BIOQUÍMICA Y BIOLOGÍA MOLECULAR I
Departamento
Hospital Universitari de Bellvitge
l'Hospitalet de Llobregat, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitari de Bellvitge (10)
2022
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Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome
Journal of Personalized Medicine, Vol. 12, Núm. 6
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Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility
Andrology, Vol. 10, Núm. 7, pp. 1339-1350
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Communications Biology, Vol. 5, Núm. 1
2021
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Common gene variants within 3′-untranslated regions as modulators of multiple myeloma risk and survival
International Journal of Cancer, Vol. 148, Núm. 8, pp. 1887-1894
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Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
Andrology, Vol. 9, Núm. 4, pp. 1151-1165
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SMARCA4 deficient tumours are vulnerable to KDM6A/UTX and KDM6B/JMJD3 blockade
Nature Communications, Vol. 12, Núm. 1
2020
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Comprehensive analysis of SWI/SNF inactivation in lung adenocarcinoma cell models
Cancers, Vol. 12, Núm. 12, pp. 1-14
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Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment
Fertility and Sterility, Vol. 114, Núm. 2, pp. 398-406
2010
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Gene amplification of the transcription factor DP1 and CTNND1 in human lung cancer
Journal of Pathology, Vol. 222, Núm. 1, pp. 89-98