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

A clinical and genotype-phenotype analysis of MACF1 variants

MACF1变异体的临床和基因型-表型分析

Dekker, Jordy; Schot, Rachel; Aldinger, Kimberly A; Everman, David B; Washington, Camerun; Jones, Julie R; Sullivan, Jennifer A; Spillmann, Rebecca C; Shashi, Vandana; Vitobello, Antonio; Denommé-Pichon, Anne-Sophie; Mosca-Boidron, Anne-Laure; Perrin, Laurence; Auvin, Stéphane; Zaki, Maha S; Gleeson, Joseph G; Meave, Naomi; Wallace, Cassidy; Nambot, Sophie; Delanne, Julian; Ruggiero, Sarah M; Helbig, Ingo; Fitzgerald, Mark P; Leventer, Richard J; Grange, Dorothy K; Argilli, Emanuela; Sherr, Elliott H; Prakash, Supraja; Neilson, Derek E; Nicita, Francesco; Sferra, Antonella; Bertini, Enrico S; Aiello, Chiara; Brockmann, Knut; Kuranov, Alexander B; Kaulfuss, Silke; Basit, Sulman; Alluqmani, Majed; Almatrafi, Ahmad; Friedman, Jan M; Guimond, Colleen; Mohammed, Faruq; Sharma, Pooja; Goel, Divya; Wirth, Thomas; Anheim, Mathieu; Bahena, Paulina; Koparir, Asuman; Kolokotronis, Konstantinos; Vona, Barbara; Haaf, Thomas; Kunstmann, Erdmute; Maroofian, Reza; Sczakiel, Henrike L; Boschann, Felix; Misra-Isrie, Mala; Louie, Raymond J; Stolerman, Elliot S; Sanchez-Lara, Pedro A; Mergler, Sandra; Oegema, Renske; Zarate, Yuri A; Kariminejad, Ariana; Tajsharghi, Homa; Zeidler, Shimriet; Kievit, Anneke J A; Bouman, Arjan; Cappuccio, Gerarda; Brunetti-Pierri, Nicola; Stuurman, Kyra E; Swols, Dayna Morel; Tekin, Mustafa; Upadia, Jariya; Martin, Donna M; Craven, Daniel; Hiatt, Susan M; van de Pol, Laura A; D'Arco, Felice; Margot, Henri; Wilke, Martina; Yousefi, Soheil; Barakat, Tahsin Stefan; van Veghel-Plandsoen, Monique M; Aronica, Eleonora; Anink, Jasper; Rogers, Stephen L; Slep, Kevin C; Doherty, Dan; Dobyns, William B; Mancini, Grazia M S

Medicarpin confers powdery mildew resistance in Medicago truncatula and activates the salicylic acid signalling pathway

紫花苜蓿素赋予蒺藜苜蓿抗白粉病能力并激活水杨酸信号通路

Arunima Gupta, Pallavi Awasthi, Neha Sharma, Sajiya Parveen, Ravi P Vats, Nirpendra Singh, Yashwant Kumar, Atul Goel, Divya Chandran

Maintenance of increased bone mass after PTH withdrawal by sequential medicarpin treatment via augmentation of cAMP-PKA pathway

通过增强 cAMP-PKA 通路,连续使用美卡平治疗来维持 PTH 停药后增加的骨量

Kriti Sharma, Pallavi Awasthi, Ravi Prakash, Sonu Khanka, Ranju Bajpai, Amogh A Sahasrabuddhe, Atul Goel, Divya Singh

Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.

印度人群共济失调的遗传学:来自常用基因筛查工具的综合见解

Sharma Pooja, Sonakar Akhilesh Kumar, Tyagi Nishu, Suroliya Varun, Kumar Manish, Kutum Rintu, Asokchandran Vivekananda, Ambawat Sakshi, Shamim Uzma, Anand Avni, Ahmad Ishtaq, Shakya Sunil, Uppili Bharathram, Mathur Aradhana, Parveen Shaista, Jain Shweta, Singh Jyotsna, Seth Malika, Zahra Sana, Joshi Aditi, Goel Divya, Sahni Shweta, Kamai Asangla, Wadhwa Saruchi, Murali Aparna, Saifi Sheeba, Chowdhury Debashish, Pandey Sanjay, Anand Kuljeet Singh, Narasimhan Ranganathan Lakshmi, Laskar Sanghamitra, Kushwaha Suman, Kumar Mukesh, Shaji Cheruvallill Velayudhan, Srivastava Madakasira Vasantha Padma, Srivastava Achal K, Faruq Mohammed

Co-morbid conditions in COVID-19 patients in Uttarakhand state of India

印度北阿坎德邦新冠肺炎患者的合并症

Goel, Divya; Kumar, Sudhir

Cystic adrenal lesions: A report of five cases

肾上腺囊性病变:五例报告

Goel, Divya; Enny, Loreno; Rana, Chanchal; Ramakant, Pooja; Singh, Kulranjan; Babu, Suresh; Mishra, Anand

Primary squamous cell carcinoma, breast: A challenging diagnosis

原发性乳腺鳞状细胞癌:一项具有挑战性的诊断

Goel, Divya; Rana, Chanchal; Babu, Suresh; Ramakant, Pooja

Hereditary Spastic Paraplegia with Mental Impairment, Thin Corpus Callosum and Amyotrophy: A Road Map to SPG11 Contributors

遗传性痉挛性截瘫伴智力障碍、胼胝体变薄和肌萎缩:SPG11贡献者的路线图

Goel, Divya; Sharma, C M; Kumawat, B L

Clinical and functional outcome of modified Quad surgery in adult obstetric brachial plexus injury patients: Case reports

改良型四肢截骨术治疗成人产科臂丛神经损伤患者的临床和功能结果:病例报告

Nath, Rahul K; Goel, Divya; Somasundaram, Chandra

Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population

脊髓小脑性共济失调10型(SCA10):突变分析和基于常见单倍型的推断表明其在印度人群中较为罕见

Goel, Divya; Suroliya, Varun; Shamim, Uzma; Mathur, Aradhna; Faruq, Mohammed