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

Congenital heart disease and folate pathway gene polymorphisms: findings from a North Indian cohort

先天性心脏病与叶酸代谢途径基因多态性:来自北印度人群的研究结果

Kukshal, Prachi; Ahamad, Shadab; Joshi, Radha; Kumar, Ajay; Chellappan, Subramanian

Maternal-Child Blood Group Discordance and Severity of Congenital Heart Disease: Insights From a Tertiary Referral Study

母子血型不一致与先天性心脏病严重程度:来自三级转诊研究的启示

Ahamad, Shadab; Tulsi, Anagha; Sharma, Amita; Kukshal, Prachi

Case-control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India

来自印度北部一家三级儿科心脏中心的先天性心脏病病例对照关联研究

Kukshal, Prachi; Joshi, Radha O; Kumar, Ajay; Ahamad, Shadab; Murthy, Prabhatha Rashmi; Sathe, Yogesh; Manohar, Krishna; Guhathakurta, Soma; Chellappan, Subramanian

Chronologically modified androgen receptor in recurrent castration-resistant prostate cancer and its therapeutic targeting

复发性去势抵抗性前列腺癌中雄激素受体的时间序列改变及其治疗靶向性

Sawant, Mithila; Mahajan, Kiran; Renganathan, Arun; Weimholt, Cody; Luo, Jingqin; Kukshal, Vandna; Jez, Joseph M; Jeon, Myung Sik; Zhang, Bo; Li, Tiandao; Fang, Bin; Luo, Yunting; Lawrence, Nicholas J; Lawrence, Harshani R; Feng, Felix Y; Mahajan, Nupam P

Point mutations that boost aromatic amino acid production and CO2 assimilation in plants

植物中促进芳香族氨基酸生成和二氧化碳同化的点突变

Ryo Yokoyama,Marcos V V de Oliveira,Yuri Takeda-Kimura,Hirofumi Ishihara,Saleh Alseekh,Stéphanie Arrivault,Vandna Kukshal,Joseph M Jez,Mark Stitt,Alisdair R Fernie,Hiroshi A Maeda

Distribution and the evolutionary history of G-protein components in plant and algal lineages

植物和藻类谱系中G蛋白组分的分布和进化史

Mohanasundaram, Boominathan; Dodds, Audrey; Kukshal, Vandna; Jez, Joseph M; Pandey, Sona

Chemical inhibition of the auxin inactivation pathway uncovers the roles of metabolic turnover in auxin homeostasis

生长素失活途径的化学抑制揭示了代谢周转在生长素稳态中的作用

Kosuke Fukui, Kazushi Arai, Yuka Tanaka, Yuki Aoi, Vandna Kukshal, Joseph M Jez, Martin F Kubes, Richard Napier, Yunde Zhao, Hiroyuki Kasahara, Ken-Ichiro Hayashi

Phosphorylation-Dependent Conformations of the Disordered Carboxyl-Terminus Domain in the Epidermal Growth Factor Receptor

表皮生长因子受体中无序羧基末端结构域的磷酸化依赖性构象

Regmi, Raju; Srinivasan, Shwetha; Latham, Andrew P; Kukshal, Vandna; Cui, Weidong; Zhang, Bin; Bose, Ron; Schlau-Cohen, Gabriela S

Association of regulatory variants of dopamine β-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects

多巴胺 β-羟化酶调节变体与精神分裂症患者认知和迟发性运动障碍的关系

Toyanji J Punchaichira, Anirban Mukhopadhyay, Prachi Kukshal, Triptish Bhatia, Smita N Deshpande, B K Thelma

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance

在一个四代精神分裂症家族中发现的多种罕见遗传变异,为揭示该疾病复杂的遗传模式提供了线索。

John, Jibin; Bhattacharyya, Upasana; Yadav, Navneesh; Kukshal, Prachi; Bhatia, Triptish; Nimgaonkar, V L; Deshpande, Smita N; Thelma, B K