日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy

印度扩张型心肌病患者β-MYH7基因的新突变

Rani, Deepa Selvi; Vijaya Kumar, Archana; Nallari, Pratibha; Sampathkumar, Katakam; Dhandapany, Perundurai S; Narasimhan, Calambur; Rathinavel, Andiappan; Thangaraj, Kumarasamy

A Rare Case of Dysmorphism with Duplication in Chromosome 22

22号染色体重复导致的罕见畸形病例

Deepika, Mln; Tella, Sunitha; Avvari, Srilekha; Pratibha, Nallari; Ananthapur, Venkateshwari

Epidermolysis Bullosa: A Report of Three Cases with Novel Heterozygous Deletions in PLEC and Homozygous Non sense Mutations in COL7A1 Genes

大疱性表皮松解症:PLEC基因中新型杂合缺失和COL7A1基因中纯合无义突变的三例病例报告

Tella, Sunitha; Sultana, Shehnaz; Madireddy, Sujatha; Nallari, Pratibha; Ananthapur, Venkateshwari

BRIP1/FANCJ Mutation Analysis in a Family with History of Male and Female Breast Cancer in India

印度一个有男性和女性乳腺癌病史的家族中BRIP1/FANCJ基因突变分析

Venkateshwari, Ananthapur; Clark, David Wayne; Nallari, Pratibha; Vinod, Cingeetham; Kumarasamy, Thangaraj; Reddy, Goverdhan; Jyothy, Akka; Kumar, Malladi Vijay; Ramaiyer, Raghuraman; Palle, Komaraiah

Significant Association of Interleukin4 Intron 3 VNTR Polymorphism with Susceptibility to Gastric Cancer in a South Indian Population from Telangana

在印度南部特伦甘纳邦人群中,白细胞介素4内含子3 VNTR多态性与胃癌易感性存在显著关联

Bhayal, Amar Chand; Krishnaveni, Devulapalli; Rao, Kondadasula Pandu Ranga; Kumar, Adi Rakesh; Jyothy, Akka; Nallari, Pratibha; Venkateshwari, Ananthapur

Evaluation of TNF-α, IL-10 and IL-6 Cytokine Production and Their Correlation with Genotype Variants amongst Tuberculosis Patients and Their Household Contacts

结核病患者及其家庭接触者中TNF-α、IL-10和IL-6细胞因子产生情况的评估及其与基因型变异的相关性

Joshi, Lavanya; Ponnana, Meenakshi; Sivangala, Ramya; Chelluri, Lakshmi Kiran; Nallari, Prathiba; Penmetsa, Sitaramaraju; Valluri, Vijayalakshmi; Gaddam, Sumanlatha

Mutational analysis of SCN5A gene in long QT syndrome

长QT综合征中SCN5A基因的突变分析

Qureshi, Sameera Fatima; Ali, Altaf; John, Princy; Jadhav, Amol P; Venkateshwari, Ananthapur; Rao, Hygriv; Jayakrishnan, M P; Narasimhan, Calambur; Shenthar, Jayaprakash; Thangaraj, Kumarasamy; Nallari, Pratibha

Interleukin 10 gene promoter polymorphisms in women with early-onset pre-eclampsia

早发型子痫前期女性的白细胞介素 10 基因启动子多态性

Sowmya, S; Sri Manjari, K; Ramaiah, A; Sunitha, T; Nallari, P; Jyothy, A; Venkateshwari, A

Haplotype analyses of DNA repair gene polymorphisms and their role in ulcerative colitis

DNA修复基因多态性的单倍型分析及其在溃疡性结肠炎中的作用

Bardia, Avinash; Tiwari, Santosh K; Vishwakarma, Sandeep K; Habeeb, Md Aejaz; Nallari, Pratibha; Sultana, Shaik A; Pasha, Shaik A; Reddy, Yugandhar P; Khan, Aleem A

A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM)

印度一个患有扩张型心肌病 (FDCM) 的多代家族中发现肌钙蛋白 T (cTnT) 基因的新型精氨酸到色氨酸 (R144W) 突变

Rani, Deepa Selvi; Dhandapany, Perundurai S; Nallari, Pratibha; Narasimhan, Calambur; Thangaraj, Kumarasamy