-converting enzyme-related carboxypeptidase (ACE2) converts angiotensin I to angiotensin 1-9 (Q24290169) (← links)
- ACE2: from vasopeptidase to SARS virus receptor (Q24294404) (← links)
- Evaluation of angiotensin-converting enzyme (ACE), its homologue ACE2 and neprilysin in angiotensin peptide metabolism (Q24300310) (← links)
- Cloning and characterization of a secreted form of angiotensin-converting enzyme 2 (Q24304865) (← links)
- A transmembrane serine protease is linked to the severe acute respiratory syndrome coronavirus receptor and activates virus entry (Q24306622) (← links)
- Identification of residues in the receptor-binding domain (RBD) of the spike protein of human coronavirus NL63 that are critical for the RBD-ACE2 receptor interaction (Q24311580) (← links)
- Angiotensin-converting enzyme 2 overexpression in the subfornical organ prevents the angiotensin II-mediated pressor and drinking responses and is associated with angiotensin II type 1 receptor downregulation (Q24311938) (← links)
- Lipid rafts are involved in SARS-CoV entry into Vero E6 cells (Q24314417) (← links)
- Heart block, ventricular tachycardia, and sudden death in ACE2 transgenic mice with downregulated connexins (Q24321922) (← links)
- ACE2: a new target for cardiovascular disease therapeutics (Q24337633) (← links)
- TMPRSS2 and ADAM17 cleave ACE2 differentially and only proteolysis by TMPRSS2 augments entry driven by the severe acute respiratory syndrome coronavirus spike protein (Q24339582) (← links)
- The influence of Angiotensin converting enzyme and angiotensinogen gene polymorphisms on hypertrophic cardiomyopathy (Q27002339) (← links)
- Survivin and angiotensin-converting enzyme polymorphisms with risk of colorectal cancer: a systematic review and meta-analysis (Q27013718) (← links)
- Hydrolysis of biological peptides by human angiotensin-converting enzyme-related carboxypeptidase (Q28115041) (← links)
- Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor (Q30219701) (← links)
- Modulation of TNF-alpha-converting enzyme by the spike protein of SARS-CoV and ACE2 induces TNF-alpha production and facilitates viral entry (Q36693984) (← links)
- Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis. (Q40510688) (← links)
- HeLa-ACE2-TMPRSS2 Cells Are Useful for the Isolation of Human Coronavirus 229E. (Q40674745) (← links)
- Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations. (Q48727564) (← links)
- ACE2 hydrolyzes Angiotensin-(1-10) to Angiotensin-(1-9) (Q50296719) (← links)
- ACE2 hydrolyzes Angiotensin-(1-8) to Angiotensin-(1-7) (Q50296726) (← links)
- SARS-CoV-2 (Q82069695) (← links)
- SARS-CoV-1 (Q85438966) (← links)
- Structural basis for the recognition of the SARS-CoV-2 by full-length human ACE2 (Q87726414) (← links)
- The proximal origin of SARS-CoV-2 (Q87830056) (← links)
- spike glycoprotein [SARS-CoV-2] (Q87917585) (← links)
- Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target (Q88291889) (← links)
- SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor (Q88292103) (← links)
- ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19 (Q88978459) (← links)
- Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses (Q89866691) (← links)
- SARS-CoV-2 Spike - human ACE2 receptor complex (Q90012260) (← links)
- SARS-CoV-2 Spike - human ACE2-SLC6A19 complex (Q90012261) (← links)
- Angiotensin receptor blockers as tentative SARS-CoV-2 therapeutics (Q90027115) (← links)
- Angiotensin Converting Enzyme 2: SARS-CoV-2 Receptor and Regulator of the Renin-Angiotensin System (Q91703665) (← links)
- Cell entry mechanisms of SARS-CoV-2 (Q94589965) (← links)
- Pathogenesis of SARS-CoV-2 in transgenic mice expressing human angiotensin-converting enzyme 2 (Q95601060) (← links)
- Broad and differential animal ACE2 receptor usage by SARS-CoV-2 (Q95628508) (← links)
- TMPRSS2 and ACE2 Coexpression in SARS-CoV-2 Salivary Glands Infection (Q96031030) (← links)
- Single-cell RNA analysis on ACE2 expression provides insights into SARS-CoV-2 potential entry into the bloodstream and heart injury (Q96221150) (← links)
- Increased expression of ACE2, the SARS-CoV-2 entry receptor, in alveolar and bronchial epithelium of smokers and COPD subjects (Q97518534) (← links)
- The SARS-CoV-2 receptor, ACE-2, is expressed on many different cell types: implications for ACE-inhibitor- and angiotensin II receptor blocker-based antihypertensive therapies-reply (Q97529401) (← links)
- ACE2, TMPRSS2, and Furin variants and SARS-CoV-2 infection in Madrid, Spain (Q97638457) (← links)
- The D614G mutation in the SARS-CoV2 Spike protein increases infectivity in an ACE2 receptor dependent manner (Q98191474) (← links)
- Deep mutational scanning of SARS-CoV-2 receptor binding domain reveals constraints on folding and ACE2 binding (Q98720898) (← links)
- glycosylated-ACE2 [plasma membrane] (Q99978807) (← links)
- glycosylated-ACE2 [endocytic vesicle membrane] (Q99978824) (← links)