human | Q5 |
P496 | ORCID iD | 0000-0001-8097-3272 |
P734 | family name | Bernstein | Q21660706 |
Bernstein | Q21660706 | ||
Bernstein | Q21660706 | ||
P735 | given name | Kenneth | Q2492643 |
Kenneth | Q2492643 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q48402225 | A cDNA sequence encoding a rabbit heavy chain variable region of the VHa2 allotype showing homologies with human heavy chain sequences |
Q28146240 | A catalytically active Jak2 is required for the angiotensin II-dependent activation of Fyn |
Q57630655 | A deeply recessed active site in angiotensin-converting enzyme is indicated from the binding characteristics of biotin-spacer-inhibitor reagents |
Q52010851 | A functional Jak2 tyrosine kinase domain is essential for mouse development. |
Q24306614 | A modern understanding of the traditional and nontraditional biological functions of angiotensin-converting enzyme |
Q42143271 | A recombinant rat vascular AT1 receptor confers growth properties to angiotensin II in Chinese hamster ovary cells |
Q54594958 | ACE and ACE2 activity in diabetic mice. |
Q57630564 | ACE knockout mice - lessons for adult nephrology |
Q26866225 | ACE overexpression in myelomonocytic cells: effect on a mouse model of Alzheimer's disease |
Q57630597 | ANG II-induced tyrosine phosphorylation stimulates phospholipase C-gamma 1 and Cl-channels in mesangial cells |
Q57630610 | Angiotensin II Activates pp60 c- src in Vascular Smooth Muscle Cells |
Q57630605 | Angiotensin II Controls p21 Activity via pp60 |
Q57630587 | Angiotensin II Stimulates Tyrosine Phosphorylation and Activation of Insulin Receptor Substrate 1 and Protein-tyrosine Phosphatase 1D in Vascular Smooth Muscle Cells |
Q57630630 | Angiotensin II induces 3CH134, a protein-tyrosine phosphatase, in vascular smooth muscle cells |
Q35817958 | Angiotensin II receptor blockade or deletion of vascular endothelial ACE does not prevent vascular dysfunction and remodeling in 20-HETE-dependent hypertension |
Q57630567 | Angiotensin II signal transduction pathways |
Q57630626 | Angiotensin II stimulates tyrosine phosphorylation of phospholipase C-gamma 1 in vascular smooth muscle cells |
Q34086852 | Angiotensin-converting enzyme N-terminal inactivation alleviates bleomycin-induced lung injury |
Q34682525 | Angiotensin-converting enzyme is required for normal myelopoiesis |
Q35031960 | Angiotensin-converting enzyme overexpression in myelocytes enhances the immune response |
Q30572684 | Angiotensin-converting enzyme overexpression in myelomonocytes prevents Alzheimer's-like cognitive decline |
Q57630643 | Aortic and renal regulation of the renin-angiotensin system in interrenal aortic coarctation |
Q52346126 | BULLET: a computer simulation of shotgun DNA sequencing. |
Q57630646 | Bovine angiotensin converting enzyme cDNA cloning and regulation. Increased expression during endothelial cell growth arrest |
Q36803422 | CD70 Exacerbates Blood Pressure Elevation and Renal Damage in Response to Repeated Hypertensive Stimuli |
Q35176717 | Cardiac-restricted angiotensin-converting enzyme overexpression causes conduction defects and connexin dysregulation. |
Q48076875 | Chicken lacks the testis specific isozyme of angiotensin converting enzyme found in mammals |
Q27011524 | Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation |
Q34454645 | DC isoketal-modified proteins activate T cells and promote hypertension. |
Q28565959 | Dependence on the motif YIPP for the physical association of Jak2 kinase with the intracellular carboxyl tail of the angiotensin II AT1 receptor |
Q51022226 | Depletion of tissue angiotensin-converting enzyme differentially influences the intrarenal and urinary expression of angiotensin peptides. |
Q34786191 | Different in vivo functions of the two catalytic domains of angiotensin-converting enzyme (ACE). |
Q28301248 | Direct stimulation of Jak/STAT pathway by the angiotensin II AT1 receptor |
Q57630500 | EHRs can boost compliance |
Q44760479 | Effect of reduced angiotensin-converting enzyme gene expression and angiotensin-converting enzyme inhibition on angiotensin and bradykinin peptide levels in mice |
Q57630614 | Electroporation of pp60c−srcAntibodies Inhibits the Angiotensin II Activation of Phospholipase C-γ1 in Rat Aortic Smooth Muscle Cells |
Q36014052 | Establishing the role of angiotensin-converting enzyme in renal function and blood pressure control through the analysis of genetically modified mice |
Q48286185 | Evolutionary conservation of splice sites in sterile C mu transcripts and of immunoglobulin heavy chain (IgH) enhancer region sequences |
Q57630576 | Examining the renin-angiotensin system one hundred years after its discovery |
Q53769335 | Expression of nonmuscle myosin heavy chain-B isoform in the vessel wall of porcine coronary arteries after balloon angioplasty. |
Q52528253 | Expression of testis angiotensin-converting enzyme is mediated by a cyclic AMP responsive element. |
Q34196093 | Fibroblast growth factor stimulates angiotensin converting enzyme expression in vascular smooth muscle cells. Possible mediator of the response to vascular injury. |
Q35839992 | Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice |
Q57630547 | Genetic manipulation of the renin-angiotensin system |
Q35125969 | Genetic models provide unique insight into angiotensin and bradykinin peptides in the extravascular compartment of the heart in vivo |
Q36423068 | Germline VH genes in an a3 rabbit not typical of any one VHa allotype. |
Q57630619 | Glucocorticoids Induce Angiotensin-Converting Enzyme Expression in Vascular Smooth Muscle |
Q34580630 | Identification of prolyl carboxypeptidase as an alternative enzyme for processing of renal angiotensin II using mass spectrometry. |
Q57630622 | Identification of two positive transcriptional elements within the 91-base pair promoter for mouse testis angiotensin converting enzyme (testis ACE) |
Q27332212 | Immune activation caused by vascular oxidation promotes fibrosis and hypertension |
Q54878118 | Immune activation caused by vascular oxidation promotes fibrosis and hypertension. |
Q57630635 | Immunohistochemical localization of rat angiotensin II AT1 receptor |
Q44094428 | Impaired urine concentration and absence of tissue ACE: involvement of medullary transport proteins |
Q40977288 | Importance of tyrosine phosphorylation in angiotensin II type 1 receptor signaling. |
Q35696855 | Increased angiotensin II-induced hypertension and inflammatory cytokines in mice lacking angiotensin-converting enzyme N domain activity |
Q35580826 | Inhibition of c-Src tyrosine kinase prevents angiotensin II-mediated connexin-43 remodeling and sudden cardiac death. |
Q35165689 | Inhibition of renin-angiotensin system (RAS) reduces ventricular tachycardia risk by altering connexin43. |
Q57630554 | Insights derived from ACE knockout mice |
Q52237111 | Insulin-like growth factor I gene expression in vascular cells. |
Q34695342 | Intrarenal angiotensin-converting enzyme induces hypertension in response to angiotensin I infusion |
Q35581620 | Is angiotensin II a direct mediator of left ventricular hypertrophy? Time for another look |
Q48225244 | Isolation of a cDNA encoding the vascular type-1 angiotensin II receptor |
Q57630557 | Jak2 Acts as Both a STAT1 Kinase and as a Molecular Bridge Linking STAT1 to the Angiotensin II AT1Receptor |
Q44550669 | Janus kinase 2 determinants for growth hormone receptor association, surface assembly, and signaling |
Q36255786 | Kappa-chain allotypes and isotypes in the rabbit: cDNA sequences of clones encoding b9 suggest an evolutionary pathway and possible role of the interdomain disulfide bond in quantitative allotype expression |
Q50748561 | Male fertility is dependent on dipeptidase activity of testis ACE. |
Q57630524 | Mast Cells: The Missing Source of Cardiac Renin? |
Q57630540 | Mice Lacking Endothelial ACE |
Q57630545 | Mice Lacking Endothelial Angiotensin-Converting Enzyme Have a Normal Blood Pressure |
Q52909701 | Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility. |
Q35103181 | Mice with cardiac-restricted angiotensin-converting enzyme (ACE) have atrial enlargement, cardiac arrhythmia, and sudden death. |
Q35855609 | Mice with enhanced macrophage angiotensin-converting enzyme are resistant to melanoma. |
Q40856027 | Microglia participate in neurogenic regulation of hypertension |
Q57630517 | Micropuncture determination of nephron function in mice without tissue angiotensin-converting enzyme |
Q42455487 | Modulation of cardiac Ca2+ channel by Gq-activating neurotransmitters reconstituted in Xenopus oocytes. |
Q35237333 | Molecular analysis of the renin-angiotensin system |
Q36339127 | Mutation of Asp74 of the rat angiotensin II receptor confers changes in antagonist affinities and abolishes G-protein coupling. |
Q36202604 | Myeloid Suppressor Cells Accumulate and Regulate Blood Pressure in Hypertension |
Q41699873 | New insights into the cellular signaling of seven transmembrane receptors: the role of tyrosine phosphorylation. |
Q35205715 | Newer approaches to genetic modeling in mice: tissue-specific protein expression as studied using angiotensin-converting enzyme (ACE). |
Q35686205 | Newly recognized physiologic and pathophysiologic actions of the angiotensin-converting enzyme |
Q40128743 | Nodular (pseudosarcomatous) fasciitis, a nonrecurrent lesion: clinicopathologic study of 134 cases. |
Q35836666 | Nontraditional roles of angiotensin-converting enzyme |
Q48401034 | Nucleotide sequence of a rabbit IgG heavy chain from the recombinant F-I haplotype |
Q26750677 | Overexpression of angiotensin-converting enzyme in myelomonocytic cells enhances the immune response |
Q57630657 | Partial protein sequence of mouse and bovine kidney angiotensin converting enzyme |
Q36392598 | Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing |
Q45837123 | Promoter sequences of murine alpha A crystallin, murine alpha 2(I) collagen or of avian sarcoma virus genes linked to the bacterial chloramphenicol acetyl transferase gene direct tissue-specific patterns of chloramphenicol acetyl transferase express |
Q27004277 | Rediscovering ACE: novel insights into the many roles of the angiotensin-converting enzyme |
Q57630638 | Regulated Expression of Testis Angiotensin-Converting Enzyme during Spermatogenesis in Mice1 |
Q48446299 | Regulation of steady-state beta-amyloid levels in the brain by neprilysin and endothelin-converting enzyme but not angiotensin-converting enzyme |
Q26827777 | Renal angiotensin-converting enzyme and blood pressure control |
Q34568769 | Renal angiotensin-converting enzyme is essential for the hypertension induced by nitric oxide synthesis inhibition |
Q34775600 | Renal generation of angiotensin II and the pathogenesis of hypertension |
Q54784257 | Role of bradykinin in angiotensin-converting enzyme knockout mice. |
Q36780988 | Salt Sensitivity in Response to Renal Injury Requires Renal Angiotensin-Converting Enzyme |
Q30412851 | Sequence of a cDNA encoding Basilea kappa light chains (K2 isotype) suggests a possible relationship of protein structure to limited expression |
Q48105484 | Sequence of a cDNA encoding dog insulin-like growth factor I. |
Q36157768 | Six truisms concerning ACE and the renin-angiotensin system educed from the genetic analysis of mice |
Q36658161 | Sperm-specific expression of angiotensin-converting enzyme (ACE) is mediated by a 91-base-pair promoter containing a CRE-like element |
Q44408035 | Targeting bacteriophage T7 RNA polymerase to the mammalian cell nucleus |
Q35199729 | Targeting genes for self-excision in the germ line |
Q57630629 | The Angiotensin II AT1 Receptor Is Tyrosine and Serine Phosphorylated and can Serve as a Substrate for the SRC Family of Tyrosine Kinases |
Q57630561 | The Angiotensin II–Dependent Association of Jak2 and c-Src Requires the N-Terminus of Jak2 and the SH2 Domain of c-Src |
Q47772851 | The Importance of Tyrosine Phosphorylation in Angiotensin II Signaling |
Q36605185 | The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA. |
Q35229303 | The Renin-Angiotensin System: A Biological Machine |
Q57630584 | The Role of Angiotensin-Converting Enzyme in Blood Pressure Control, Renal Function, and Male Fertility |
Q31816068 | The angiotensin II-dependent nuclear translocation of Stat1 is mediated by the Jak2 protein motif 231YRFRR. |
Q40779253 | The biology of angiotensin II receptors. |
Q35402189 | The carboxypeptidase ACE shapes the MHC class I peptide repertoire |
Q37367283 | The critical role of tissue angiotensin-converting enzyme as revealed by gene targeting in mice |
Q39519165 | The distribution of cadmium-115m chloride, cobalt-57 bleomycin, iodine-125 human serum albumin, selenium-75 selenite and selenomethionine-75 in a rat hepatoma model |
Q57630579 | The functional role of angiotensin-converting enzyme as explored by using knockout mice |
Q28645954 | The genomic organization of the rat AT1 angiotensin receptor |
Q27025017 | The intrarenal generation of angiotensin II is required for experimental hypertension |
Q35050809 | The peptide network regulated by angiotensin converting enzyme (ACE) in hematopoiesis |
Q57630551 | The role of Ca2+ mobilization and heterotrimeric G protein activation in mediating tyrosine phosphorylation signaling patterns in vascular smooth muscle cells |
Q57630569 | The role of tissue angiotensin-converting enzyme (ACE): studies of ACE mutant mice |
Q41120444 | The role of tyrosine phosphorylation in angiotensin II mediated intracellular signaling and cell growth. |
Q35690161 | The sequences of rabbit kappa light chains of b4 and b5 allotypes differ more in their constant regions than in their 3' untranslated regions. |
Q40075558 | The structural and genetic basis for expression of normal and latent VHa allotypes of the rabbit |
Q35781354 | The use of knockout mouse technology to achieve tissue selective expression of angiotensin converting enzyme |
Q57630599 | Tissue Specific Expression of Testis Angiotensin Converting Enzyme is Not Determined by the −32 Nonconsensus TATA Motif |
Q57630652 | Tissue specific expression of angiotensin converting enzyme |
Q36468153 | Tissue specific expression of angiotensin converting enzyme: a new way to study an old friend |
Q33925020 | Transcription of testicular angiotensin-converting enzyme (ACE) is initiated within the 12th intron of the somatic ACE gene |
Q48214450 | Transgenic mice demonstrate a testis-specific promoter for angiotensin-converting enzyme |
Q52597129 | Two ACEs and a heart. |
Q24650649 | Uncoupled cardiac nitric oxide synthase mediates diastolic dysfunction |
Q36347239 | Views of the renin-angiotensin system: brilling, mimsy, and slithy tove |
Q37232479 | cAMP-response element modulator tau is a positive regulator of testis angiotensin converting enzyme transcription. |