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Mostrati risultati da 1 a 12 di 12
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors 1-gen-2005 S. CorbettaL. VicentiniS. FerreroA. LaniaG. MantovaniCORDELLA, DANIELAP. Beck-PeccozA. Spada Article (author) -
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma 1-gen-2006 D. CordellaM. MuzzaP. TravagliniP. Beck-PeccozL. FugazzolaL. Persani + Article (author) -
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma 1-apr-2006 L. FugazzolaD. CordellaM. MuzzaP. Beck-PeccozL. Persani + Article (author) -
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant 1-giu-2006 L. FugazzolaD. CordellaV. CirelloM. MuzzaP. Beck PeccozL. Persani + Article (author) -
The role of Ret genotypes as modifier loci for sporadic medullary cancer 1-gen-2007 M. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. PersaniL. Fugazzola + Article (author) -
Prevalence on inactivating TSH receptor (TSHR) mutations in a large series of pediatric subjects with non-autoimmune mild hyper-thyrotropinemia (hyperTSH) 1-gen-2007 D. CordellaD. CalebiroM. BonomiP. Beck-PeccozL. Persani + Article (author) -
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer 1-mag-2007 L. FugazzolaM. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series 1-mar-2008 L. FugazzolaM. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION 1-gen-2009 R. RossettiA. MarozziD. CordellaP. Beck-PeccozL. Persani + Conference Object -
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI) 1-gen-2009 R. RossettiA. MarozziD. CordellaP. Beck-PeccozL. Persani + Conference Object -
Genetics and phenomics of hypothyroidism due to TSH resistance 1-gen-2010 L. PersaniD. CalebiroD. CordellaG. WeberG. GelminiD.V. LibriM. Bonomi + Article (author) -
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia 1-gen-2012 D. CordellaM. BonomiD.V. LibriM.C. VigoneP. Beck PeccozL. Persani + Article (author) -
Mostrati risultati da 1 a 12 di 12
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