Disruption of Sex-Linked <i>Sox3</i> Causes ZW Female-to-Male Sex Reversal in the Japanese Frog <i>Glandirana rugosa</i> by Ikuo Miura, Yoshinori Hasegawa, Michihiko Ito, Tariq Ezaz, Mitsuaki Ogata

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Loss of heterozygosity of CYP2D6 enhances the sensitivity of hepatocellular carcinomas to talazoparibResearch in context by Xiaonan Zhang, Natallia Rameika, Lei Zhong, Verónica Rendo, Margus Veanes, Snehangshu Kundu, Sandro Nuciforo, Jordan Dupuis, Muhammad Al Azhar, Ioanna Tsiara, Pauline Seeburger, Shahed Al Nassralla, Viktor Ljungström, Richard Svensson, Ivaylo Stoimenov, Per Artursson, Markus H. Heim, Daniel Globisch, Tobias Sjöblom

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Gain-of-Function and Loss-of-Function Mutations in the RyR2-Expressing Gene Are Responsible for the CPVT1-Related Arrhythmogenic Activities in the Heart by Roshan Paudel, Mohsin Saleet Jafri, Aman Ullah

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Molecular mechanisms linking loss of TDP-43 function to amyotrophic lateral sclerosis/frontotemporal dementia-related genes by Yuka Koike

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Specific analysis of SOD1 enzymatic activity in CSF from ALS patients with and without SOD1 mutations by Laura Leykam, Karin M.E. Forsberg, Ulrika Nordström, Karin Hjertkvist, Agneta Öberg, Eva Jonsson, Peter M. Andersen, Stefan L. Marklund, Per Zetterström

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Case report: A novel de novo germline loss-of-function mutation in the STAT1 transactivation domain in two Chinese siblings, with the elder sibling presenting with multifocal Bacil... by Qin Ying Lim, Qin Ying Lim, Daniel Leung, Crystal K. Lam, Xingtian Yang, Kai N. Cheong, Kai N. Cheong, Andrew K. H. Yik, Jing Yang, Koon-Wing Chan, Pamela P. W. Lee, Pamela P. W. Lee, Pamela P. W. Lee, Pamela P. W. Lee, Miyuki Tsumura, Elaine Y. L. Au, Jaime S. Rosa Duque, Jaime S. Rosa Duque, Jaime S. Rosa Duque, Satoshi Okada, Yu Lung Lau, Yu Lung Lau, Yu Lung Lau

Subjects: “…STAT1 loss-of-function…”
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Polyphenol-Protein Complexes and Their Consequences for the Redox Activity, Structure and Function of Honey. A Current View and New Hypothesis – a Review by Brudzynski Katrina, Maldonado-Alvarez Liset

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Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia by Alessandra P. Porretta, Etienne Pruvot, Zahurul A. Bhuiyan

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Functional characterization of novel compound heterozygous missense SLC5A5 gene variants causing congenital dyshormonogenic hypothyroidism by Gerardo Hernán Carro, Gerardo Hernán Carro, Mariano Martín, Mariano Martín, Sofía Savy, Sofía Savy, Victoria Peyret, Victoria Peyret, Romina Celeste Geysels, Romina Celeste Geysels, Francisco Andrés Montes, Francisco Andrés Montes, Carlos Eduardo Bernal Barquero, Carlos Eduardo Bernal Barquero, Valentina Ricci, Valentina Ricci, María Eugenia Masnata, María Eugenia Masnata, Ana María Masini-Repiso, Ana María Masini-Repiso, Patricia Papendieck, Patricia Papendieck, Mariana Lorena Tellechea, Mariana Lorena Tellechea, Ana Elena Chiesa, Ana Elena Chiesa, Juan Pablo Nicola, Juan Pablo Nicola

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