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

Samaashraya: An Initiative to Address the COVID-19 and Pandemic-Related Psychosocial and Mental Health Concerns in India

Samaashraya:一项旨在解决印度新冠疫情及相关社会心理和心理健康问题的倡议

Sadh, Kamaldeep; Bhasker Reddy P; George, Sobin; Christopher, Allen Daniel; Mosale, Abhineeth; Gupta, Nidhi; Raghunath M; Devaki, N S; Ravindran, Swati; Ibrahim, Ferose Azeez; Nirisha, P Lakshmi; Malathesh, Barikar C; Dinakaran, Damodharan; Goyal, Ajay Kumar; Manikappa, Sanjeev Kumar; Christy, Jayakumar; Roopesh, Bangalore N; Sekar, Kasi; Kumar, Channaveerachari Naveen

Natural antioxidant activity of commonly consumed plant foods in India: effect of domestic processing

印度常见食用植物性食物的天然抗氧化活性:家庭加工的影响

Sreeramulu, D; Reddy, C V K; Chauhan, Anitha; Balakrishna, N; Raghunath, M

Ankle-Brachial index by oscillometry: A very useful method to assess peripheral arterial disease in diabetes

踝臂指数示波法测定:一种评估糖尿病周围动脉疾病的有效方法

Premanath, M; Raghunath, M

The Scar-in-a-Jar: studying potential antifibrotic compounds from the epigenetic to extracellular level in a single well.

罐中疤痕:在单个孔中从表观遗传到细胞外水平研究潜在的抗纤维化化合物

Chen C Z C, Peng Y X, Wang Z B, Fish P V, Kaar J L, Koepsel R R, Russell A J, Lareu R R, Raghunath M

The Tight skin mouse: demonstration of mutant fibrillin-1 production and assembly into abnormal microfibrils

紧肤小鼠:突变型纤连蛋白-1的产生及其组装成异常微纤维的证明

Kielty, C M; Raghunath, M; Siracusa, L D; Sherratt, M J; Peters, R; Shuttleworth, C A; Jimenez, S A

A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly

在一个患有先天性挛缩性蜘蛛指(趾)的大家族中,一种罕见的基因分支点突变与纤连蛋白-2的错误剪接有关。

Maslen, C; Babcock, D; Raghunath, M; Steinmann, B

Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndrome

对FBN1基因中366 bp缺失导致的截短型原纤维蛋白进行分析,该缺失可导致马凡综合征。

Raghunath, M; Kielty, C M; Kainulainen, K; Child, A; Peltonen, L; Steinmann, B

Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome

新生儿马凡综合征患者成纤维细胞培养物中原纤维蛋白和核心蛋白聚糖的缺乏

Superti-Furga, A; Raghunath, M; Willems, P J