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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 13, 2024
First-Line Nivolumab Plus Relatlimab Versus Nivolumab Plus Ipilimumab in Advanced Melanoma: An Indirect Treatment Comparison Using RELATIVITY-047 and CheckMate 067 Trial DataGeorgina V Long, Evan J Lipson, F Stephen Hodi, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 11, 2025
The humanistic burden of focal segmental glomerulosclerosis on patients and care-partners in the United StatesJustyna Szklarzewicz, Ute Floege, Daniel Gallego, et al.
Biological Psychiatry|January 1, 2020
Erbin in Amygdala Parvalbumin-Positive Neurons Modulates Anxiety-like BehaviorsZheng-Yi Luo, Lang Huang, Song Lin, et al.
Trends in Molecular Medicine|September 4, 2025
Clinical gene therapy restores hearing: a paradigm shiftShuang Han, Ziting Chen, Daqi Wang, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 8, 2011
Two unusual cases of intractable hyperthyroidism responsive to octreotide: Munchausen syndrome or not?Jian-Min Liu, Li-Qun Gu, Lin Zhao, et al.
Clinical Lymphoma, Myeloma & Leukemia|August 1, 2025
Indirect Comparison of Linvoseltamab Versus Teclistamab for the Treatment of Triple-Class Exposed Relapsed/Refractory Multiple MyelomaHans C Lee, Naresh Bumma, Joshua Richter, et al.
Nature|December 21, 2017
Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agentsXue Gao, Yong Tao, Veronica Lamas, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2024
Inverse regulation of SOS1 and HKT1 protein localization and stability by SOS3/CBL4 in Arabidopsis thalianaFrancisco Gámez-Arjona, Hee Jin Park, Elena García, et al.
Lancet (London, England)|January 27, 2024
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trialJun Lv, Hui Wang, Xiaoting Cheng, et al.
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