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Test Number : PMI-ACP
Test Name : PMI Agile Certified Practitioner
Vendor Name : PMI
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PMI-ACP test Format | PMI-ACP Course Contents | PMI-ACP Course Outline | PMI-ACP test Syllabus | PMI-ACP test Objectives

There are 120 questions for the PMI-ACP test (20 random questions (called as pre-test) from the 120 questions are not to be counted towards the final score)
All questions are multiple-choice questions with 1 correct answer from 4 choices
The PMI-ACP test lasts for 3 hours
The PMI-ACP test is computer-based in most cases (i.e. to be answered on a computer in a selected test centre)

Domain I. Agile Principles and Mindset 16%
Domain II. Value-driven Delivery 20%
Domain III. Stakeholder Engagement 17%
Domain IV. Team Performance 16%
Domain V. Adaptive Planning 12%
Domain VI. Problem Detection and Resolution 10%
Domain VII. Continuous Improvement (Product, Process, People) 9%


Domain I. Agile Principles and Mindset (9 tasks)
Explore, embrace, and apply agile principles and mindset within the context of the project team and organization.

Domain II. Value-Driven Delivery (4 sub-domains, 14 tasks)
Deliver valuable results by producing high-value increments for review, early and often, based on stakeholder priorities. Have the stakeholders provide feedback on these increments,and use this feedback to prioritize and Excellerate future increments.

Domain III. Stakeholder Engagement (3 sub-domains, 9 tasks)
Engage current and future interested parties by building a trusting environment that aligns their needs and expectations and balances their requests with an understanding of the cost/effort involved. Promote participation and collaboration throughout the project life cycle and provide the tools for effective and informed decision making.

Domain IV. Team Performance (3 sub-domains, 9 tasks)
Create an environment of trust, learning, collaboration, and conflict resolution that promotes team self-organization, enhances relationships among team members, and cultivates a culture of high performance.

Domain V. Adaptive Planning (3 sub-domains, 10 tasks)
Produce and maintain an evolving plan, from initiation to closure, based on goals, values, risks, constraints, stakeholder feedback, and review findings.

Domain VI. Problem Detection and Resolution (5 tasks)
Continuously identify problems, impediments, and risks; prioritize and resolve in a timely manner; monitor and communicate the problem resolution status; and implement process improvements to prevent them from occurring again.

Domain VII. Continuous Improvement (Product, Process, People) (6 tasks)
Continuously Excellerate the quality, effectiveness, and value of the product, the process, and the team.

Agile values and principles
=> Agile frameworks and terminology
=> Agile methods and approaches
=> Assessing and incorporating community and stakeholder values
=> Stakeholder management
=> Communication management
=> Facilitation methods
=> Knowledge sharing/written communication
=> Leadership
=> Building agile teams
=> Team motivation
=> Physical and virtual co-location
=> Global, cultural, and team diversity
=> Training, coaching, and mentoring
=> Developmental mastery models (for example, Tuckman, Dreyfus, Shu Ha Ri)
=> Self-assessment tools and techniques
=> Participatory decision models (for example, convergent, shared collaboration)
=> Principles of systems thinking (for example, complex adaptive, chaos)
=> Problem solving
=> Prioritization
=> Incremental delivery
=> Agile discovery
=> Agile sizing and estimation
=> Value based analysis and decomposition
=> Process analysis
=> Continuous improvement
=> Agile hybrid models
=> Managing with agile KPIs
=> Agile project chartering
=> Agile contracting
=> Agile project accounting principles
=> Regulatory compliance
=> PMI's Code of Ethics and Professional Conduct

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PMI test format

Biomarkers of myocardial damage in rats after cantharidin poisoning: utility for postmortem diagnosis and estimation of postmortem interval | PMI-ACP braindump questions and test dumps

Postmortem pathological alterations of rat hearts

In forensic identification work, the analysis of cantharidin-induced myocardial damage is usually stylish on the histopathologic examination. although, event indicates that pathological alterations can alternate over time because of the autolysis of coronary heart after dying. In their existing analyze, myocardial contraction band necrosis, inflammatory mobilephone infiltration and hemorrhage within the subendocardial have been accompanied in cantharidin-treated rats within forty eight h after demise whereas these changes were complex to determine because of the autolysis of myocardium 72 h after loss of life. due to this fact, to explore the biomarkers of myocardial injury in rats after cantharidin poisoning may be a solution to the issue.

Postmortem adjustments in TN-T, VEGF, HIF-1α, VEGF/TN-T, HIF-1α/TN-T, VEGF/HIF-1α and utility for postmortem prognosis

In their existing look at, the higher expression of TN-T were present in rats died of cantharidin poisoning and TN-T degrees have been strong in each time interval after loss of life, which suggested TN-T is a potential postmortem biomarker of mycardial damage caused by way of cantharidin poisoning. Most previous studies concentrated on the diagnostic role of postmortem TN-T in sufferers with acute myocardial infarction or unexpected cardiac loss of life and located the elevation of TN-T expression might also depend on the severity of ischemic myocardial damage13,14,25, which changed into consisted with the outcomes of the existing examine. in addition, their statistics showed that the TN-T ranges in postmortem remained reliable for up to 168 h after loss of life, which is over the 48 h said in previous. however, the accuracy and specificity of TN-T expression in postmortem diagnosis with some controversy16,18, and the effects of the ROC curve in their look at showed that the diagnostic accuracy of TN-T was seventy eight.09% which demonstrated previous foundings on TN-T is a selected and valuable cardiac biomarker for postmortem diagnosis of myocardial damage.

variations in total expression of VEGF inside 168 h after demise between in handle and in experimental have been now not found nevertheless it introduced an multiplied trend in their examine, the difference of VEGF expression between both companies became simplest present in the community of 168 h. The effects of previous studes on VEGF expression in human myocardial tissue showed that no statistical variations for expression have been detected whereas VEGF gene expression in physique fluids have been found at PMI intervals of over 12 h; despite the fact, their information recommended that the postmortem adjustments of VEGF protein expression in cardiac blood skilled the manner of descending then ascending and the valley value became within the neighborhood of 48 h; As outlined above, they believe that the postmortem changes of VEGF may well be is dependent upon the reason for dying and strategies of detection26,27.

Our latest look at indicated that postmortem alterations of HIF-1α expression changed into good each in handle and experimental within seventy two h after death. The HIF-1α stages in experimental neighborhood changed into decreased 48 h after death and the ameliorations turned into found in the group of seventy two h compared with control; which changed into supported by using the foundings of Fais P et al. that HIF-1α expression turned into gradually reduced in samples amassed four–5 days after demise and it turned into no longer detected 8–9 days after death28. in order that the postmortem diagnostic role of HIF-1α want more lengthy-time period observation over 168 h after death to greater accurate conclusions.

The outcomes of postmortem adjustments in VEGF/TN-T, HIF-1α/TN-T and VEGF/HIF-1α confirmed that HIF-1α/TN-T may be a cardiac biomarker for postmortem diagnosis of myocardial injury with the 70.37% diagnostic accuracy; And they also found that all the ratios had been reliable in handle after dying in each and every time interval; while the ratios of VEGF/TN-T and VEGF/HIF-1α have been accelerated over 72 h after loss of life in experimental, and the postmortem diagnostic position of them also need extra long-time period remark to evaluate. what is important, they found that the look at on diagnostic role of the ratios isn't outlined in old.

in this area, they found that TN-T and HIF-1α/TN-T are cardiac biomarkers for postmortem prognosis of cantharidin-triggered myocardial harm, and other biomarkers have potiencial value within the postmortem diagnosis in distinctive time intervals after dying. These interesting outcomes may additionally supply forensic pathologists with a reference to the postmoterm analysis of myocardial injury; And they hope that with greater lengthy-time period statement and the verification of those biomarkers in other forms of myocardial damage, the biomarkers in their study may well be used within the postmorterm diagnosis of myocardial damage in future.

affiliation between TN-T, VEGF, HIF-1α, VEGF/TN-T, HIF-1α/TN-T, VEGF/HIF-1α and PMI

PMI estimation continues to be a challenge in the forensic identification due to the lack of effective methods. As they comprehend, forensic protein know-how has been used to estimate the PMI for decades; and a lot of old studies concentrated on the postmortem degradation of TN-T and its association with PMI. Kumar et al.29 discovered that the degradation of TN-T in cardiac tissue samples with appreciate to time in deaths of mycardical infraction, burn, electrocution, handle, poisoning and asphyxia. besides the fact that children, in their latest analyze, the postmortem TN-T expression in cardiac blood each in manage group and experimental community have been stable and regression analysis effects revealed no huge relationship between TN-T and PMI. There are varied possible motives for discrepant results between old examine and current study, such as the cost of fragmentation of TN-T in diverse samples, the reason for demise, temperature, and so on13,14,15,sixteen,17,18,29.

Our statistics in present examine indicated that the postmortem changes of VEGF both in handle and experimental skilled the process of descending then ascending and particularly in experimental agencies that the the levels of VEGF started to boost after 12 h PMI and diminished with PMI as much as forty eight h, then extended linearly with PMI up to 168 h; and effects of old studies27,30 additionally confirmed that the time-course of VEGF expression with tissue-certain changes. so that the regression analysis results published no giant relationship between VEGF and PMI. in response to the existing data, the mannequin discover the non-linear relationship between VEGF and PMI can also be built in extra look at with a purpose to provide a reference for the PMI estimation in forensic identification.

Regression evaluation effects published no enormous relationship between HIF -1α and PMI inside the 168 h after loss of life each in control and experimental. In their latest look at, they discovered that the postmortem adjustments of HIF-1α became consistent with previous analyze that HIF-1α expression was regularly decreased four–5 days after death28; despite the fact, HIF-1α protein expression as a brand new marker for PMI estimation in human gingival tissue become proven in outdated analyze and the effects of the analyze counseled HIF1α is a promising biomarker for distinguishing deaths that have took place within 1 week from those who befell more than 1 week in the past; so that a great deal greater lengthy-time period statement of HIF-1α expression in their extra study will support us to clarify the difference between outdated analyze and their present look at.

Regression evaluation outcomes printed a significant relationship between VEGF/HIF-1α and PMI whereas no big relationships between VEGF/TN-T and PMI, HIF-1α/TN-T and PMI in experimental neighborhood. These facts indicated that the ratio of VEGF/HIF-1α appears to be a effective system of estimating the PMI up to 168 h in forensic identification. but regression evaluation consequences published no enormous relationships between VEGF/TN-T and PMI, HIF-1α/TN-T and PMI, VEGF/HIF-1α and PMI.

based on the above founding, they extra analyzed the affiliation between TN-T, VEGF, HIF-1α, VEGF/TN-T, HIF-1α/TN-T, VEGF/HIF-1α and PMI through the use of linear regression evaluation and the outcomes published a big relationship between VEGF/HIF-1α and PMI regardless of cause of loss of life. This discovering is an encouraging discovery in reality instantly that VEGF/HIF-1α guarantees to be a biomarker to estimate PMI inspite of reason for death; besides the fact that children, this discovering needs to be demonstrated with the aid of larger pattern in further look at.

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