Mb ascp test prep Samenvattingen, Aantekeningen en Examens

(MB) ASCP TEST PREP COAGULOPATHIES - -Disorder of blood coagulates caused by inherited or acquired defects in coagulation proteins, platelets, or vasculature -Von Wildebrand's Disease, hemophilia, Factor V Leiden DECREASE EXPRESSION - -Methylation of cytosine bases 5' to the gene -siRNAs complementary to the gene transcript INCREASE EXPRESSION - -Histone acetylation close to the gene PRADER-WILLI - -Type of mutation: deletion on chromosome 15 -Gene location: 15q11.2 -Sequence: trans...

Complete BOC: ASCP Test Prep 1) After receiving a 24 hr. urine for quantitative total protein analysis the technician must first: a. subculture the urine for bacteria b. add the appropriate preservative c. screen for albumin using a dipstick d. measure the total volume - d (measure the total volume) 1) Following overnight fasting, hypoglycemia in adults is defined as a glucose of: a. <70 mg/dL (<3.9 mmol/L) b. <60 mg/dL (<3.3mmol/L) c. <55 mg/dL (<3.0mmol/L) d. &l...

(MB) ASCP TEST PREP COAGULOPATHIES - -Disorder of blood coagulates caused by inherited or acquired defects in coagulation proteins, platelets, or vasculature -Von Wildebrand's Disease, hemophilia, Factor V Leiden DECREASE EXPRESSION - -Methylation of cytosine bases 5' to the gene -siRNAs complementary to the gene transcript INCREASE EXPRESSION - -Histone acetylation close to the gene PRADER-WILLI - -Type of mutation: deletion on chromosome 15 -Gene location: 15q11.2 -Sequence: trans...

COAGULOPATHIES - -Disorder of blood coagulates caused by inherited or acquired defects in coagulation proteins, platelets, or vasculature -Von Wildebrand's Disease, hemophilia, Factor V Leiden DECREASE EXPRESSION - -Methylation of cytosine bases 5' to the gene -siRNAs complementary to the gene transcript INCREASE EXPRESSION - -Histone acetylation close to the gene PRADER-WILLI - -Type of mutation: deletion on chromosome 15 -Gene location: 15q11.2 -Sequence: translocation with loss on t...

COAGULOPATHIES - -Disorder of blood coagulates caused by inherited or acquired defects in coagulation proteins, platelets, or vasculature -Von Wildebrand's Disease, hemophilia, Factor V Leiden DECREASE EXPRESSION - -Methylation of cytosine bases 5' to the gene -siRNAs complementary to the gene transcript INCREASE EXPRESSION - -Histone acetylation close to the gene PRADER-WILLI - -Type of mutation: deletion on chromosome 15

ASCP (MB) Final Exam PREP | Questions and Answers (Part III) Complete Solutions, Graded A+ - 2023. What is the major cause of Prader Willi syndrome?: epigenetics; genomic imprinting 8. bDNA can test for what diseases?: HIV Hep - B Hep - C 9. Hybrid capture can test for what diseases?: Cytomegalovirus HPV Hep - B Epstein-barr 10. Probe amplification sequencing can test for what diseases?: familial hypercholesterolemia 11. Nested PCR can test for what diseases?: Synovial carcoma 12. Wha...

COAGULOPATHIES - -Disorder of blood coagulates caused by inherited or acquired defects in coagulation proteins, platelets, or vasculature -Von Wildebrand's Disease, hemophilia, Factor V Leiden DECREASE EXPRESSION - -Methylation of cytosine bases 5' to the gene -siRNAs complementary to the gene transcript INCREASE EXPRESSION - -Histone acetylation close to the gene PRADER-WILLI - -Type of mutation: deletion on chromosome 15