Luca Persani researcher
Persani, Luca 1960-
Persani, Luca
VIAF ID: 311801370 (Personal)
Permalink: http://viaf.org/viaf/311801370
Preferred Forms
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100 0 _
‡a
Luca Persani
‡c
researcher
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100 1 _ ‡a Persani, Luca
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100 1 _
‡a
Persani, Luca
‡d
1960-
4xx's: Alternate Name Forms (2)
Works
| Title | Sources |
|---|---|
| An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma |
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| Induction of specific phosphodiesterase isoforms by constitutive activation of the cAMP pathway in autonomous thyroid adenomas |
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| Intracellular entrapment of wild-type TSH receptor by oligomerization with mutants linked to dominant TSH resistance. |
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| Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome: characterization of TSH carbohydrate content and bioactivity |
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| Isolated follicle-stimulating hormone (FSH) deficiency in a young man with normal virilization who did not have mutations in the FSHbeta gene |
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| JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects |
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| Lack of expression of endometrial prolactin in early implantation failure: a pilot study. |
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| Lateralization of calcitonin measurements in the wash-out fluid from thyroid fine-needle aspiration: a useful tool for the diagnosis of C-cell-hyperplasia? |
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| Lectin analyses of glycoprotein hormones in patients with congenital disorders of glycosylation |
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| Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement |
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| Loss-of-Function Variants in a Hungarian Cohort Reveal Structural Insights on TSH Receptor Maturation and Signaling |
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| Luteinizing hormone signaling in preovulatory follicles involves early activation of the epidermal growth factor receptor pathway |
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| Maturation of pituitary-thyroid function in the anencephalic fetus |
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| Measurement of cAMP accumulation in Chinese hamster ovary cells transfected with the recombinant human TSH receptor (CHO-R): a new bioassay for human thyrotropin. |
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| Mechanism of action of pituitary adenylate cyclase-activating polypeptide (PACAP) in human nonfunctioning pituitary tumors |
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| MEN1-related hyperparathyroidism: response to cinacalcet and its relationship with the calcium-sensing receptor gene variant Arg990Gly |
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| A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function |
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| Metabolic syndrome induces inflammation and impairs gonadotropin-releasing hormone neurons in the preoptic area of the hypothalamus in rabbits |
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| Modern methods to investigate the oligomerization of glycoprotein hormone receptors (TSHR, LHR, FSHR). |
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| The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studies |
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| Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome. |
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| Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect |
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| Multicenter study on TGPO autoantibody prevalence in various thyroid and non-thyroid diseases; relationships with thyroglobulin and thyroperoxidase autoantibody parameters |
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| Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes |
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| The natural history of the hyperthyrotropinemia of children born prematurely |
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| New understandings of the genetic basis of isolated idiopathic central hypogonadism. |
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| A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia. |
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| Novel NKX2-1 Frameshift Mutations in Patients with Atypical Phenotypes of the Brain-Lung-Thyroid Syndrome |
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| A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1). |
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| Off-label pasireotide treatment in one insulinoma patient with an atypical presentation and intolerant to diazoxide |
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| An open letter to the primary ovarian insufficiency community |
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| Oxytocin-induced cell growth proliferation in human myometrial cells and leiomyomas |
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| PI3K/Akt/mTOR signaling in medullary thyroid cancer: a promising molecular target for cancer therapy |
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| Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human |
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| Premature ovarian failure |
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| Prolactin and proinflammatory cytokine expression at the fetomaternal interface in first trimester miscarriage. |
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| A rare genetic disorder causing persistent severe neonatal hypoglycaemia the diagnostic workup |
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| Refining calcium test for the diagnosis of medullary thyroid cancer: cutoffs, procedures, and safety |
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| Regulation of ovulation rate in mammals: contribution of sheep genetic models |
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| Resistance to thyrotropin |
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| RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series |
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| Rituximab treatment in patients with active Graves' orbitopathy: effects on proinflammatory and humoral immune reactions. |
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| Role of GPR30 in testicular germ cell tumors: a potential new anticancer target |
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| Selective modulation of protein kinase A I and II reveals distinct roles in thyroid cell gene expression and growth. |
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| Serum levels of carboxyterminal cross-linked telopeptide of type I collagen (ICTP) in the differential diagnosis of the syndromes of inappropriate secretion of TSH |
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| Short- and long- term effects of cigarette smoke exposure on glutathione homeostasis in human bronchial epithelial cells |
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| Short-Term Exposure Effects of the Environmental Endocrine Disruptor Benzo(a)Pyrene on Thyroid Axis Function in Zebrafish |
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| Signaling by internalized G-protein-coupled receptors. |
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| Similarities and differences in the phenotype of members of an Italian family with hereditary non-autoimmune hyperthyroidism associated with an activating TSH receptor germline mutation |
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| SNPs and real-time quantitative PCR method for constitutional allelic copy number determination, the VPREB1 marker case. |
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| Somatic mutational analysis of DAX1 in testes from men with idiopathic azoospermia |
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| Sortilin is a putative postendocytic receptor of thyroglobulin |
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| SP600125 has a remarkable anticancer potential against undifferentiated thyroid cancer through selective action on ROCK and p53 pathways. |
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| Standardized Ultrasound Report for Thyroid Nodules: The Endocrinologist's Viewpoint |
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| Structural differences in the hinge region of the glycoprotein hormone receptors: evidence from the sulfated tyrosine residues |
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| Syndromes of thyroid hormone resistance. |
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| Systemic nickel allergic syndrome as an immune-mediated disease with an increased risk for thyroid autoimmunity. |
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| Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset |
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| TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature. |
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| Thyroid Cancer Stem-Like Cells: From Microenvironmental Niches to Therapeutic Strategies |
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| Thyroid gland development and function in the zebrafish model. |
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| Thyroid hemiagenesis and elevated thyrotropin levels in a child with Williams syndrome |
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| Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy. |
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| Thyrotropin Alpha- and Beta-Subunit Responses to Thyrotropin-Releasing Hormone and Domperidone in Normal Subjects and in Patients with Microprolactinomas |
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| Thyrotropin-Secreting Pituitary Adenomas |
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| Thyrotropin with decreased biological activity, a delayed consequence of cranial irradiation for nasopharyngeal carcinoma |
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| Total Iodide Organification Defect: Clinical and Molecular Characterization of an Italian Family |
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| Transplacental passage of anti-thyroid auto-antibodies in a pregnant woman with auto-immune thyroid disease |
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| TSH-induced hyperthyroidism caused by a pituitary tumor |
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| Type I interferon-mediated pathway interacts with peroxisome proliferator activated receptor-γ (PPAR-γ): at the cross-road of pancreatic cancer cell proliferation |
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| Type I interferons: ancient peptides with still under-discovered anti-cancer properties. |
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| Uncertainties in endocrine substitution therapy for central endocrine insufficiencies: hypothyroidism |
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| The unusual adequate development of a child with severe central hypothyroidsm negative at neonatal thyrotropin screening |
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| Variable carbohydrate structures of circulating thyrotropin as studied by lectin affinity chromatography in different clinical conditions |
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| Wasting syndrome with deep bradycardia as presenting manifestation of long-standing severe male hypogonadotropic hypogonadism: a case series |
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| Zebrafish as an innovative model for neuroendocrine tumors |
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