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

Epilepsy disease classification: a community effort to enhance the Mondo Disease Ontology

癫痫疾病分类:一项旨在完善 Mondo 疾病本体的社区努力

Vasilevsky, Nicole; Gehrke, Sarah; Mullen, Kathleen; Barua, Subit; Braun, Ian; Brünger, Tobias; Coughlin, Curtis 2nd; Ivaniuk, Alina; Korn, Daniel; Lal, Dennis; Marsh, Stephanie; O'Loughlin, Elaine; Olson, Daniel; Shwetar, Yousif; Sofocleous, Christalena; Vogel-Farley, Vanessa; Grabenstatter, Heidi; Haendel, Melissa; Mungall, Christopher; Toro, Sabrina

Targeted Phototriggered and pH-Responsive Micellar Cancer Drug Delivery System with Real-Time Monitoring through the NSET Mechanism

基于NSET机制的靶向光触发pH响应型胶束抗癌药物递送系统,可实现实时监测

Dyagala, Shalini; Paul, Milan; Das, Sneha; Halder, Sayantan; Biswas, Swati; Saha, Subit K

Construction of a Fluorescence-Based Logic Gate Seeing the Effect of Perchlorate Ions on Hemicyanine Dye-β-Cyclodextrin Complexes to Certify Safe Drinking Water

利用荧光逻辑门研究高氯酸根离子对半菁染料-β-环糊精复合物的影响,以验证饮用水安全

C M, Anusha; Dyagala, Shalini; Choppella, Sairathna; Ravva, Mahesh Kumar; Saha, Subit Kumar

A Novel EP300 Variant in an African American Girl With Global Developmental Delay and Leukemia

一名患有全面发育迟缓和白血病的非裔美国女孩携带一种新型EP300变异株

Barua, Subit; Murty, Vundavalli V; Iglesias, Alejandro; Liao, Jun

Presenting a new fluorescent probe, methyl(10-phenylphenanthren-9-yl)sulfane sensitive to the polarity and rigidity of the microenvironment: applications toward microheterogeneous systems

介绍一种对微环境极性和刚性敏感的新型荧光探针——甲基(10-苯基菲-9-基)硫烷:在微异质系统中的应用

Shalini Dyagala, Nilanjana Mukherjee, Sayantan Halder, Heena Charaya, Mohammed Muzaffar-Ur-Rehman, Sankaranarayanan Murugesan, Shamik Chakraborty, Tanmay Chatterjee, Subit Kumar Saha

Expanding the phenotype of ATP6AP1 deficiency

扩大ATP6AP1缺陷的表型

Barua, Subit; Berger, Sara; Pereira, Elaine M; Jobanputra, Vaidehi

3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities

3q27.1微缺失会导致产前和产后生长受限以及神经发育异常

Barua, Subit; Pereira, Elaine M; Jobanputra, Vaidehi; Anyane-Yeboa, Kwame; Levy, Brynn; Liao, Jun

A treatment-refractory aggressive MDS-MLD with multiple highly complex chromosome 5 intrachromosomal rearrangements: a case report

一例难治性侵袭性骨髓增生异常综合征-骨髓增生异常综合征伴多重高度复杂5号染色体内重排:病例报告

Sasi, Ramakrishnan; Senft, Jamie; Spruill, Michelle; Barua, Subit; Dougaparsad, Sam; Vos, Jeffrey A; Perrotta, Peter L

A novel de novo KDM5C variant in a female with global developmental delay and ataxia: a case report

一例女性患者出现全新KDM5C基因从头突变并伴有全面发育迟缓和共济失调:病例报告

Lippa, Natalie C; Barua, Subit; Aggarwal, Vimla; Pereira, Elaine; Bain, Jennifer M

ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature

ZTTK综合征:15例病例的临床和分子学发现及文献综述

Kushary, Sulagna Tina; Revah-Politi, Anya; Barua, Subit; Ganapathi, Mythily; Accogli, Andrea; Aggarwal, Vimla; Brunetti-Pierri, Nicola; Cappuccio, Gerarda; Capra, Valeria; Fagerberg, Christina R; Gazdagh, Gabriella; Guzman, Edwin; Hadonou, Medard; Harrison, Victoria; Havelund, Kathrine; Iancu, Daniela; Kraus, Alison; Lippa, Natalie C; Mansukhani, Mahesh; McBrian, Danielle; McEntagart, Meriel; Pacio-Míguez, Marta; Palomares-Bralo, María; Pottinger, Carrie; Ruivenkamp, Claudia A L; Sacco, Oliviero; Santen, Gijs W E; Santos-Simarro, Fernando; Scala, Marcello; Short, John; Sørensen, Kristina P; Woods, Christopher G; Anyane Yeboa, Kwame