Zobrazeno 1 - 10
of 768
pro vyhledávání: '"L. Becherini"'
Autor:
Qadir, Ayyaz1 (AUTHOR), Singh, Nabita1 (AUTHOR), Dean, Jenna2 (AUTHOR), Brown, Kerryn2 (AUTHOR), Tacey, Mark2 (AUTHOR), Mann, Bruce3,4 (AUTHOR), Kron, Tomas4,5 (AUTHOR), Cahoon, Glenn2 (AUTHOR), Lau, Eddie4,6,7 (AUTHOR), Scott, Andrew M.7,8 (AUTHOR), Yeo, Belinda8,9 (AUTHOR), Loh, Su-Wen10 (AUTHOR), Uribe, Sergio1 (AUTHOR), Moe, Aung Aung Kywe1 (AUTHOR), Ireland-Jenkins, Kerryn4,11 (AUTHOR), McAuley, Rosly2 (AUTHOR), McDermont, Leah2 (AUTHOR), Ooi, Wei Ming10 (AUTHOR), Ng, Suat10 (AUTHOR), Chao, Michael1,2 (AUTHOR)
Publikováno v:
Pilot & Feasibility Studies. 11/7/2024, Vol. 10 Issue 1, p1-9. 9p.
Autor:
Klyucherev, Timofey O.1,2 (AUTHOR), Peshkova, Maria A.1 (AUTHOR), Revokatova, Daria P.1,2 (AUTHOR), Serejnikova, Natalia B.1,3 (AUTHOR), Fayzullina, Nafisa M.1 (AUTHOR), Fayzullin, Alexey L.1,3 (AUTHOR), Ershov, Boris P.1 (AUTHOR), Khristidis, Yana I.1 (AUTHOR), Vlasova, Irina I.1 (AUTHOR), Kosheleva, Nastasia V.1,2 (AUTHOR), Svistunov, Andrey A.4 (AUTHOR), Timashev, Peter S.1,2,5 (AUTHOR) timashev_p_s@staff.sechenov.ru
Publikováno v:
International Journal of Molecular Sciences. Nov2024, Vol. 25 Issue 21, p11564. 22p.
Autor:
Mario Serio, Massimo Mannelli, Michaela Luconi, L. Becherini, Elisabetta Piscitelli, Adriana Lombardi, Tonino Ercolino, M. S. Gaglianò, Giulia Cantini
Publikováno v:
Clinical Endocrinology. 69:253-258
Summary Context Medullary thyroid carcinoma (MTC) is the most common feature of multiple endocrine neoplasia type 2A (MEN2A) and occurs in almost all patients affected by germline RET mutations. Objective We identified and characterized an activating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5421df281419987ca6680f89b5ab1a83
https://doi.org/10.1111/j.1365-2265.2008.03197.x
https://doi.org/10.1111/j.1365-2265.2008.03197.x
Autor:
Matteo Ramazzotti, Nico Console, Maria Sole Gaglianò, Donatella Degl'Innocenti, Andrea Valeri, Elisa Piscitelli, Pamela Pinzani, Gabriella Nesi, Michele Maiello, Tonino Ercolino, Carlo Bergamini, Gabriele Parenti, L. Becherini, Lisa Simi, Massimo Mannelli
Publikováno v:
Clinical Endocrinology. 68:762-768
Summary Context The von Hippel-Lindau (VHL) syndrome is an inherited multitumour disorder characterized by clinical heterogeneity and high penetrance. Pheochromocytoma (Pheo) is present in 10%–15% of cases and can be isolated or associated with oth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4297b8b33c203586bd29545e198b9fdc
https://doi.org/10.1111/j.1365-2265.2007.03131.x
https://doi.org/10.1111/j.1365-2265.2007.03131.x
Autor:
Massimo Mannelli, Gabriele Parenti, M. S. Gaglianò, Lisa Simi, L. Becherini, Tonino Ercolino, Giuseppe Opocher
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 115:160-165
The familial forms of pheochromocytoma have recently been demonstrated to be more frequent than believed in the past. The genes currently known to be responsible for tumor formation are RET, VHL, NF1, SDHB, SDHC and SDHD. Germline mutations of these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9546fa20d03aeaf26a7a960b63e1f285
https://doi.org/10.1055/s-2007-970407
https://doi.org/10.1055/s-2007-970407
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 81:1-24
Osteoporosis is a common skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility and susceptibility to fracture. In the past years, twin and family study have sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76de44692409cdd3952767fc3fd75249
https://doi.org/10.1016/s0960-0760(02)00043-2
https://doi.org/10.1016/s0960-0760(02)00043-2
Autor:
Emanuela Colli, Alberto Falchetti, Antonietta Amedei, Maria Luisa Brandi, Maria Farci, Sandra Silvestri, L. Becherini, Luigi Gennari, Stefano Gonnelli, Laura Masi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:2263-2269
Conversion of C19 steroids to estrogens is catalyzed by the aromatase enzyme. Inactivating mutations of the aromatase gene are associated with decreased bone mineral density in both men and women. Genetic studies suggest that several genes contribute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17f8d4fb106faa0aceaef7442e25b0e9
https://doi.org/10.1210/jcem.86.5.7450
https://doi.org/10.1210/jcem.86.5.7450
Autor:
Annamaria Morelli, Gianna Fiorelli, Stefano Gonnelli, Francesco Massart, Laura Masi, Maria Luisa Brandi, R Mansani, Alberto Falchetti, Annalisa Tanini, L. Becherini, Luigi Gennari
Publikováno v:
Human Molecular Genetics. 9:2043-2050
Bone mineral density (BMD), the major determinant of osteoporotic fracture risk, has a strong genetic component. The discovery that inactivation of estrogen receptor alpha (ERalpha) gene is associated with low BMD indicated ERalpha as a candidate gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eca2c90f837ea4978ed04e83930bf849
https://doi.org/10.1093/hmg/9.13.2043
https://doi.org/10.1093/hmg/9.13.2043
Autor:
Alberto Falchetti, Valentina Martineti, Eitan Friedman, M. Mark, M. L. Brandi, L. Becherini, Annamaria Morelli
Publikováno v:
European Journal of Endocrinology. :131-137
Multiple endocrine neoplasia type 1 (MEN 1) is a familial syndrome characterized by parathyroid, enteropancreatic and pituitary tumors. The gene responsible for this syndrome is localized at chromosomal 11q13 region and DNA markers from this region c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::583f56af922cafee3981ff2f087ce279
https://doi.org/10.1530/eje.0.1420131
https://doi.org/10.1530/eje.0.1420131
Autor:
Susanna Benvenuti, Valentina Martineti, L. Becherini, Lucia Picariello, Annamaria Morelli, Alberto Falchetti, Luigi Gennari, Cesare Bordi, Maria Luisa Brandi, Rinaldo Lampugnani
Publikováno v:
Biochemical and Biophysical Research Communications. 265:252-255
Telomerase results to be active in human germ, stem cells, several malignant cell tumors and in immortalized cell lines. In order to investigate if molecular mechanisms other than Rb gene inactivation can be helpful to diagnose malignancy of parathyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87333c55cc633a7f3a5b742e5baef3d5
https://doi.org/10.1006/bbrc.1999.1320
https://doi.org/10.1006/bbrc.1999.1320