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  1. Article: Editorial: Proteins and protein-complexes underlying mitochondrial structure-function and metabolism: implications in diseases.

    Sabbir, Mohammad Golam / Dar, Nawab John / Bhat, Shahnawaz Ali / Alanazi, Hamad H / Perry, Jeff

    Frontiers in cell and developmental biology

    2024  Volume 12, Page(s) 1386787

    Language English
    Publishing date 2024-03-04
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2737824-X
    ISSN 2296-634X
    ISSN 2296-634X
    DOI 10.3389/fcell.2024.1386787
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Advance Consent in Acute Stroke Trials: Survey of Canadian Research Ethics Board Chairs.

    Seeger, Rena / Udoh, Ubong / Dewar, Brian / Nicholls, Stuart / Fedyk, Mark / Fahed, Robert / Perry, Jeff / Hill, Michael D / Menon, Bijoy / Swartz, Richard H / Poppe, Alexandre Y / Gocan, Sophia / Brehaut, Jamie / Dainty, Katie / Shepherd, Victoria / Dowlatshahi, Dar / Shamy, Michel

    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

    2023  Volume 51, Issue 2, Page(s) 285–288

    Abstract: Advance consent could allow individuals at high risk of stroke to provide consent before they might become eligible for enrollment in acute stroke trials. This survey explores the acceptability of this novel technique to Canadian Research Ethics Board ( ... ...

    Abstract Advance consent could allow individuals at high risk of stroke to provide consent before they might become eligible for enrollment in acute stroke trials. This survey explores the acceptability of this novel technique to Canadian Research Ethics Board (REB) chairs that review acute stroke trials. Responses from 15 REB chairs showed that majority of respondents expressed comfort approving studies that adopt advance consent. There was no clear preference for advance consent over deferral of consent, although respondents expressed significant concern with broad rather than trial-specific advance consent. These findings shed light on the acceptability of advance consent to Canadian ethics regulators.
    MeSH term(s) Humans ; Canada ; Ethics, Research ; Surveys and Questionnaires ; Stroke/therapy ; Informed Consent
    Language English
    Publishing date 2023-07-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 197622-9
    ISSN 0317-1671
    ISSN 0317-1671
    DOI 10.1017/cjn.2023.247
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Advance Consent in Acute Stroke Trials: Survey of Canadian Stroke Physicians.

    Udoh, Ubong / Dewar, Brian / Nicholls, Stuart / Fedyk, Mark / Fahed, Robert / Perry, Jeff / Hill, Michael D / Menon, Bijoy / Swartz, Richard H / Poppe, Alexandre Y / Gocan, Sophia / Brehaut, Jamie / Dainty, Katie / Shepherd, Victoria / Dowlatshahi, Dar / Shamy, Michel

    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

    2023  Volume 51, Issue 1, Page(s) 122–125

    Abstract: Advance consent presents a potential solution to the challenge of obtaining informed consent for participation in acute stroke trials. Clinicians in stroke prevention clinics are uniquely positioned to identify and seek consent from potential stroke ... ...

    Abstract Advance consent presents a potential solution to the challenge of obtaining informed consent for participation in acute stroke trials. Clinicians in stroke prevention clinics are uniquely positioned to identify and seek consent from potential stroke trial participants. To assess the acceptability of advance consent to Canadian stroke clinic physicians, we performed an online survey. We obtained 58 respondents (response rate 35%): the vast majority (82%) expressed comfort with obtaining advance consent and 92% felt that doing so would not be a significant disruption to clinic workflow. These results support further study of advance consent for acute stroke trials.
    MeSH term(s) Humans ; Informed Consent ; Canada ; Stroke/therapy ; Physicians ; Surveys and Questionnaires
    Language English
    Publishing date 2023-02-17
    Publishing country England
    Document type Journal Article
    ZDB-ID 197622-9
    ISSN 0317-1671
    ISSN 0317-1671
    DOI 10.1017/cjn.2023.12
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: S100B protein level for the detection of clinically significant intracranial haemorrhage in patients with mild traumatic brain injury: a subanalysis of a prospective cohort study.

    Blais Lécuyer, Julien / Mercier, Éric / Tardif, Pier-Alexandre / Archambault, Patrick M / Chauny, Jean-Marc / Berthelot, Simon / Frenette, Jérôme / Perry, Jeff / Stiell, Ian / Émond, Marcel / Lee, Jacques / Lang, Eddy / McRae, Andrew / Boucher, Valérie / Le Sage, Natalie

    Emergency medicine journal : EMJ

    2020  Volume 38, Issue 4, Page(s) 285–289

    Abstract: Background: Clinical assessment of patients with mild traumatic brain injury (mTBI) is challenging and overuse of head CT in the ED is a major problem. Several studies have attempted to reduce unnecessary head CTs following a mTBI by identifying new ... ...

    Abstract Background: Clinical assessment of patients with mild traumatic brain injury (mTBI) is challenging and overuse of head CT in the ED is a major problem. Several studies have attempted to reduce unnecessary head CTs following a mTBI by identifying new tools aiming to predict intracranial bleeding. Higher levels of S100B protein have been associated with intracranial haemorrhage following a mTBI in previous literature. The main objective of this study is to assess whether plasma S100B protein level is associated with clinically significant brain injury and could be used to reduce the number of head CT post-mTBI.
    Methods: Study design:
    Results: 476 patients were included. Mean age was 41±18 years old and 150 (31.5%) were women. Twenty-four (5.0%) patients had a clinically significant intracranial haemorrhage. Thirteen patients (2.7%) presented a non-clinically significant brain injury. A total of 37 (7.8%) brain injured patients were included in our study. S100B median value (Q1-Q3) was: 0.043 µg/L (0.008-0.080) for patients with clinically important brain injury versus 0.039 µg/L (0.023-0.059) for patients without clinically important brain injury. Sensitivity and specificity of the S100B protein level, if used alone to detect clinically important brain injury, were 16.7% (95% CI 4.7% to 37.4%) and 88.5% (95% CI 85.2% to 91.3%), respectively.
    Conclusion: Plasma S100B protein level was not associated with clinically significant intracranial lesion in patients with mTBI.
    MeSH term(s) Adult ; Aged ; Brain Concussion/complications ; Brain Concussion/epidemiology ; Cohort Studies ; Enzyme-Linked Immunosorbent Assay/methods ; Female ; Humans ; Injury Severity Score ; Intracranial Hemorrhages/blood ; Intracranial Hemorrhages/diagnosis ; Intracranial Hemorrhages/etiology ; Male ; Middle Aged ; Ontario ; Prospective Studies ; S100 Calcium Binding Protein beta Subunit/analysis ; S100 Calcium Binding Protein beta Subunit/blood
    Chemical Substances S100 Calcium Binding Protein beta Subunit ; S100B protein, human
    Language English
    Publishing date 2020-12-18
    Publishing country England
    Document type Journal Article ; Multicenter Study
    ZDB-ID 2040124-3
    ISSN 1472-0213 ; 1472-0205
    ISSN (online) 1472-0213
    ISSN 1472-0205
    DOI 10.1136/emermed-2020-209583
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Peripheral Nerve Blocks and Potentially Attributable Adverse Events in Older People with Hip Fracture: A Retrospective Population-based Cohort Study.

    Melton, Natalie / Talarico, Robert / Abdallah, Faraj / Beaulé, Paul E / Boet, Sylvain / Forster, Alan J / Fernando, Shannon M / Huang, Allen / McCartney, Colin J L / Meulenkamp, Bradley / Perry, Jeff / Power, Barbara / Ramlogan, Reva / Taljaard, Monica / Tanuseputro, Peter / van Walraven, Carl / Wijeysundera, Duminda N / McIsaac, Daniel I

    Anesthesiology

    2021  Volume 135, Issue 3, Page(s) 454–462

    Language English
    Publishing date 2021-07-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 269-0
    ISSN 1528-1175 ; 0003-3022
    ISSN (online) 1528-1175
    ISSN 0003-3022
    DOI 10.1097/ALN.0000000000003863
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Real-time Visualization of Breast Carcinoma in Pathology Specimens From Patients Receiving Fluorescent Tumor-Marking Agent Tozuleristide.

    Dintzis, Suzanne M / Hansen, Stacey / Harrington, Kristi M / Tan, Lennart C / Miller, Dennis M / Ishak, Laura / Parrish-Novak, Julia / Kittle, David / Perry, Jeff / Gombotz, Carolyn / Fortney, Tina / Porenta, Stephanie / Hales, Lisa / Calhoun, Kristine E / Anderson, Benjamin O / Javid, Sara H / Byrd, David R

    Archives of pathology & laboratory medicine

    2018  Volume 143, Issue 9, Page(s) 1076–1083

    Abstract: Context.—: Resection of breast carcinoma with adequate margins reduces the risk of local recurrence and reoperation. Tozuleristide (BLZ-100) is an investigational peptide-fluorophore agent that may aid in intraoperative tumor detection and margin ... ...

    Abstract Context.—: Resection of breast carcinoma with adequate margins reduces the risk of local recurrence and reoperation. Tozuleristide (BLZ-100) is an investigational peptide-fluorophore agent that may aid in intraoperative tumor detection and margin assessment. In this study, fluorescence imaging was conducted ex vivo on gross breast pathology specimens.
    Objectives.—: To determine the potential of tozuleristide to detect breast carcinoma in fresh pathology specimens and the feasibility of fluorescence-guided intraoperative pathology assessment of surgical margins.
    Design.—: Twenty-three patients received an intravenous bolus dose of 6 or 12 mg of tozuleristide at least 1 hour before surgery. Fifteen lumpectomy and 12 mastectomy specimens were evaluated for fluorescence by the site's clinical pathology staff using the SIRIS, an investigational near-infrared imaging device. The breast tissue was then processed per usual procedures. Fluorescent patterns were correlated with the corresponding hematoxylin-eosin-stained sections. Clinical pathology reports were used to correlate fluorescent signal to grade, histotype, prognostic marker status, and margin measurements.
    Results.—: Tozuleristide fluorescence was readily observed in invasive and in situ breast carcinoma specimens. Most invasive carcinomas were bright and focal, whereas in situ lesions demonstrated a less intense, more diffuse pattern. Tozuleristide was detected in ductal and lobular carcinomas with a similar fluorescent pattern. Fluorescence was detected in high- and low-grade lesions, and molecular marker/hormone receptor status did not affect signal. Fluorescence could be used to identify the relationship of carcinoma to margins intraoperatively.
    Conclusions.—: Tumor targeting with tozuleristide allowed visual real-time distinction between pathologically confirmed breast carcinoma and normal tissue.
    MeSH term(s) Breast Carcinoma In Situ/diagnostic imaging ; Breast Carcinoma In Situ/pathology ; Breast Carcinoma In Situ/surgery ; Breast Neoplasms/diagnostic imaging ; Breast Neoplasms/surgery ; Carcinoma, Ductal, Breast/diagnostic imaging ; Carcinoma, Ductal, Breast/pathology ; Carcinoma, Ductal, Breast/surgery ; Carcinoma, Lobular/diagnostic imaging ; Carcinoma, Lobular/pathology ; Carcinoma, Lobular/surgery ; Female ; Fluorescent Dyes ; Humans ; Indocyanine Green/analogs & derivatives ; Intraoperative Care/methods ; Margins of Excision ; Mastectomy ; Mastectomy, Segmental ; Neoplasm Invasiveness/diagnostic imaging ; Neoplasm Invasiveness/pathology ; Prognosis ; Scorpion Venoms
    Chemical Substances Fluorescent Dyes ; Scorpion Venoms ; Chlorotoxin (06UV5RFW57) ; tozuleristide (835UH424TU) ; Indocyanine Green (IX6J1063HV)
    Language English
    Publishing date 2018-12-14
    Publishing country United States
    Document type Clinical Trial, Phase I ; Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 194119-7
    ISSN 1543-2165 ; 0363-0153 ; 0096-8528 ; 0003-9985
    ISSN (online) 1543-2165
    ISSN 0363-0153 ; 0096-8528 ; 0003-9985
    DOI 10.5858/arpa.2018-0197-OA
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Phase 1 Safety, Pharmacokinetics, and Fluorescence Imaging Study of Tozuleristide (BLZ-100) in Adults With Newly Diagnosed or Recurrent Gliomas.

    Patil, Chirag G / Walker, David G / Miller, Dennis M / Butte, Pramod / Morrison, Beth / Kittle, David S / Hansen, Stacey J / Nufer, Kaitlin L / Byrnes-Blake, Kelly A / Yamada, Miko / Lin, Lynlee L / Pham, Kim / Perry, Jeff / Parrish-Novak, Julia / Ishak, Laura / Prow, Tarl / Black, Keith / Mamelak, Adam N

    Neurosurgery

    2019  Volume 85, Issue 4, Page(s) E641–E649

    Abstract: Background: Fluorescence-guided surgery (FGS) can improve extent of resection in gliomas. Tozuleristide (BLZ-100), a near-infrared imaging agent composed of the peptide chlorotoxin and a near-infrared fluorophore indocyanine green, is a candidate ... ...

    Abstract Background: Fluorescence-guided surgery (FGS) can improve extent of resection in gliomas. Tozuleristide (BLZ-100), a near-infrared imaging agent composed of the peptide chlorotoxin and a near-infrared fluorophore indocyanine green, is a candidate molecule for FGS of glioma and other tumor types.
    Objective: To perform a phase 1 dose-escalation study to characterize the safety, pharmacokinetics, and fluorescence imaging of tozuleristide in adults with suspected glioma.
    Methods: Patients received a single intravenous dose of tozuleristide 3 to 29 h before surgery. Fluorescence images of tumor and cavity in Situ before and after resection and of excised tissue ex Vivo were acquired, along with safety and pharmacokinetic measures.
    Results: A total of 17 subjects received doses between 3 and 30 mg. No dose-limiting toxicity was observed, and no reported adverse events were considered related to tozuleristide. At doses of 9 mg and above, the terminal serum half-life for tozuleristide was approximately 30 min. Fluorescence signal was detected in both high- and low-grade glial tumors, with high-grade tumors generally showing greater fluorescence intensity compared to lower grade tumors. In high-grade tumors, signal intensity increased with increased dose levels of tozuleristide, regardless of the time of dosing relative to surgery.
    Conclusion: These results support the safety of tozuleristide at doses up to 30 mg and suggest that tozuleristide imaging may be useful for FGS of gliomas.
    MeSH term(s) Adult ; Aged ; Brain Neoplasms/diagnostic imaging ; Brain Neoplasms/metabolism ; Brain Neoplasms/surgery ; Dose-Response Relationship, Drug ; Female ; Fluorescent Dyes/administration & dosage ; Fluorescent Dyes/pharmacokinetics ; Glioma/diagnostic imaging ; Glioma/metabolism ; Glioma/surgery ; Humans ; Indocyanine Green/administration & dosage ; Indocyanine Green/analogs & derivatives ; Indocyanine Green/pharmacokinetics ; Injections, Intravenous ; Male ; Middle Aged ; Neoplasm Recurrence, Local/diagnostic imaging ; Neoplasm Recurrence, Local/metabolism ; Neoplasm Recurrence, Local/surgery ; Optical Imaging/methods ; Scorpion Venoms/administration & dosage ; Scorpion Venoms/pharmacokinetics
    Chemical Substances Fluorescent Dyes ; Scorpion Venoms ; tozuleristide (835UH424TU) ; Indocyanine Green (IX6J1063HV)
    Language English
    Publishing date 2019-05-08
    Publishing country United States
    Document type Clinical Trial, Phase I ; Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 135446-2
    ISSN 1524-4040 ; 0148-396X
    ISSN (online) 1524-4040
    ISSN 0148-396X
    DOI 10.1093/neuros/nyz125
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  8. Article ; Online: The effect of early in-hospital medication review on health outcomes: a systematic review.

    Hohl, Corinne M / Wickham, Maeve E / Sobolev, Boris / Perry, Jeff J / Sivilotti, Marco L A / Garrison, Scott / Lang, Eddy / Brasher, Penny / Doyle-Waters, Mary M / Brar, Baljeet / Rowe, Brian H / Lexchin, Joel / Holland, Richard

    British journal of clinical pharmacology

    2015  Volume 80, Issue 1, Page(s) 51–61

    Abstract: Aims: Adverse drug events are an important cause of emergency department visits, unplanned admissions and prolonged hospital stays. Our objective was to synthesize the evidence on the effect of early in-hospital pharmacist-led medication review on ... ...

    Abstract Aims: Adverse drug events are an important cause of emergency department visits, unplanned admissions and prolonged hospital stays. Our objective was to synthesize the evidence on the effect of early in-hospital pharmacist-led medication review on patient-oriented outcomes based on observed data.
    Methods: We systematically searched eight bibliographic reference databases, electronic grey literature, medical journals, conference proceedings, trial registries and bibliographies of relevant papers. We included studies that employed random or quasi-random methods to allocate subjects to pharmacist-led medication review or control. Medication review had to include, at a minimum, obtaining a best possible medication history and reviewing medications for appropriateness and adverse drug events. The intervention had to be initiated within 24 h of emergency department presentation or 72 h of admission. We extracted data in duplicate and pooled outcomes from clinically homogeneous studies of the same design using random effects meta-analysis.
    Results: We retrieved 4549 titles of which seven were included, reporting the outcomes of 3292 patients. We pooled data from studies of the same design, and found no significant differences in length of hospital admission (weighted mean difference [WMD] -0.04 days, 95% confidence interval [CI] -1.63, 1.55), mortality (odds ratio [OR] 1.09, 95% CI 0.69, 1.72), readmissions (OR 1.15, 95% CI 0.81, 1.63) or emergency department revisits at 3 months (OR 0.60, 95% CI 0.27, 1.32). Two large studies reporting reductions in readmissions could not be included in our pooled estimates due to differences in study design.
    Conclusions: Wide confidence intervals suggest that additional research is likely to influence the effect size estimates and clarify the effect of medication review on patient-oriented outcomes. This systematic review failed to identify an effect of pharmacist-led medication review on health outcomes.
    MeSH term(s) Drug-Related Side Effects and Adverse Reactions/prevention & control ; Hospitalization/statistics & numerical data ; Humans ; Medication Systems, Hospital
    Language English
    Publishing date 2015-07
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/bcp.12585
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  9. Article ; Online: Stratified, urgent care for transient ischemic attack results in low stroke rates.

    Wasserman, Jason / Perry, Jeff / Dowlatshahi, Dar / Stotts, Grant / Stiell, Ian / Sutherland, Jane / Symington, Cheryl / Sharma, Mukul

    Stroke

    2010  Volume 41, Issue 11, Page(s) 2601–2605

    Abstract: Background and purpose: Transient ischemic attack (TIA) is a marker for early risk of stroke. No previous studies have assessed the use of urgent stroke prevention clinics for emergency department (ED) patients with TIA. We hypothesized that an ABCD2- ... ...

    Abstract Background and purpose: Transient ischemic attack (TIA) is a marker for early risk of stroke. No previous studies have assessed the use of urgent stroke prevention clinics for emergency department (ED) patients with TIA. We hypothesized that an ABCD2-based ED triaging tool for TIA with outpatient management would be associated with lower 90-day stroke rate than that predicted by ABCD2.
    Methods: A cohort of prospectively identified patients presenting with symptoms suggestive of TIA seen in 2 tertiary-care EDs. These patients were divided into 3 strata based on their ACBD2 score, and triage targets were set for each stratum. All patients received the same standard of care in the Stroke Clinic regardless of their risk score. Primary outcome was stroke by 90 days of index TIA. Secondary outcomes were subsequent TIA, myocardial infarction, or death.
    Results: One-thousand ninety-three patients met the inclusion criteria; 982 patients completed 90-day follow-up and comprised the final cohort. After stratification, 32%, 49%, and 19% of patients were categorized as low-, moderate-, or high-risk, respectively. The overall 90-day risk of stroke in all patients was 3.2%, compared with the ABCD2-predicted risk of 9.2%. Only 1.6% of patients with TIA/minor stroke were admitted from the ED. The risk of subsequent TIA, myocardial infarction, or death by 90 days was 5.5%, 0.1%, and 1.7%, respectively.
    Conclusions: Outpatient care in a rapid-access stroke prevention clinic using the ABCD2 score for triage resulted in a low 90-day stroke rate for patients in the ED with TIA. Benefit occurred without requiring admission for most patients.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Ambulatory Care ; Cohort Studies ; Emergency Service, Hospital ; Female ; Follow-Up Studies ; Humans ; Incidence ; Ischemic Attack, Transient/complications ; Ischemic Attack, Transient/therapy ; Male ; Middle Aged ; Ontario ; Prospective Studies ; Risk Factors ; Severity of Illness Index ; Stroke/epidemiology ; Stroke/prevention & control ; Time Factors ; Triage
    Language English
    Publishing date 2010-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80381-9
    ISSN 1524-4628 ; 0039-2499 ; 0749-7954
    ISSN (online) 1524-4628
    ISSN 0039-2499 ; 0749-7954
    DOI 10.1161/STROKEAHA.110.586842
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  10. Article ; Online: PRMT1-mediated FLT3 arginine methylation promotes maintenance of FLT3-ITD

    He, Xin / Zhu, Yinghui / Lin, Yi-Chun / Li, Min / Du, Juan / Dong, Haojie / Sun, Jie / Zhu, Lei / Wang, Hanying / Ding, Zonghui / Zhang, Lei / Zhang, Lianjun / Zhao, Dandan / Wang, Zhihao / Wu, Herman / Zhang, Han / Jiang, Wenjuan / Xu, Yang / Jin, Jian /
    Shen, Yudao / Perry, Jeff / Zhao, Xinyang / Zhang, Bin / Liu, Songbai / Xue, Sheng-Li / Shen, Binghui / Chen, Chun-Wei / Chen, Jianjun / Khaled, Samer / Kuo, Ya-Huei / Marcucci, Guido / Luo, Yun / Li, Ling

    Blood

    2019  Volume 134, Issue 6, Page(s) 548–560

    Abstract: The presence of FMS-like receptor tyrosine kinase-3 internal tandem duplication (FLT3-ITD) mutations in patients with acute myeloid leukemia (AML) is associated with poor clinical outcome. FLT3 tyrosine kinase inhibitors (TKIs), although effective in ... ...

    Abstract The presence of FMS-like receptor tyrosine kinase-3 internal tandem duplication (FLT3-ITD) mutations in patients with acute myeloid leukemia (AML) is associated with poor clinical outcome. FLT3 tyrosine kinase inhibitors (TKIs), although effective in kinase ablation, do not eliminate primitive FLT3-ITD
    MeSH term(s) Animals ; Arginine/metabolism ; Biomarkers, Tumor ; Catalysis ; Disease Models, Animal ; Gene Duplication ; Gene Expression Profiling ; Humans ; Leukemia, Myeloid, Acute/genetics ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/mortality ; Leukemia, Myeloid, Acute/pathology ; Methylation ; Mice ; Mice, Knockout ; Models, Molecular ; Prognosis ; Protein Binding ; Protein Conformation ; Protein Kinase Inhibitors/pharmacology ; Protein Kinase Inhibitors/therapeutic use ; Protein-Arginine N-Methyltransferases/antagonists & inhibitors ; Protein-Arginine N-Methyltransferases/chemistry ; Protein-Arginine N-Methyltransferases/metabolism ; Repressor Proteins/antagonists & inhibitors ; Repressor Proteins/chemistry ; Repressor Proteins/metabolism ; Xenograft Model Antitumor Assays ; fms-Like Tyrosine Kinase 3/chemistry ; fms-Like Tyrosine Kinase 3/genetics ; fms-Like Tyrosine Kinase 3/metabolism
    Chemical Substances Biomarkers, Tumor ; Protein Kinase Inhibitors ; Repressor Proteins ; Arginine (94ZLA3W45F) ; PRMT1 protein, human (EC 2.1.1.319) ; Protein-Arginine N-Methyltransferases (EC 2.1.1.319) ; FLT3 protein, human (EC 2.7.10.1) ; fms-Like Tyrosine Kinase 3 (EC 2.7.10.1)
    Language English
    Publishing date 2019-06-19
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2019001282
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