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

Hemoglobin alpha-like subunit mu is expressed during ontogeny and is elevated in alpha thalassemia

血红蛋白α样亚基μ在个体发育过程中表达,并在α地中海贫血中升高。

Garapati, Kishore; Chavan, Sandip; Bellad, Anikha; Venkataraman, Shilpa; Oglesbee, Devin; Chakraborty, Rana; Wick, Myra J; Girard, Sylvie; Pandey, Akhilesh

A Mass Spectrometry-Based Multiplexed Targeted Assay for Detection of Hemoglobinopathies from Dried Blood Spots

基于质谱的多重靶向检测干血斑中血红蛋白病的方法

Bellad, Anikha; Rangiah, Kannan; Chavan, Sandip; Warade, Jayesh; Das, Barnali; Pandey, Akhilesh

Identification of a rare [(G)γ((A)γδβ)(0)] -thalassemia using tandem mass spectrometry

利用串联质谱法鉴定一种罕见的[(G)γ((A)γδβ)(0)]-地中海贫血

Bellad, Anikha; Rangiah, Kannan; Sathe, Gajanan; Dey, Gourav; Appadorai, Pragalatha Kumar; Lokanatha, Hemalatha; Murthy, Pradeep Rudra; Gowdra, Aruna; Pandey, Akhilesh

Urinary Proteomics for Discovery of Gastric Cancer Biomarkers to Enable Precision Clinical Oncology

尿液蛋白质组学用于发现胃癌生物标志物以实现精准临床肿瘤学

Neha Joshi, Firdous Bhat, Anikha Bellad, Gajanan Sathe, Anu Jain, Sandip Chavan, Ravi Sirdeshmukh, Akhilesh Pandey

Applications of quantitative metabolomics to revolutionize early diagnosis of inborn errors of metabolism in India

定量代谢组学在印度应用于先天性代谢缺陷早期诊断的革命性应用

Chandran, Jisha; Bellad, Anikha; Ramarajan, Madan Gopal; Rangiah, Kannan

A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability

一种新的LINS1截断突变导致常染色体隐性非综合征型智力障碍

Muthusamy, Babylakshmi; Bellad, Anikha; Prasad, Pramada; Bandari, Aravind K; Bhuvanalakshmi, G; Kiragasur, R M; Girimaj, Satish Chandra; Pandey, Akhilesh

KIAA1109 gene mutation in surviving patients with Alkuraya-Kučinskas syndrome: a review of literature

Alkuraya-Kučinskas综合征幸存患者中KIAA1109基因突变:文献综述

Kumar, Kishore; Bellad, Anikha; Prasad, Pramada; Girimaji, Satish Chandra; Muthusamy, Babylakshmi