Córdova-Fletes C - Search Results

1

Reduced SPAG17 Expression in Systemic Sclerosis Triggers Myofibroblast Transition and Drives Fibrosis.

Sapao P, Roberson EDO, Shi B, Assassi S, Skaug B, Lee F, Naba A, Perez White BE, Córdova-Fletes C, Tsou PS, Sawalha AH, Gudjonsson JE, Ma F, Verma P, Bhattacharyya D, Carns M, Strauss JF 3rd, Sicard D, Tschumperlin DJ, Champer MI, Campagnola PJ, Teves ME, Varga J. Sapao P, et al. Among authors: cordova fletes c. J Invest Dermatol. 2023 Feb;143(2):284-293. doi: 10.1016/j.jid.2022.08.052. Epub 2022 Sep 15. J Invest Dermatol. 2023. PMID: 36116512 Free PMC article.

2

Complete Genome Sequence of Houston Virus, a Newly Discovered Mosquito-Specific Virus Isolated from Culex quinquefasciatus in Mexico.

Cigarroa-Toledo N, Baak-Baak CM, Cetina-Trejo RC, Cordova-Fletes C, Martinez-Nuñez MA, Talavera-Aguilar LG, Garcia-Rejon JE, Torres-Chable OM, Suzan G, Blitvich BJ, Machain-Williams C. Cigarroa-Toledo N, et al. Microbiol Resour Announc. 2018 Sep 13;7(10):e00808-18. doi: 10.1128/MRA.00808-18. eCollection 2018 Sep. Microbiol Resour Announc. 2018. PMID: 30533617 Free PMC article.

3

Review of the Impact of Biofilm Formation on Recurrent Clostridioides difficile Infection.

Rubio-Mendoza D, Martínez-Meléndez A, Maldonado-Garza HJ, Córdova-Fletes C, Garza-González E. Rubio-Mendoza D, et al. Among authors: cordova fletes c. Microorganisms. 2023 Oct 10;11(10):2525. doi: 10.3390/microorganisms11102525. Microorganisms. 2023. PMID: 37894183 Free PMC article. Review.

4

Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.

Martínez-Jacobo L, Córdova-Fletes C, Ortiz-López R, Rivas F, Saucedo-Carrasco C, Rojas-Martínez A. Martínez-Jacobo L, et al. Mol Syndromol. 2013 Sep;4(6):285-91. doi: 10.1159/000353510. Mol Syndromol. 2013. PMID: 24167464 Free PMC article.

5

Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies.

Córdova-Fletes C, Becerra-Solano LE, Rangel-Sosa MM, Rivas-Estilla AM, Alberto Galán-Huerta K, Ortiz-López R, Rojas-Martínez A, Juárez-Vázquez CI, García-Ortiz JE. Córdova-Fletes C, et al. Eur J Med Genet. 2018 Mar;61(3):161-167. doi: 10.1016/j.ejmg.2017.11.011. Epub 2017 Nov 23. Eur J Med Genet. 2018. PMID: 29174089

6

A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma.

Córdova-Fletes C, Domínguez MG, Vázquez-Cárdenas A, Figuera LE, Neira VA, Rojas-Martínez A, Ortiz-López R. Córdova-Fletes C, et al. Mol Syndromol. 2012 Sep;3(3):131-135. doi: 10.1159/000341632. Epub 2012 Aug 1. Mol Syndromol. 2012. PMID: 23112755 Free PMC article.

7

De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features.

Neira VA, Romero-Espinoza P, Rojas-Martínez A, Ortiz-López R, Córdova-Fletes C, Plaja A, Barros-Núñez P. Neira VA, et al. Gene. 2013 Jul 25;524(2):381-5. doi: 10.1016/j.gene.2013.04.029. Epub 2013 Apr 29. Gene. 2013. PMID: 23639959

8

De novo dir dup/del of 18q characterized by SNP arrays and FISH in a girl child with mixed phenotypes.

Córdova-Fletes C, Sáinz-González E, Avendaño-Gálvez RI, Ramírez-Velazco A, Rivera H, Ortiz-López R, Arámbula-Meraz E, Picos-Cárdenas VJ. Córdova-Fletes C, et al. J Genet. 2014 Dec;93(3):869-73. doi: 10.1007/s12041-014-0459-8. J Genet. 2014. PMID: 25572250 Free article. No abstract available.

9

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations.

Córdova-Fletes C, Domínguez MG, Delint-Ramirez I, Martínez-Rodríguez HG, Rivas-Estilla AM, Barros-Núñez P, Ortiz-López R, Neira VA. Córdova-Fletes C, et al. Neurogenetics. 2015 Oct;16(4):287-98. doi: 10.1007/s10048-015-0452-2. Epub 2015 Jul 11. Neurogenetics. 2015. PMID: 26163108

10

A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions.

Córdova-Fletes C, Rivera H, Garza-Villarreal EA, Vázquéz-Cárdenas NA, Martínez-Jacobo LA, Moreno-Andrade T. Córdova-Fletes C, et al. Clin Dysmorphol. 2017 Jan;26(1):33-37. doi: 10.1097/MCD.0000000000000159. Clin Dysmorphol. 2017. PMID: 27750267 No abstract available.

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