Search Results - "Dominic"

Are acquired cystic kidney disease and autosomal dominant polycystic kidney disease risk factors for renal cell carcinoma in kidney transplant patients? by Behzad Einollahi

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The expression of dominant negative TCF7L2 in pancreatic beta cells during the embryonic stage causes impaired glucose homeostasis by Weijuan Shao, Xiaoquan Xiong, Wilfred Ip, Fenghao Xu, Zhuolun Song, Kejing Zeng, Marcela Hernandez, Tao Liang, Jianping Weng, Herbert Gaisano, M. Cristina Nostro, Tianru Jin

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A rare mutation causing autosomal dominant STAT1 deficiency in a South African multiplex kindred with disseminated BCG infection by Leonore Greybe, Daniel Leung, Nicole Wieselthaler, David M le Roux, Koon Wing Chan, Yu Lung Lau, Brian Eley

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Urine-sample-derived human induced pluripotent stem cells as a model to study PCSK9-mediated autosomal dominant hypercholesterolemia by Karim Si-Tayeb, Salam Idriss, Benoite Champon, Amandine Caillaud, Matthieu Pichelin, Lucie Arnaud, Patricia Lemarchand, Cédric Le May, Kazem Zibara, Bertrand Cariou

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Impaired inflammatory pain and thermal hyperalgesia in mice expressing neuron-specific dominant negative mitogen activated protein kinase kinase (MEK) by Kaplan David, Adwanikar Hita, Hu Hui-Juan, Karim Farzana, Gereau Robert W

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Differential genome-wide gene expression profiling of bovine largest and second-largest follicles: identification of genes associated with growth of dominant follicles by Takahashi Toru, Hosoe Misa, Ushizawa Koichi, Hayashi Ken-Go

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Different clinical features in Malawian outpatients presenting with COVID-19 prior to and during Omicron variant dominance: A prospective observational study by Marah G. Chibwana, Herbert W. Thole, Cat Anscombe, Philip M. Ashton, Edward Green, Kayla G. Barnes, Jen Cornick, Ann Turner, Desiree Witte, Sharon Nthala, Chikondi Thom, Felistas Kanyandula, Anna Ainani, Natasha Mtike, Hope Tambala, Veronica N'goma, Dorah Mwafulirwa, Erick Asima, Ben Morton, Markus Gmeiner, Zaziwe Gundah, Gift Kawalazira, Neil French, Nicholas Feasey, Robert S. Heyderman, Todd D. Swarthout, Kondwani C. Jambo

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Altered Serotonin 2A (5-HT2A) Receptor Signaling Underlies Mild TBI-Elicited Deficits in Social Dominance by Sean M. Collins, Christopher J. O'Connell, Evan L. Reeder, Sophia V. Norman, Kainat Lungani, Poornima Gopalan, Gary A. Gudelsky, Gary A. Gudelsky, Matthew J. Robson, Matthew J. Robson

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Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib by McDonald Jay M, Reddy Vishnu, Makris Christopher, Dale Janet K, Zheng Lixin, Atkinson T Prescott, Pan George, Bi Lilia L, Siegel Richard M, Puck Jennifer M, Lenardo Michael J, Straus Stephen E

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Treatment of autosomal dominant retinitis pigmentosa caused by RHO-P23H mutation with high-fidelity Cas13X in mice by Zixiang Yan, Yuqin Yao, Luyao Li, Lingqiong Cai, Haiwei Zhang, Shenghai Zhang, Qingquan Xiao, Xing Wang, Erwei Zuo, Chunlong Xu, Jihong Wu, Hui Yang

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Multicentric papillary and chromophobe renal cell carcinomas in a patient with autosomal dominant polycystic kidney disease: Report of a rare case by Nibedita Sahoo, Susama Patra, Swagatika Senapati, Tushar S Mishra

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A Novel De Novo Dominant Mutation in GJB2 Gene Associated with a Sporadic Case of Nonsyndromic Sensorineural Hearing Loss. by Habib Onsori, Mohammad Rahmati, Davood Fazli

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Trunk, Mass Grasp, Knee, and Hip Muscle Performance in CrossFit Participants: Reference Values According to Participants' Sex and Limb Dominance by Ana Luiza R Rodrigues, Renan A. Resende, Livia S. Pogetti, Thiago R. T. Santos, Henrique M. P. Faria, Mauro H. Chagas, Juliana M Ocarino

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Dominant optic atrophy in Denmark - report of 15 novel mutations in <it>OPA1</it>, using a strategy with a detection rate of 90% by Almind Gitte J, Ek Jakob, Rosenberg Thomas, Eiberg Hans, Larsen Michael, LuCamp LuCamp, Brøndum-Nielsen Karen, Grønskov Karen

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Hip adduction and abduction strength profiles in elite and sub-elite female soccer players according to players level and leg limb-dominance by Eloy Jaenada-Carrilero, Juan Vicente-Mampel, Luis Baraja-Vegas, Kristian Thorborg, Eloína Valero-Merlos, Paula Blanco-Gímenez, Pedro Gargallo, Iker J. Bautista

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Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reports by Margareta Fistrek Prlic, Sanda Huljev Frkovic, Sanda Huljev Frkovic, Bodo Beck, Ivana Tonkovic Durisevic, Stela Bulimbasic, Stela Bulimbasic, Marijana Coric, Marijana Coric, Lovro Lamot, Lovro Lamot, Ema Ivandic, Ivana Vukovic Brinar, Ivana Vukovic Brinar

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Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption by Christoph Jüschke, Thomas Klopstock, Claudia B. Catarino, Marta Owczarek-Lipska, Bernd Wissinger, John Neidhardt

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Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles by Fauvert Delphine, Brun-Heath Isabelle, Lia-Baldin, Bellazi Linda, Taillandier Agnès, Serre Jean-Louis, de Mazancourt Philippe, Mornet Etienne

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In-depth analysis of the medical supply for indigenous people in North-Eastern Colombia: a dominance of infectious diseases and only insufficient therapeutic options by Hannah Bauer, Hagen Frickmann, Gustavo Concha, Lothar Kreienbrock, Maria Hartmann, Philipp Warnke, Ralf Matthias Hagen, Ernst Molitor, Achim Hoerauf, Simone Kann

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Identification of PI3K-AKT signaling as the dominant altered pathway in intestinal type ampullary cancers through whole-exome sequencing by Niraj Kumari, Rajneesh K. Singh, Shravan K. Mishra, Narendra Krishnani, Samir Mohindra, Raghvendra L.

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