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Pediatric Nephrology (Berlin, Germany)|September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two familiesDalia Pantel, Nils D Mertens, Ronen Schneider, et al.
Cell Death and Differentiation|February 25, 2012
Pivotal role of the RanBP9-cofilin pathway in Aβ-induced apoptosis and neurodegenerationJ A Woo, A R Jung, M K Lakshmana, et al.
International Journal of Obesity (2005)|February 21, 2017
Effect of an obesity prevention program focused on motivating environments in childhood: a school-based prospective studyY Yang, B Kang, E Y Lee, et al.
Frontiers in Genetics|October 17, 2022
<i>CFAP300</i> mutation causing primary ciliary dyskinesia in FinlandRüdiger Schultz, Varpu Elenius, Mahmoud R Fassad, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 22, 2023
Best practices in epidermal growth factor receptor T790M testing for advanced non-small-cell lung cancer in Hong KongJ S F Nyaw, K M Cheung, F Hioe, et al.
Physical Review Letters|July 9, 2016
Screening Nuclear Field Fluctuations in Quantum Dots for Indistinguishable Photon GenerationR N E Malein, T S Santana, J M Zajac, et al.
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