Results 251 to 260 of about 2,538,848 (322)

Cloning and expression of the two genes coding for L-serine dehydratase from Peptostreptococcus asaccharolyticus: relationship of the iron-sulfur protein to both L-serine dehydratases from Escherichia coli [PDF]

, 1997
Antje Hofmeister, Susanne Textor, Wolfgang Buckel   +2 more
openalex   +1 more source

Functional Similarities of Protein-Coding Genes in Topologically Associating Domains and Spatially-Proximate Genomic Regions. [PDF]

Genes (Basel), 2022
Zhao C, Liu T, Wang Z.
europepmc   +1 more source

Factors for Rituximab Refractoriness in AQP4‐IgG+ NMOSD: A Cohort Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Neuromyelitis optica spectrum disorder (NMOSD) is a severe autoimmune condition of the central nervous system (CNS), often associated with aquaporin‐4 antibodies (AQP4‐IgG). Rituximab, a CD20+ B‐cell depleting monoclonal antibody, is widely used as first‐line therapy.
Mariano Marrodan, María A. Piedrabuena, María A. Zarate, Sofía Rodríguez Murúa, Ezequiel I. Surace, Mauricio F. Farez, Marcela P. Fiol, María C. Ysrraelit, Jorge Correale   +8 more
wiley   +1 more source

Nucleotide sequence of the gene coding for ribosomal protein S10 from the archaeum Thermoplasma Acidphilum

, 1992
Andréa Cristina Tesch, Friedrich Klink
openalex   +2 more sources

The GC-content at the 5' ends of human protein-coding genes is undergoing mutational decay. [PDF]

Genome Biol
Qiu Y, Kang YM, Korfmann C, Pouyet F, Eckford A, Palazzo AF.   +5 more
europepmc   +1 more source

Loss of the IR region in conifer plastomes: Changes in the selection pressure and substitution rate of protein-coding genes. [PDF]

Ecol Evol, 2022
Ping J, Hao J, Li J, Yang Y, Su Y, Wang T.   +5 more
europepmc   +1 more source

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%), the etiology in most patients remains elusive. Moreover, understanding correlations between clinical manifestations and genetic variants has become increasingly ...
Mirja Thomsen, Fabian Ott, Sebastian Loens, Gamze Kilic‐Berkmen, Ai Huey Tan, Shen‐Yang Lim, Ebba Lohmann, Kaja M. Schröder, Lea Ipsen, Lena A. Nothacker, Linn Welzel, Alexandra S. Rudnik, Frauke Hinrichs, Thorsten Odorfer, Kirsten E. Zeuner, Friederike Schumann, Andrea A. Kühn, Simone Zittel, Marius Moeller, Robert Pfister, Christoph Kamm, Anthony E. Lang, Yi Wen Tay, Ana Luísa de Almeida Marcelino, Marie Vidailhet, Emmanuel Roze, Joel S. Perlmutter, Jeanne S. Feuerstein, Victor S. C. Fung, Florence Chang, Richard L. Barbano, Steven Bellows, Aparna A. Wagle Shukla, Alberto J. Espay, Mark S. LeDoux, Brian D. Berman, Stephen Reich, Andres Deik, Andre Franke, Michael Wittig, Sören Franzenburg, Jens Volkmann, Norbert Brüggemann, H. A. Jinnah, Tobias Bäumer, Christine Klein, Hauke Busch, Katja Lohmann   +47 more
wiley   +1 more source

Expression of the human gene coding for the α-chain of C4b-binding protein, C4BPA, is controlled by an HNF1-dependent hepatic-specific promoter [PDF]

, 1995
Natalia Arenzana, Santiago Rodrı́guez de Córdoba, Javier Rey-Campos   +2 more
openalex   +1 more source

A putative scenario of how de novo protein-coding genes originate in the Saccharomyces cerevisiae lineage. [PDF]

BMC Genomics
Yada T, Taniguchi T.
europepmc   +1 more source

Computational analysis on two putative mitochondrial protein-coding genes from the Emydura subglobosa genome: A functional annotation approach. [PDF]

PLoS One, 2022
Yu M.
europepmc   +1 more source