Evaluation of the Secretor Status of ABO Blood Group Antigens in Saliva using Absorption Inhibition Method [0.03%]
吸收抑制法测定ABO血型唾液分泌型的评价研究
M L Avinash Tejasvi,Jaya Laksmi Bukkya,Pandu Ranga Rao et al.
M L Avinash Tejasvi et al.
Objectives While DNA profiling has become the principal technique for individualization of biological evidences, ABO blood grouping is still a useful test method in the initial stages of crime investigation. Objectives of the study were blo...
CTLA-4 (+49A/G) Polymorphism in Type 1 Diabetes Children of Sudanese Population [0.03%]
苏丹人群1型糖尿病患儿CTLA-4(+49A/G)基因多态性研究
Khalid E Khalid Kheiralla
Khalid E Khalid Kheiralla
Background Type 1 diabetes mellitus (T1DM) is an organ-specific T cell-mediated autoimmune disease, characterized by destruction of pancreatic islets. Cytotoxic lymphocyte antigen-4 ( CTLA-4 ) is a negative regulator of T cell proliferation...
Potential of CRISPR/Cas13 System in Treatment and Diagnosis of COVID-19 [0.03%]
CRISPR/Cas13系统在治疗和诊断新型冠状病毒肺炎中的潜力
Amir Khodavirdipour,Motahareh Piri,Sarvin Jabbari et al.
Amir Khodavirdipour et al.
The novel coronavirus disease 2019 (COVID-19) belongs to coronaviridae families like sarbecovirus (SARS), and causes pyrexia, pertussis, and acute respiratory distress syndrome (ARDS) in major. Started from Wuhan, China, COVID-19 now forced...
Association of Assisted Reproductive Technology Treatments with Imprinting Disorders [0.03%]
辅助生殖技术治疗与表观遗传印记疾病之间的关联性研究
T Kopca,Pinar Tulay
T Kopca
Assisted reproductive technology (ART) is a broad field in infertility that encompasses different types of treatments. These revolutionary treatment methods aimed to aid infertile or subfertile couples. Treatment was expanded exponentially,...
Inconsistency of Karyotyping and Array Comparative Genomic Hybridization (aCGH) in a Mosaic Turner Syndrome Case [0.03%]
染色体核型与基因芯片在嵌合型特纳综合征中的不一致分析
Pinar Tulay,Mahmut Cerkez Ergoren,Ahmet Alkaya et al.
Pinar Tulay et al.
Purpose Turner syndrome is a sex chromosomal aberration where majority of the patients have 45,X karyotype, while several patients are mosaic involving 45,X/46,XX; 46,X,i(Xq); and other variants. Cytogenetic analysis, karyotyping, is consid...
Impact of ERCC2 Gene Polymorphisms on OSCC Susceptibility and Clinical Characteristics [0.03%]
ERCC2基因多态性对口腔鳞癌易感性和临床特征的影响研究
Ml Avinash Tejasvi,Gopal Maragathavalli,Putcha Uday Kumar et al.
Ml Avinash Tejasvi et al.
Background DNA repair systems play an important role in maintaining the integrity of the human genome. Deficiency in the repair capacity due to either mutations or inherited polymorphisms in DNA repair genes may contribute to variations in ...
The Connotation of Variances in the Risk Predictors, Medications, Homocysteine, and Homocysteine Pathway Gene Polymorphisms with CVA/Stroke [0.03%]
风险预测因素、用药种类、同型半胱氨酸及同型半胱氨酸通路基因多态性与脑血管病关联性的内涵研究
Rizwan Masud,Aleem Ul Haq Khan,Aiman Farogh Anjum et al.
Rizwan Masud et al.
Cerebrovascular accidents (CVAs) are vascular multifactorial, multigenic ailments with intricate genetic, environmental risk influences. The present study aimed to establish affiliation of CVAs/stroke with blood parameters, differences in p...
Further Evidence of a Recessive Variant in COL1A1 as an Underlying Cause of Ehlers-Danlos Syndrome: A Report of a Saudi Founder Mutation [0.03%]
COL1A1基因隐性突变导致埃勒斯-丹洛斯综合征进一步证据：沙特始祖突变报告
Ahmad Almatrafi,Jamil A Hashmi,Fatima Fadhli et al.
Ahmad Almatrafi et al.
Ehlers-Danlos syndrome (EDS) is a group of clinically and genetically heterogeneous disorder of soft connective tissues. The hallmark clinical features of the EDS are hyperextensible skin, hypermobile joints, and fragile vessels. It exhibit...
Mahamad Irfanulla Khan,Prashanth Cs,Narasimha Murthy Srinath
Mahamad Irfanulla Khan
Orofacial clefts (OFCs) are the most common congenital birth defects in humans and immediately recognized at birth. The etiology remains complex and poorly understood and seems to result from multiple genetic and environmental factors along...
Praveen Kumar Neela,Anjana Atteeri,Pavan Kumar Mamillapalli et al.
Praveen Kumar Neela et al.
The development of craniofacial complex and dental structures is a complex and delicate process guided by specific genetic mechanisms. Genetic and environmental factors can influence the execution of these mechanisms and result in abnormali...