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M Mannelli

Showing results (101-110 of 434) with videos related to

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International Journal of Andrology|April 1, 1981
Spermatic and peripheral oestradiol levels in patients affected by azoospermia due to seminiferous tubular damageG Forti, G Giusti, M Pazzagli, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Variable expression of the transcription factors cAMP response element-binding protein and inducible cAMP early repressor in the normal adrenal cortex and in adrenocortical adenomas and carcinomasA Peri, P Luciani, B Conforti, et al.
Endocrine-Related Cancer|December 23, 2004
Distinct gene expression profiles in norepinephrine- and epinephrine-producing hereditary and sporadic pheochromocytomas: activation of hypoxia-driven angiogenic pathways in von Hippel-Lindau syndromeG Eisenhofer, T-T Huynh, K Pacak, et al.
Journal of Medical Genetics|August 3, 2005
Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109XL Simi, R Sestini, P Ferruzzi, et al.
Cancer Letters|October 19, 2020
The cytoskeleton actin binding protein filamin A impairs both IGF2 mitogenic effects and the efficacy of IGF1R inhibitors in adrenocortical cancer cellsR Catalano, E Giardino, D Treppiedi, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypesG Eisenhofer, M M Walther, T T Huynh, et al.
Journal of Endocrinological Investigation|March 12, 2020
A unique neuroendocrine cell model derived from the human foetal neural crestE Rapizzi, S Benvenuti, C Deledda, et al.
Journal of Endocrinological Investigation|January 16, 2023
Carbonic anhydrases III and IX are new players in the crosstalk between adrenocortical carcinoma and its altered adipose microenvironmentL Fei, G Cantini, A Nocentini, et al.
Annals of the New York Academy of Sciences|November 15, 2006
SDH mutations in patients affected by paraganglioma syndromes: a personal experienceM Mannelli, L Simi, T Ercolino, et al.
European Journal of Endocrinology|April 29, 2015
Immunohistochemical expression of stem cell markers in pheochromocytomas/paragangliomas is associated with SDHx mutationsL Oudijk, C M Neuhofer, U D Lichtenauer, et al.
Pageof 44

Showing results (101-110 of 434) with videos related to

Sort By:
Pageof 44
International Journal of Andrology|April 1, 1981
Spermatic and peripheral oestradiol levels in patients affected by azoospermia due to seminiferous tubular damageG Forti, G Giusti, M Pazzagli, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Variable expression of the transcription factors cAMP response element-binding protein and inducible cAMP early repressor in the normal adrenal cortex and in adrenocortical adenomas and carcinomasA Peri, P Luciani, B Conforti, et al.
Endocrine-Related Cancer|December 23, 2004
Distinct gene expression profiles in norepinephrine- and epinephrine-producing hereditary and sporadic pheochromocytomas: activation of hypoxia-driven angiogenic pathways in von Hippel-Lindau syndromeG Eisenhofer, T-T Huynh, K Pacak, et al.
Journal of Medical Genetics|August 3, 2005
Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109XL Simi, R Sestini, P Ferruzzi, et al.
Cancer Letters|October 19, 2020
The cytoskeleton actin binding protein filamin A impairs both IGF2 mitogenic effects and the efficacy of IGF1R inhibitors in adrenocortical cancer cellsR Catalano, E Giardino, D Treppiedi, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypesG Eisenhofer, M M Walther, T T Huynh, et al.
Journal of Endocrinological Investigation|March 12, 2020
A unique neuroendocrine cell model derived from the human foetal neural crestE Rapizzi, S Benvenuti, C Deledda, et al.
Journal of Endocrinological Investigation|January 16, 2023
Carbonic anhydrases III and IX are new players in the crosstalk between adrenocortical carcinoma and its altered adipose microenvironmentL Fei, G Cantini, A Nocentini, et al.
Annals of the New York Academy of Sciences|November 15, 2006
SDH mutations in patients affected by paraganglioma syndromes: a personal experienceM Mannelli, L Simi, T Ercolino, et al.
European Journal of Endocrinology|April 29, 2015
Immunohistochemical expression of stem cell markers in pheochromocytomas/paragangliomas is associated with SDHx mutationsL Oudijk, C M Neuhofer, U D Lichtenauer, et al.
Pageof 44