[Concentration of androgen-binding proteins in the rat gonad treated with estrogens and testosterone]

Induction of hormone-sensitive lipase/cholesteryl esterase gene expression by C/EBPα independently of the PKA pathway in the adrenocortical Y-1 cells.

Steroids·2015

SF-1 (NR5A1) expression is stimulated by the PKA pathway and is essential for the PKA-induced activation of LIPE expression in Y-1 cells.

Molecular and cellular biochemistry·2015

A novel insA2933 causes premature termination of translation and is accompanied by overexpression of truncated androgen receptor gene in a patient with complete androgen insensitivity syndrome.

Journal of applied genetics·2015

Identification of mutations in the HVR1 and PKR-BD regions in HCV-infected patients resistant to PEG-IFNα/RBV therapy.

Journal of applied genetics·2015

Application of a high-resolution melting technique for the rapid detection of partial replacement of HCV-1b by HCV-1a after PEG-IFNα/RBV therapy.

Journal of applied genetics·2014

A rare heterozygous TRAF6 variant is associated with hypohidrotic ectodermal dysplasia.

The British journal of dermatology·2012

The association between abdominal muscle mass quantified by computed tomography and osteoporosis in postmenopausal women.

Endokrynologia Polska·2026

Beyond traditional biopsy: integrating liquid biopsy, molecular panels, and advanced imaging techniques in thyroid cancer management.

Endokrynologia Polska·2026

Estimating obesity phenotype features in a real-world cohort - a non-interventional pilot study using an original questionnaire.

Endokrynologia Polska·2026

Type 5 diabetes mellitus: revisiting malnutrition-related diabetes.

Endokrynologia Polska·2026

Hypophosphatemic rickets in children: current knowledge and a proposal for a diagnostic algorithm.

Endokrynologia Polska·2026

Association between Helicobacter pylori infection and hyperandrogenism in women with polycystic ovary syndrome.

Endokrynologia Polska·2026

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Mutation research. Reviews in mutation research·2026

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

AJP reports·2026

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Mitochondrial DNA. Part B, Resources·2026

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cytogenetic and genome research·2026

Related Experiment Videos

[Concentration of androgen-binding proteins in the rat gonad treated with estrogens and testosterone]

Related Concept Videos

Induction of hormone-sensitive lipase/cholesteryl esterase gene expression by C/EBPα independently of the PKA pathway in the adrenocortical Y-1 cells.

SF-1 (NR5A1) expression is stimulated by the PKA pathway and is essential for the PKA-induced activation of LIPE expression in Y-1 cells.

A novel insA2933 causes premature termination of translation and is accompanied by overexpression of truncated androgen receptor gene in a patient with complete androgen insensitivity syndrome.

Identification of mutations in the HVR1 and PKR-BD regions in HCV-infected patients resistant to PEG-IFNα/RBV therapy.

Application of a high-resolution melting technique for the rapid detection of partial replacement of HCV-1b by HCV-1a after PEG-IFNα/RBV therapy.

A rare heterozygous TRAF6 variant is associated with hypohidrotic ectodermal dysplasia.

The association between abdominal muscle mass quantified by computed tomography and osteoporosis in postmenopausal women.

Beyond traditional biopsy: integrating liquid biopsy, molecular panels, and advanced imaging techniques in thyroid cancer management.

Estimating obesity phenotype features in a real-world cohort - a non-interventional pilot study using an original questionnaire.

Type 5 diabetes mellitus: revisiting malnutrition-related diabetes.

Hypophosphatemic rickets in children: current knowledge and a proposal for a diagnostic algorithm.

Association between Helicobacter pylori infection and hyperandrogenism in women with polycystic ovary syndrome.

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Related Experiment Videos

[Concentration of androgen-binding proteins in the rat gonad treated with estrogens and testosterone]

Related Concept Videos

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