Campos Y - Search Results

1

Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I.

Mosca R, van de Vlekkert D, Campos Y, Fremuth LE, Cadaoas J, Koppaka V, Kakkis E, Tifft C, Toro C, Allievi S, Gellera C, Canafoglia L, Visser G, Annunziata I, d'Azzo A. Mosca R, et al. Among authors: campos y. J Clin Med. 2020 Mar 4;9(3):695. doi: 10.3390/jcm9030695. J Clin Med. 2020. PMID: 32143456 Free PMC article.

2

New mutations in two Dutch patients with early infantile galactosialidosis.

Groener J, Maaswinkel-Mooy P, Smit V, van der Hoeven M, Bakker J, Campos Y, d'Azzo A. Groener J, et al. Among authors: campos y. Mol Genet Metab. 2003 Mar;78(3):222-8. doi: 10.1016/s1096-7192(03)00005-2. Mol Genet Metab. 2003. PMID: 12649068

3

Ozz-E3, a muscle-specific ubiquitin ligase, regulates beta-catenin degradation during myogenesis.

Nastasi T, Bongiovanni A, Campos Y, Mann L, Toy JN, Bostrom J, Rottier R, Hahn C, Conaway JW, Harris AJ, D'Azzo A. Nastasi T, et al. Among authors: campos y. Dev Cell. 2004 Feb;6(2):269-82. doi: 10.1016/s1534-5807(04)00020-6. Dev Cell. 2004. PMID: 14960280 Free article.

4

Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase.

Loren DJ, Campos Y, d'Azzo A, Wyble L, Grange DK, Gilbert-Barness E, White FV, Hamvas A. Loren DJ, et al. Among authors: campos y. J Perinatol. 2005 Jul;25(7):491-4. doi: 10.1038/sj.jp.7211335. J Perinatol. 2005. PMID: 15908988

5

Heterodimerization of the sialidase NEU1 with the chaperone protective protein/cathepsin A prevents its premature oligomerization.

Bonten EJ, Campos Y, Zaitsev V, Nourse A, Waddell B, Lewis W, Taylor G, d'Azzo A. Bonten EJ, et al. Among authors: campos y. J Biol Chem. 2009 Oct 9;284(41):28430-28441. doi: 10.1074/jbc.M109.031419. Epub 2009 Aug 7. J Biol Chem. 2009. PMID: 19666471 Free PMC article.

6

Ozz-E3 ubiquitin ligase targets sarcomeric embryonic myosin heavy chain during muscle development.

Campos Y, Qiu X, Zanoteli E, Moshiach S, Vergani N, Bongiovanni A, Harris AJ, d'Azzo A. Campos Y, et al. PLoS One. 2010 Mar 24;5(3):e9866. doi: 10.1371/journal.pone.0009866. PLoS One. 2010. PMID: 20352047 Free PMC article.

7

Regulated lysosomal exocytosis mediates cancer progression.

Machado E, White-Gilbertson S, van de Vlekkert D, Janke L, Moshiach S, Campos Y, Finkelstein D, Gomero E, Mosca R, Qiu X, Morton CL, Annunziata I, d'Azzo A. Machado E, et al. Among authors: campos y. Sci Adv. 2015 Dec 18;1(11):e1500603. doi: 10.1126/sciadv.1500603. eCollection 2015 Dec. Sci Adv. 2015. PMID: 26824057 Free PMC article.

8

Excessive exosome release is the pathogenic pathway linking a lysosomal deficiency to generalized fibrosis.

van de Vlekkert D, Demmers J, Nguyen XX, Campos Y, Machado E, Annunziata I, Hu H, Gomero E, Qiu X, Bongiovanni A, Feghali-Bostwick CA, d'Azzo A. van de Vlekkert D, et al. Among authors: campos y. Sci Adv. 2019 Jul 17;5(7):eaav3270. doi: 10.1126/sciadv.aav3270. eCollection 2019 Jul. Sci Adv. 2019. PMID: 31328155 Free PMC article.

9

MYC competes with MiT/TFE in regulating lysosomal biogenesis and autophagy through an epigenetic rheostat.

Annunziata I, van de Vlekkert D, Wolf E, Finkelstein D, Neale G, Machado E, Mosca R, Campos Y, Tillman H, Roussel MF, Andrew Weesner J, Ellen Fremuth L, Qiu X, Han MJ, Grosveld GC, d'Azzo A. Annunziata I, et al. Among authors: campos y. Nat Commun. 2019 Aug 9;10(1):3623. doi: 10.1038/s41467-019-11568-0. Nat Commun. 2019. PMID: 31399583 Free PMC article.

10

Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations.

Han MJ, Annunziata I, Weesner J, Campos Y, Salie M, O'Reilly C, d'Azzo A. Han MJ, et al. Among authors: campos y. Stem Cell Res. 2020 Jul;46:101836. doi: 10.1016/j.scr.2020.101836. Epub 2020 May 6. Stem Cell Res. 2020. PMID: 32485644 Free PMC article.

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