J Hernandez-Yago
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Explore the profile of J Hernandez-Yago including associated specialties, affiliations and a list of published articles.
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54
Citations
250
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Recent Articles
1.
Guillen M, Corella D, Cabello M, Gonzalez J, Sabater A, Chaves J, et al.
Clin Genet
. 2005 Feb;
67(3):240-51.
PMID: 15691362
Cystinuria is an inherited metabolic disease characterized by an abnormal urinary excretion of cystine and dibasic amino acids, leading to kidney stone formation. Incidence of cystinuria in the Mediterranean Spanish...
2.
Kvetnoy I, Popuichiev V, Mikhina L, Anisimov V, Yuzhakov V, Konovalov S, et al.
Neuro Endocrinol Lett
. 2001 Oct;
22(5):337-41.
PMID: 11600875
Objectives: Diffuse neuroendocrine system (DNES) cells regulate homeostasis via neurocrine, endocrine and paracrine mechanisms. Extensive effects of peptide hormones and biogenic amines necessitate studying of DNES cell biology in aging....
3.
Gamborino M, Munoz A, Hernandez-Yago J, Renau-Piqueras J, Pinazo-Duran M
Ophthalmic Res
. 2001 Oct;
33(5):283-91.
PMID: 11586062
Thyroid hormones (TH) are essential for somatic and neural development. Epidemiological studies have pointed to TH-dependent craniofacial features occurring during development. In an attempt to elucidate the precise role of...
4.
Guillen M, Corella D, Cabello M, Saiz C, Hernandez-Yago J
Rev Clin Esp
. 2001 Jul;
201(5):256-9.
PMID: 11458794
Objective: To test the clinical usefulness of the analysis of point mutations R452W, M467T, 114C > A, 231T > A, 1136 + 3delT and 1332 + 7T > C in...
5.
Hernandez J, Blesa J, Hernandez-Yago J
Genomics
. 2000 Aug;
67(1):107-8.
PMID: 10945478
No abstract available.
6.
Blesa J, Hernandez-Yago J
Biotechniques
. 2000 May;
28(5):1019-25.
PMID: 10818710
Conformation-sensitive gel electrophoresis (CSGE) has been introduced as the most reliable method for the screening of large and multi-exon genes because of its simplicity, sensitivity and specificity. Based on heteroduplex...
7.
Guillen M, Corella D, Cabello M, Garcia A, Portoles O, Hernandez-Yago J
Hum Genet
. 2000 May;
106(3):314-20.
PMID: 10798361
Cystinuria is an inherited metabolic disease characterized by an abnormal urinary excretion of cystine and dibasic amino acids. Formation of renal calculi, recurrent infections and renal failure are the main...
8.
Guillen M, Corella D, Cabello M, Garcia A, Saiz C, Gonzalez J, et al.
Med Clin (Barc)
. 1999 Nov;
113(9):321-6.
PMID: 10562926
Background: The aim of this study has been to know the prevalence of the four most common mutations reported in SLC3A1 gene involved in human cystinuria, and to estimate the...
9.
Hernandez J, Giner P, Hernandez-Yago J
Gene
. 1999 Nov;
239(2):283-91.
PMID: 10548729
The structure of the human gene encoding the mitochondrial outer membrane receptor Tom20 has been determined from overlapping clones obtained using PCR-based techniques. The 20kb human Tom20 gene (hTom20) consists...
10.
Hernandez J, Hernandez C, Giner C, Donat V, Hernandez-Yago J
Mol Gen Genet
. 1999 Oct;
262(2):207-11.
PMID: 10517315
We report the identification and characterization of psi3Tom20, a novel processed pseudogene of the human Tom20 (hTom20) gene, which is 96.2% similarity with the hTom20 cDNA and is 5' and...