Results 201 to 210 of about 531,866 (340)

Co‐Opting MBNL‐Dependent Alternative Splicing Cassette Exons to Control Gene Therapy in Myotonic Dystrophy

Annals of Neurology, EarlyView.
Objective Myotonic dystrophy type 1 (DM1) is a highly variable, multisystemic genetic disorder caused by a CTG repeat expansion in the 3′ untranslated region of DMPK. Toxicity is exerted by repeat‐containing DMPK transcripts that sequester muscleblind‐like (MBNL) proteins and lead to deleterious yet predictable changes in alternative splicing.
Samuel T. Carrell, Ellie M. Carrell, Ryan Giovenco, Beverly L. Davidson   +3 more
wiley   +1 more source

MTHFR allele and one-carbon metabolic profile predict severity of COVID-19. [PDF]

Proc Natl Acad Sci U S A
Petrova B, Syphurs C, Culhane AJ, Chen J, Chen E, Cotsapas C, Esserman D, Montgomery RR, Kleinstein SH, Smolen KK, Mendez K, IMPACC Network, Lasky-Su J, Steen H, Levy O, Diray-Arce J, Kanarek N.   +16 more
europepmc   +1 more source

Effect of dietary of lysine and methionine on performance of vanaraja breeder chicks [PDF]

, 2007
A.K. Panda, S.V. Rama Rao, M.V.L.N. Raju, G. Shyam Sunder, M. R. Reddy   +4 more
openalex  

ACYL ADENYLATES: THE INTERACTION OF ADENOSINE TRIPHOSPHATE AND l-METHIONINE

, 1956
Paul Berg, With the technical assistance of Georgia Newton   +1 more
openalex   +1 more source

Non‐Synaptic Function and Localization of Syntaxin‐Binding Protein 1 in a Mouse Model of STXBP1‐Related Epileptic Encephalopathy

Annals of Neurology, EarlyView.
Objective De novo mutations in the syntaxin‐binding protein 1 (STXBP1), encoded by STXBP1, are among the most prevalent causes of variable neurodevelopmental disorders, including epileptic encephalopathy, developmental delay, and movement disorders.
Tao Yang, Rajat Banerjee, Yamei Deng, Sheetal Jahagirdar1, Alexey I. Nesvizhskii, Michael D. Uhler, Jack M. Parent, Yu Wang   +7 more
wiley   +1 more source

The Double-Edged Nature of Methyl Donors in Cancer Development from Prevention to Progression. [PDF]

Int J Mol Sci
Pan D, Wang S, Sun G.
europepmc   +1 more source

Impact of Methionine and Tryptophan Supplementation on Silk Gland Weight and Tissue Somatic Index in Eri Silkworm (Samia ricini Donovan)

Arup Kumar Hazarika, Prety Rekha Narzary, Monimala Saikia, Hemanta Saikia, Shilpa Saikia, Amlanjyoti Rajkhowa, Bidisha Kashyap, Arsha A Sangma, Shilpi K. Saikia, S.D. Borah, R.R. Saikia   +10 more
openalex   +1 more source

Identification and analysis of the promoter region of the human methionine sulphoxide reductase A gene [PDF]

, 2005
Antonella De Luca, Paolo Sacchetta, Carmine Di Ilio, Bartolo Favaloro   +3 more
openalex   +1 more source

The Phenotypic Spectrum of Sporadic Creutzfeldt‐Jakob Disease Cortical Subtype

Annals of Neurology, EarlyView.
Objective The objective of this study was to characterize the phenotypic spectrum of the rare sporadic Creutzfeldt‐Jakob disease cortical subtype (sCJDMM/MV2C) in a large multicentric autopsy cohort. Methods We evaluated clinical histories, biofluid markers, brain diffusion‐weighted (DW)‐magnetic resonance imaging (MRI), and electroencephalogram (EEG ...
Simone Baiardi, Claudia Marina Vargiu, Brian S. Appleby, Marcelo Barria, Giuseppe Mario Bentivenga, Ignazio Calì, Benedetta Carlà, Mark Cohen, Armin Giese, Jochen Herms, Aino‐Minerva Kortelainen, Anna Ladogana, Angela Mammana, Diane Ritchie, Otto Windl, Sabina Capellari, Piero Parchi   +16 more
wiley   +1 more source

Methionine deficiency causes spermatogonial apoptosis via oxidative stress and DNA damage response pathway. [PDF]

Biol Res
Wang W, Ruan Y, Ting G.
europepmc   +1 more source