Explain how the early Church continues the ministry of Jesus as presented in the New
Testament.
7. Explain the issues associated with the Judaizers in the early Church, especially as seen in
the letter to the Galatians.
8. Explain how Verbum Domini understands the relationship between Scripture and culture
The early Church continued the ministry of Jesus as presented in the New Testament by emphasizing his teachings and applying them to their lives. The Church was established shortly after the ascension of Jesus and it consisted of both Jews and Gentiles who followed His teachings. This was a unified fellowship that met together for worship, prayer, teaching from Scripture, fellowship & service (Acts 20:7). Within this context believers were united in their commitment to living out Christ’s commands as outlined in the gospels such as loving God above all else (Matthew 22:37-40) , caring for others (Luke 10:25-37), being humble before God & man(Matthew 5:3-12)
Additionally they sought to spread these gospel message through preaching & evangelism. In fact Jesus had specifically instructed his followers to “go into all nations” so that they could make disciples of all peoples (Matthew 28:19). The early Church set out on this mission with zeal publicly proclaiming Christ\’s good news within their own communities as well travelling far away lands with same purpose in mind(Acts 8:4-8).
Moreover they practiced what they preached engaging in acts of compassion towards those less fortunate than themselves providing food, clothing & shelter when needed along with visiting prisoners & sick people (James 2:15-17). Thus the early Church mirrored much of Jesus\’ ministry through its commitment towards helping those affected by poverty or illness seeking to bring healing & hope within each situation encountered.
In conclusion, through its dedication towards following Christ’s instructions faithfully whilst serving others selflessly the Early Church exemplified much Of what made up our Lord’S own earthly ministry. By doing so it demonstrated how committed discipleship can lead one on a path which benefits both oneself plus society at large thereby bringing glory unto God .
Genes that have genetical variation encode enzymes which metobolize drug, drug transporters, or drug targets. Variation in genes that can predict dose and safety of treatment for different types of cancer patient can have harmful influence on these patients’ treatment(25). For instance, polymorphism where in cytochrome P450 enzymes could cause to metabolite to drug slowly or very fast. So patient give an overdose symptoms or no response to drug by changing the pharmacokinetics of drug metabolism, also it may cause an adverse drug reaction(26). Thereby , forecasting optimal dose of drug , inducing the harmful side effects can be provided by using polymorphism(27). In familial breast cancer, patients shows low survival rate to treatment with tamoxifen that is chemotherapeutic drug because of genetic variation in CYP2D6 that is seen as a poor metabolizer (28). There are some studies abour genetic testing on drug label including test for CYP450 polymorphisms.
Prognosis
Insteaf of using clinicopathologic parameters as a biomarker in biochemical testing for prognosis and selection of therapatic way for cancer patient , Genotyping or gene expression profiling by microarray and protein analysis by mass spectrometry is used for prognostic biomarkers with the understanding of the molecular mechanism of cancer subtypes(29).
Biomarkers can be used alone or with combination of other parameters for classify subgroups according to their risk rate and for leading to therapy decision. For example, tissue microarray analysis with combining molecular and clinical biomarker is more efficient than the clasical clinical parameter for patient who has renal cell carcinoma(30).
Instead of using PCR, fluorescence in situ hybridization, immunohistochemistry, and sequencing for personalized medicine testing, high throughput analyses that consist of microarray, mass spectrometry, second generation sequencing, array comparative genomic hybridization, and high-throughput single nucleotide polymorphism (SNP) analysis were started to use after human genome project . These techniques can analyse numerous target at the same time(31). New technologies improve sesitiveness, speciality, trueness of new b