Zobrazeno 1 - 10
of 24
pro vyhledávání: '"J. L. San Millán"'
Autor:
Manuel Luque-Ramírez, José I. Botella-Carretero, Francisco Álvarez-Blasco, Héctor F. Escobar-Morreale, Gemma Villuendas, J. L. San Millán, Raul Sanchón
Publikováno v:
Human Reproduction. 21:2257-2265
Background We conducted a cross-sectional case-control study to evaluate the possible involvement of adiponectin and resistin in the pathogenesis of polycystic ovary syndrome (PCOS). Methods Seventy-six PCOS patients and 40 non-hyperandrogenic women
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55db37f7ee4cf51f88498b41eda53707
https://doi.org/10.1093/humrep/del146
https://doi.org/10.1093/humrep/del146
Autor:
Gemma Villuendas, José I. Botella-Carretero, J. L. San Millán, Héctor F. Escobar-Morreale, J. Sancho
Publikováno v:
Scopus-Elsevier
Increased serum inflammatory markers have been found in obesity and insulin-resistant states, and could play a causative role in insulin resistance, atherosclerosis and cardiovascular disease. The polycystic ovary syndrome represents a human model of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2be8ab7bc5fb7fcb40e1800d3805f51
https://doi.org/10.1007/s00125-003-1090-z
https://doi.org/10.1007/s00125-003-1090-z
Autor:
David Reynolds, Peter C. Harris, Xosé M. Lens, Toshio Mochizuki, D Telleria, R. Alonso, Stefan Somlo, F Moreno, M Viribay, J L San Millán, Tomohito Hayashi
Publikováno v:
Human Genetics. 101:229-234
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most frequent inherited disorders. The majority of cases are due to mutation of the PKD1 gene, on 16p13.3, while in most of the remainder the disease maps to the PKD2 locus, at chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75308074cc54622cb9b625f05f3a54a
https://doi.org/10.1007/s004390050621
https://doi.org/10.1007/s004390050621
Autor:
Mariana Herrera, Alberto R. Kornblihtt, J L San Millán, Viviana Bernath, Diana M. Iglesias, M Viribay, Rubén Martín, Elvira Arrizurieta, A Fraga, M Virginillo
Publikováno v:
Journal of Medical Genetics. 34:827-830
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder with genetic heterogeneity. Up to three loci are involved in this disease, PKD1 on chromosome 16p13.3, PKD2 on 4q21, and a third locus of unknown location. Here we report t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e818119dc86b655efd7e647fc3dc3f
https://doi.org/10.1136/jmg.34.10.827
https://doi.org/10.1136/jmg.34.10.827
Publikováno v:
The Journal of Experimental Medicine
In murine T cell development, early thymocytes that productively rearrange the T cell receptor (TCR) beta locus are selected to continue maturation, before TCR alpha expression, by means of a pre-TCR alpha- (pT alpha-) TCR beta heterodimer (pre-TCR).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4ef9082f55ebc3b9339f24ce0d66e4e
http://europepmc.org/articles/PMC2192728
http://europepmc.org/articles/PMC2192728
Publikováno v:
Journal of Bacteriology. 177:7131-7140
The translation inhibitor microcin C7 (MccC7) is a linear heptapeptide whose N terminus has been replaced by an N-formyl group and whose C terminus has been replaced by the phosphodiester of 5'-adenylic acid and n-aminopropanol (J. I. Guijarro, J. E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3286af368b6b34a591703ccc1ac8ccae
https://doi.org/10.1128/jb.177.24.7131-7140.1995
https://doi.org/10.1128/jb.177.24.7131-7140.1995
Autor:
M, Marco-Mingot, J L, San-Millán, W, Wuyts, J, Bachiller-Corral, W, Van Hul, A A, Morales-Piga
Publikováno v:
Clinical genetics. 60(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09c1cfbffdb45021b2af3cbd54ca2225
https://pubmed.ncbi.nlm.nih.gov/11531977
https://pubmed.ncbi.nlm.nih.gov/11531977
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(7)
We prospectively estimated the prevalence of the polycystic ovary syndrome (PCOS), as defined by the NIH/NICHHD 1990 endocrine criteria, in a population of 154 Caucasian women of reproductive age reporting spontaneously for blood donation. Anthropome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b579b19781bb079c4f7ba25ae0548afb
https://pubmed.ncbi.nlm.nih.gov/10902790
https://pubmed.ncbi.nlm.nih.gov/10902790
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(4)
The human androgen receptor (AR) gene contains a variable number of CAG repeats within exon 1. Shorter AR alleles, by increasing transactivation, may result in augmented AR-mediated sensitivity of the hair follicle. We have evaluated whether the numb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee4448aa80b5adfe0d8377c7b2c483d7
https://pubmed.ncbi.nlm.nih.gov/10770223
https://pubmed.ncbi.nlm.nih.gov/10770223
Dinucleotide repeat polymorphism at the D4S2458 locus close to the PKD2 locus on human chromosome 4q
Publikováno v:
Human genetics. 95(5)
A new polymorphic CA repeat sequence was identified within the candidate region for the autosomal dominant polycystic kidney disease-type 2 (PKD2) locus. It should be a useful marker in the localization of this gene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b1f85dbc81a5f0b9670597c21e8649a
https://pubmed.ncbi.nlm.nih.gov/7759091
https://pubmed.ncbi.nlm.nih.gov/7759091