Juan C. Zenteno - Search Results

Year	Number of Results
2002	4
2003	1
2004	5
2005	5
2006	4
2007	3
2008	6
2009	6
2010	6
2011	5
2012	8
2013	17
2014	14
2015	13
2016	11
2017	15
2018	10
2019	12
2020	8
2021	1
2022	12
2023	12
2024	7

1

Genes relacionados con microftalmia y anoftalmia hereditarias.

Matías-Pérez D, García-Montalvo IA, Zenteno JC. Matías-Pérez D, et al. Gac Med Mex. 2017;153(7):824-829. doi: 10.24875/GMM.17002604. Gac Med Mex. 2017. PMID: 29414965 Free article. Review.

2

Familial Hypercholesterolemia: Update and Review.

Chacón-Camacho OF, Pozo-Molina G, Méndez-Catalá CF, Reyes-Reali J, Méndez-Cruz R, Zenteno JC. Chacón-Camacho OF, et al. Endocr Metab Immune Disord Drug Targets. 2022;22(2):198-211. doi: 10.2174/1871530321666210208212148. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 33563162

3

Single cell RNA sequencing confirms retinal microglia activation associated with early onset retinal degeneration.

Kumari A, Ayala-Ramirez R, Zenteno JC, Huffman K, Sasik R, Ayyagari R, Borooah S. Kumari A, et al. Sci Rep. 2022 Sep 10;12(1):15273. doi: 10.1038/s41598-022-19351-w. Sci Rep. 2022. PMID: 36088481 Free PMC article.

4

Genetic Aspects of Glaucoma: An Updated Review.

Chacon-Camacho OF, Arce-Gonzalez R, Sanchez-de la Rosa F, Urióstegui-Rojas A, Hofmann-Blancas EM, Mata-Flores F, Zenteno JC. Chacon-Camacho OF, et al. Curr Mol Med. 2023 Jun 2. doi: 10.2174/1566524023666230602143617. Online ahead of print. Curr Mol Med. 2023. PMID: 37272463

5

The clinical implications of molecular monitoring and analyses of inherited retinal diseases.

Chacón-Camacho OF, García-Montaño LA, Zenteno JC. Chacón-Camacho OF, et al. Among authors: zenteno jc. Expert Rev Mol Diagn. 2017 Nov;17(11):1009-1021. doi: 10.1080/14737159.2017.1384314. Epub 2017 Oct 5. Expert Rev Mol Diagn. 2017. PMID: 28945154 Review.

6

USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients.

Ordoñez-Labastida V, Chacon-Camacho OF, Lopez-Rodriguez VR, Zenteno JC. Ordoñez-Labastida V, et al. Among authors: zenteno jc. Mol Vis. 2023 Apr 29;29:31-38. eCollection 2023. Mol Vis. 2023. PMID: 37287646 Free PMC article.

7

[Gene therapy for hereditary ophthalmological diseases: Advances and future perspectives].

Chacón-Camacho ÓF, Astorga-Carballo A, Zenteno JC. Chacón-Camacho ÓF, et al. Gac Med Mex. 2015 Jul-Aug;151(4):501-11. Gac Med Mex. 2015. PMID: 26290027 Free article. Review. Spanish.

8

Review and update on the molecular basis of Leber congenital amaurosis.

Chacon-Camacho OF, Zenteno JC. Chacon-Camacho OF, et al. World J Clin Cases. 2015 Feb 16;3(2):112-24. doi: 10.12998/wjcc.v3.i2.112. World J Clin Cases. 2015. PMID: 25685757 Free PMC article. Review.

9

SOX2 anophthalmia syndrome and dental anomalies.

Chacon-Camacho OF, Fuerte-Flores BI, Ricardez-Marcial EF, Zenteno JC. Chacon-Camacho OF, et al. Am J Med Genet A. 2015 Nov;167A(11):2830-3. doi: 10.1002/ajmg.a.37277. Epub 2015 Aug 6. Am J Med Genet A. 2015. PMID: 26250054

10

MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.

Corona-Rivera JR, Zenteno JC, Ordoñez-Labastida V, Cruz-Cruz JP, Cortés-Pastrana RC, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Martínez-Herrera A. Corona-Rivera JR, et al. Eur J Med Genet. 2023 Oct;66(10):104826. doi: 10.1016/j.ejmg.2023.104826. Epub 2023 Aug 30. Eur J Med Genet. 2023. PMID: 37657631

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