Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
The Molecular Role of Polyamines in Age-Related Diseases: An Update.
Int J Mol Sci. 2023 Nov 17;24(22):16469. doi: 10.3390/ijms242216469.
Int J Mol Sci. 2023.
PMID: 38003659
Free PMC article.
Review.
Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells.
Rugerio-Martínez CI, Ramos D, Segura-Olvera A, Murillo-Melo NM, Tapia-Guerrero YS, Argüello-García R, Leyva-García N, Hernández-Hernández O, Cisneros B, Suárez-Sánchez R.
Rugerio-Martínez CI, et al. Among authors: murillo melo nm.
Int J Mol Sci. 2022 Oct 6;23(19):11876. doi: 10.3390/ijms231911876.
Int J Mol Sci. 2022.
PMID: 36233175
Free PMC article.
Item in Clipboard
Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.
Magaña JJ, Tapia-Guerrero YS, Velázquez-Pérez L, Cruz-Mariño T, Cerecedo-Zapata CM, Gómez R, Murillo-Melo NM, González-Piña R, Hernández-Hernández O, Cisneros B.
Magaña JJ, et al. Among authors: murillo melo nm.
Int J Clin Exp Med. 2014 Dec 15;7(12):5896-903. eCollection 2014.
Int J Clin Exp Med. 2014.
PMID: 25664129
Free PMC article.
Item in Clipboard
Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1.
Franco-Guerrero AA, Márquez-Quiroz LC, Valadéz-Jiménez VM, Cortés H, Murillo-Melo NM, Muñoz B, Cisneros B, Magaña JJ.
Franco-Guerrero AA, et al. Among authors: murillo melo nm.
Muscle Nerve. 2019 Jul;60(1):90-95. doi: 10.1002/mus.26485. Epub 2019 May 6.
Muscle Nerve. 2019.
PMID: 30994189
Item in Clipboard
A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population.
Faruq M, Magaña JJ, Suroliya V, Narang A, Murillo-Melo NM, Hernández-Hernández O, Srivastava AK, Mukerji M.
Faruq M, et al. Among authors: murillo melo nm.
Ann Hum Genet. 2017 Sep;81(5):197-204. doi: 10.1111/ahg.12200. Epub 2017 Jun 9.
Ann Hum Genet. 2017.
PMID: 28597910
Item in Clipboard
Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Murillo-Melo NM, Márquez-Quiróz LC, Gómez R, Orozco L, Mendoza-Caamal E, Tapia-Guerrero YS, Camacho-Mejorado R, Cortés H, López-Reyes A, Santana C, Noris G, Hernández-Hernández O, Cisneros B, Magaña JJ.
Murillo-Melo NM, et al.
Neuromuscul Disord. 2017 Dec;27(12):1106-1114. doi: 10.1016/j.nmd.2017.09.004. Epub 2017 Sep 21.
Neuromuscul Disord. 2017.
PMID: 29054426
Item in Clipboard
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.
Ballester-Lopez A, Linares-Pardo I, Koehorst E, Núñez-Manchón J, Pintos-Morell G, Coll-Cantí J, Almendrote M, Lucente G, Arbex A, Magaña JJ, Murillo-Melo NM, Lucia A, Monckton DG, Cumming SA, Ramos-Fransi A, Martínez-Piñeiro A, Nogales-Gadea G.
Ballester-Lopez A, et al. Among authors: murillo melo nm.
Genes (Basel). 2020 Jul 7;11(7):757. doi: 10.3390/genes11070757.
Genes (Basel). 2020.
PMID: 32645888
Free PMC article.
Item in Clipboard
Cite
Cite