about
Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian responseCentral hypogonadotropic hypogonadism: genetic complexity of a complex diseaseAtheroprotective role of high-density lipoprotein (HDL)-associated sphingosine-1-phosphate (S1P)Distribution and function of FSH receptor genetic variants in normal menIsoforms and single nucleotide polymorphisms of the FSH receptor gene: implications for human reproductionPrevalence of olfactory and other developmental anomalies in patients with central hypogonadotropic hypogonadism.Prevalence of Y chromosome microdeletions in infertile men who consulted a tertiary care medical centre: the Münster experience.Single-nucleotide polymorphisms in the promoter region influence the expression of the human follicle-stimulating hormone receptor.Replacement of connexin43 by connexin26 in transgenic mice leads to dysfunctional reproductive organs and slowed ventricular conduction in the heart.EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.Repeated intramuscular injections of testosterone undecanoate for substitution therapy in hypogonadal men.Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.Inhibin B in male reproduction: pathophysiology and clinical relevance.Molecular diagnosis of Y chromosome microdeletions in Europe: state-of-the-art and quality control.LH and hCG action on the same receptor results in quantitatively and qualitatively different intracellular signalling.The combination of genetic variants of the FSHB and FSHR genes affects serum FSH in women of reproductive age.Krüppel-like factor 4 is involved in functional differentiation of testicular Sertoli cells.Functional genetic polymorphisms and female reproductive disorders: part II--endometriosisPhenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background.New horizons for in vitro spermatogenesis? An update on novel three-dimensional culture systems as tools for meiotic and post-meiotic differentiation of testicular germ cells.Mechanisms in endocrinology: Genetics of FSH action: a 2014-and-beyond view.Biosimilar recombinant follicle stimulating hormones in infertility treatment.Therapy of endocrine disease. Effects of chronic use of phosphodiesterase inhibitors on endothelial markers in type 2 diabetes mellitus: a meta-analysis.Chorionic gonadotropin beta-subunit gene expression in the marmoset pituitary is controlled by steroidogenic factor 1, early growth response protein 1, and pituitary homeobox factor 1.Functional and clinical consequences of mutations in the FSH receptor.In vitro bioassay for human serum follicle-stimulating hormone (FSH) based on L cells transfected with recombinant rat FSH receptor: validation of a model system.The diagnostic value of calcitonin measurement in wash-out fluid from fine-needle aspiration of thyroid nodules in the diagnosis of medullary thyroid cancer.A search for circulating immunoglobulins blocking follicle-stimulating hormone action in male idiopathic infertility.An activated human follicle-stimulating hormone (FSH) receptor stimulates FSH-like activity in gonadotropin-deficient transgenic mice.cynDAZLA: a cynomolgus monkey homologue of the human autosomal DAZ gene.Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism.Follicle-stimulating-hormone receptor and twinning.Is inhibin B a pharmacodynamic parameter for FSH in normal men?Age-related changes in plasma dehydroepiandrosterone sulphate, cortisol, testosterone and free testosterone circadian rhythms in adult men.Reassembly of somatic cells and testicular organogenesis in vitro.Self-adjusted postmenopausal hormone replacement therapy: effects on the biological and immunological profile of FSH and correlation to climacteric symptoms.Maintenance of spermatogenesis in hypogonadotropic hypogonadal men with human chorionic gonadotropin alone.A common haplotype of protamine 1 and 2 genes is associated with higher sperm counts.The prognostic value of miRNA146a in follicular thyroid carcinoma.KRP-203, sphingosine 1-phosphate receptor type 1 agonist, ameliorates atherosclerosis in LDL-R-/- mice.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Manuela Simoni
@ast
Manuela Simoni
@en
Manuela Simoni
@es
Manuela Simoni
@nl
Manuela Simoni
@sl
type
label
Manuela Simoni
@ast
Manuela Simoni
@en
Manuela Simoni
@es
Manuela Simoni
@nl
Manuela Simoni
@sl
prefLabel
Manuela Simoni
@ast
Manuela Simoni
@en
Manuela Simoni
@es
Manuela Simoni
@nl
Manuela Simoni
@sl
P1053
A-9600-2013
P106
P1153
7005805305
P21
P2798
P31
P3829
P496
0000-0002-2133-4304