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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 2
1966 2
1968 1
1970 1
1972 1
1975 1
1976 2
1979 1
1980 1
1981 7
1983 2
1984 3
1985 3
1986 1
1987 3
1988 1
1989 3
1990 5
1993 3
1994 3
1995 3
1996 2
1997 2
1998 5
1999 9
2000 11
2001 19
2002 21
2003 19
2004 27
2005 34
2006 22
2007 34
2008 36
2009 32
2010 45
2011 46
2012 57
2013 63
2014 80
2015 130
2016 141
2017 110
2018 117
2019 149
2020 175
2021 198
2022 147
2023 145
2024 37

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1,698 results

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The following term was not found in PubMed: 20Duce
Page 1
Celia's Encephalopathy (BSCL2-Gene-Related): Current Understanding.
Sánchez-Iglesias S, Fernández-Pombo A, Cobelo-Gómez S, Hermida-Ameijeiras Á, Alarcón-Martínez H, Domingo-Jiménez R, Ruíz Riquelme AI, Requena JR, Araújo-Vilar D. Sánchez-Iglesias S, et al. J Clin Med. 2021 Apr 1;10(7):1435. doi: 10.3390/jcm10071435. J Clin Med. 2021. PMID: 33916074 Free PMC article. Review.
Uniquely, certain variants in BSCL2 can cause both generalized congenital lipodystrophy type 2, upper and/or lower motor neuron diseases, or progressive encephalopathy, with a poor prognosis during childhood. The latter, Celia's encephalopathy, which may or may not be asso …
Uniquely, certain variants in BSCL2 can cause both generalized congenital lipodystrophy type 2, upper and/or lower motor neuron diseases, or …
A murine model of BSCL2-associated Celia's encephalopathy.
Cobelo-Gómez S, Sánchez-Iglesias S, Rábano A, Senra A, Aguiar P, Gómez-Lado N, García-Varela L, Burgueño-García I, Lampón-Fernández L, Fernández-Pombo A, Díaz-López EJ, Prado-Moraña T, San Millán B, Araújo-Vilar D. Cobelo-Gómez S, et al. Neurobiol Dis. 2023 Oct 15;187:106300. doi: 10.1016/j.nbd.2023.106300. Epub 2023 Sep 16. Neurobiol Dis. 2023. PMID: 37717662 Free article.
It is generally caused by the c.985C > T variant in the BSCL2 gene, leading to the skipping of exon 7 and resulting in an aberrant seipin protein (Celia-seipin). To precisely define the temporal evolution and the mechanisms involved in neurodegeneration, lipodystrophy a …
It is generally caused by the c.985C > T variant in the BSCL2 gene, leading to the skipping of exon 7 and resulting in an aberrant seipin …
Ton motor complexes.
Ratliff AC, Buchanan SK, Celia H. Ratliff AC, et al. Curr Opin Struct Biol. 2021 Apr;67:95-100. doi: 10.1016/j.sbi.2020.09.014. Epub 2020 Nov 3. Curr Opin Struct Biol. 2021. PMID: 33157479 Free PMC article. Review.
The Ton Motor.
Ratliff AC, Buchanan SK, Celia H. Ratliff AC, et al. Front Microbiol. 2022 Apr 7;13:852955. doi: 10.3389/fmicb.2022.852955. eCollection 2022. Front Microbiol. 2022. PMID: 35464957 Free PMC article. Review.
Presentación.
Shamah Levy T, Barrientos Gutiérrez T, Alpuche Aranda CM. Shamah Levy T, et al. Salud Publica Mex. 2021 Nov 5;63(6, Nov-Dic):690-691. doi: 10.21149/13347. Salud Publica Mex. 2021. PMID: 35099890 Spanish.
Liposomal chemotherapeutics.
Gentile E, Cilurzo F, Di Marzio L, Carafa M, Ventura CA, Wolfram J, Paolino D, Celia C. Gentile E, et al. Future Oncol. 2013 Dec;9(12):1849-59. doi: 10.2217/fon.13.146. Future Oncol. 2013. PMID: 24295415 Review.
Southeast Asian ovalocytosis.
Martínez Vázquez C, López Rubio M, Del Orbe Barreto R. Martínez Vázquez C, et al. Med Clin (Barc). 2022 Oct 14;159(7):347-348. doi: 10.1016/j.medcli.2022.03.025. Epub 2022 Jul 21. Med Clin (Barc). 2022. PMID: 35871012 English, Spanish. No abstract available.
Celia Heyes.
Heyes C. Heyes C. Curr Biol. 2013 Feb 4;23(3):R98-100. doi: 10.1016/j.cub.2012.12.022. Curr Biol. 2013. PMID: 23520625 Free article. No abstract available.
1,698 results