Baidu
map
筛选条件 共查询到307条结果
排序方式
Momordica charantia nanoparticles potentiate insulin release and modulate antioxidant gene expression in pancreas of diabetic rats

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Green synthesis of nanoparticles with medicinal plants has inherent potential in the management of diabetes mellitus. This study synthesize......

Methyltransferase-like 3 gene (METTL3) expression and prognostic impact in acute myeloid leukemia patients

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background DNA methylation is involved in pathogenesis of acute myeloid leukemia (AML). N6-methyladenosine (m6A) modification of mRNA, mediated by met......

A single-nucleotide polymorphism of IL12A gene (rs582537 A/C/G) and susceptibility to chronic hepatitis B virus infection among Iraqi patients

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

A case-control study (80 patients with chronic hepatitis B virus [HBV] infection and 96 controls) was performed to evaluate the association of an IL12......

Morbidity and mortality of COVID-19 negatively associated with the frequency of consanguineous marriages, an ecologic study

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background: Union between second cousins and closer relatives is called consanguineous marriage. Consanguineous marriage is associated with increased ......

The first combined meta-analytic approach for elucidating the relationship of circulating resistin levels and RETN gene polymorphisms with colorectal and breast cancer

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Evidence suggests that circulating resistin levels are altered in colorectal cancer (CRC) and breast cancer (BC). Again, polymorphisms in r......

Interleukin-4 gene intron 3 VNTR polymorphism in adult acute myeloid leukemia

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background The proliferation of acute myeloid leukemia (AML) blast into the bone marrow microenvironment is controlled by cytokines. Interleukin-4 (IL......

A novel likely pathogenic variant in the H1-4 gene c.139G > C p.(Ala47Pro) associated with Rahman syndrome: a clinical report

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Rahman syndrome (RMNS) is a rare genetic disorder inherited in an autosomal dominant manner caused by a de novo mutation in H1-4 gene. Sinc......

Cerebrospinal fluid biomarkers and genetic factors associated with normal pressure hydrocephalus and Alzheimer's disease: a narrative review

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Normal pressure hydrocephalus is a neurologic disease leading to enlargement of ventricles which is presented with gait and balance disturb......

Validated establishment of anthropometric measurements of mid-face zone in Egyptian healthy preschool-age children: a cross-sectional study

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Objectives To provide normal reference data and identify growth patterns for craniofacial dimensions of a mid-face zone in healthy preschool Egyptian ......

P2X7 1513A/C loss-of-function polymorphism and active tuberculosis disease in a cohort of Egyptian population: a pilot study

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Tuberculosis (TB) is a multifactorial disease, and increasing evidence shows that genetic variants in regulating genes of immune response c......

Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background: Noise, a physical factor in most work environments, has many effects on human health. Exposure to excessive noise can modify the expressio......

Consanguinity in the Chaouia population (Morocco): prevalence, trends, determinants, fertility, and spontaneous abortions

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background One of the aspects that helps to understand the genetic structure of a population throughout its biological history is the description of i......

Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background We present a case of alpha-fucosidosis, a lysosomal storage disorder, from Egypt. The report also includes a brief review of the COVID-19 a......

Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patients

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background Congenital heart disease CHD is a significant cause of mortality and morbidity in children worldwide. Patients with congenital heart diseas......

MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients

期刊: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022; 23 (1)

Background: Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease representing the most prevalent monogenic cause of infant mo......

共307条页码: 1/21页15条/页
Baidu
map
Baidu
map
Baidu
map