Thesis
Comparative Study of Human Betaine Homocysteine from Different Patients
A lot of factors found to be related to diseases in one way or another, in the past years many studies showed that there was a risk factor that affects several diseases which is betaine Homocysteine. This study will consider homocysteine level as a factor and a marker for certain types of diseases. This study 75 different patients with different diseases and 40 healthy individuals (control) the current results revealed statistically significant difference among the all studied groups.
Genetic Polymorphism in SCL22A12 Gene Associated with Gout in a Sample of Iraqi Patients
The current study aimed to investigate the molecular defect causing the manifestation of gouty arthritis , the relationship between kidney function and the gout and , study the relationship between white blood cell count and gout in a sample of Iraqi patients .The study included 35 patients suffering from gout during the period from January 2015 to June 2015 at Al- Karamah and Al-Yarmouk teaching hospitals .20 healthy subjects were selected to represent the control group.
Genetic Polymorphism in SCL22A12 Gene Associated with Gout in a Sample of Iraqi Patients
The current study aimed to investigate the molecular defect causing the manifestation of gouty arthritis , the relationship between kidney function and the gout and , study the relationship between white blood cell count and gout in a sample of Iraqi patients .The study included 35 patients suffering from gout during the period from January 2015 to June 2015 at Al- Karamah and Al-Yarmouk teaching hospitals .20 healthy subjects were selected to represent the control group.
Immunophenotypic and IL-17 Genetic Evaluation in Iraqi Patients with Chronic Myeloid Leukemia
This study was designed to shed light on the association between the genetic variations in IL-17A and IL-17F genes, and their levels in chronic myeloid leukemia (CML).Sixty two patients (38 males, and 24 females), with an age range 21 – 73 years old, were diagnosed with chronic myeloid leukemia, and 28 healthy individuals (18 males and 10 females), with an age range 24 – 72 years old, were enrolled in this study.
Biochemical and Histopathollogical Study of Moringa oleifera Extract on the Fertility in Male Mice
This study was designed to find out the effect of Moringa oleifera leaf extracts on fertility of male albino mice. M. oleifera leaf extract was prepared by maceration of 50 gm of M. oleifera leaves with 70%
methanol, then chemical detection of flavonoids, alkaloids, tannins, saponins, glycosides, terpenes and steroids were detected. Isolation of Flavonoid from these extracts. The use of thin layer hromatography
Antitumor and Antioxidant Activity of Different Pelargonium graveolens Crude Leaves Extracts
Pelargonium graveolens is an important medicinal plant which is traditionally used to staunch bleeding, heal wounds, ulcers and skin disorders as well as treat diarrhea and dysentery. The present study was
Effect of Static Magnetic Field on Amylase and Protease Produced by some Fungal isolates using Solid State Fermentation
In this study, the effect of static magnetic field on the production of amylase and protease enzymes using solid state fermentations from five different fungal species Alternaria sp., Aspergillus niger, Fusarium sp., Mucor sp., and Penicillium sp. were investigated. The substrate used for fungi growth was bread only.
Antibacterial and Antimutagenic Effects of Synthetic Histidine
This study was accomplished to determine the Histidine behaviors toward two pathogenic bacteria (Staphylococcus aureus and Escherichia coli) toward exposed to various conditions, as well as to test their susceptibility toward related antibiotics. The method of His measurement in colostrum and natural Iraqi breast milk was modified by transferring the separation column of Amino Acid Analyzer (AAA) to a High Performance Liquid Chromatography (HPLC) that contains a fluorescent detector.
Detection of Mutations in Exon 10 and 13 of ATP7B Gene among Iraqi patients with Wilson Disease
copper metabolism due to mutations in copper transport gene ATP7B resulting in hepatic and neuropsychiatric manifestation. The aim of this study is to investigate the extent to which mutations in gene ATP7B involved in development of WD and assessment of parameters related to copper metabolism in patients with Wilson disease. Accordingly, blood samples were obtained from 35 patients with WD (20 male and 15 female) with a mean age of 9.12 years and age range of 5 – 40 years old Other 10 apparently, healthy individuals were also included.
Genetic Polymorphism in MTHFR and PCO genes associated with the incidence of Polycystic Ovary Syndrome in A sample of Iraqi Women
This study was constructed to investigate Polycystic ovary syndrome (PCOS) related infertility through a biochemical and molecular base associated with single nucleotide polymorphism (SNP) at methylene tetrahydrofolate reductase (MTHFR) gene and Poly cystic ovary (PCO) gene in Polycystic ovary syndrome (PCOS) Patients. The study included fifty blood samples of patients women suffering from Polycystic ovary syndrome (PCOS) during the period from November 2015 to January 2016, collected from Kamal al-Samarrai Hospital in Baghdad governorate.