Zobrazeno 1 - 10
of 52
pro vyhledávání: '"R. Gruppioni"'
Autor:
L Lenzi, R. Gruppioni, Nicoletta Zini, A. Sensi, Laura Roncuzzi, Dino Amadori, L. Ricotti, Wainer Zoli, Anna Gasperi-Campani
Publikováno v:
Cancer Genetics and Cytogenetics. 107:11-20
Two human cancer cell lines were established from metastatic lesions of an adenocarcinoma (RAL) and a squamous cell (CAEP) carcinoma of the lung. The clinical histories of the patients from whom the cell lines were derived are reported. The lines wer
Autor:
R. Gruppioni, A. Sensi, Anna Gasperi-Campani, L. Ricotti, Laura Roncuzzi, Nicoletta Zini, Dino Amadori, Wainer Zoli, L Lenzi
Publikováno v:
Cancer Genetics and Cytogenetics. 105:43-49
A new cancer cell line (KKP) was established from an ascitic effusion of an advanced gastric adenocarcinoma, intestinal type. The line has been maintained in continuous monolayer culture with a doubling time of 48 hours for more than 2 years. KKP cel
Autor:
Fulvia Farabegoli, A. Sensi, Wainer Zoli, Laura Roncuzzi, Dino Amadori, Anna Gasperi-Campani, Nicoletta Zini, R. Gruppioni, L Lenzi
Publikováno v:
European Journal of Cancer. 34:724-730
A new human cancer cell line was established from a metastatic lesion of a small cell lung carcinoma (SCLC-R1) and maintained in continuous culture with a doubling time of 62 h. The SCLC-R1 line, whose ultrastructural features are presented, showed a
Autor:
L Lenzi, Wainer Zoli, A. Sensi, Anna Gasperi-Campani, Laura Roncuzzi, F. Barzanti, Nicoletta Zini, R. Gruppioni, Dino Amadori
Publikováno v:
Breast Cancer Research and Treatment. 43:141-151
Two human cancer cell lines (MA 2 and MA 3) were established from pleural effusions of infiltrating ductal carcinomas of the breast. The lines were maintained in continuous monolayer culture with doubling times of 70 (MA 2) and 78 (MA 3) hr for more
Autor:
A. Sensi, A Flamigni, Laura Roncuzzi, Wainer Zoli, R. Gruppioni, Nicoletta Zini, Anna Gasperi-Campani, Dino Amadori
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 122:237-242
We established a novel cancer cell line (MAST) from the ascitic fluid of a metastatic infiltrating ductal carcinoma of the breast. The epithelial and neoplastic nature of the MAST cells was confirmed by ultrastructural analysis. The cell line was mai
Autor:
P, Prontera, B, Buldrini, V, Aiello, D, Rogaia, A, Mencarelli, R, Gruppioni, A, Bonfatti, N, Beltrami, E, Donti, A, Sensi
Publikováno v:
Genetic counseling (Geneva, Switzerland). 21(1)
A pericentric inversion of chromosome 18 [inv(18)(p11.32q22)] and its recombinants has been studied in a three-generation family. A mother/son couple, carrying the rec dup(18q), showed dysmorphisms and short stature but only the son had mild mental r
Autor:
R. Gruppioni, G. Sbrenna
Publikováno v:
Ethology Ecology & Evolution. 4:105-109
Total proteins from different Kalotermes flavicollis castes were electrophoretically analyzed. Results reveal the presence of different proteins in terminal castes and in developmental stages. The ...
Autor:
V, Aiello, N, Astolfi, R, Gruppioni, B, Buldrini, P, Prontera, A, Bonfatti, A, Sensi, E, Calzolari
Publikováno v:
Genetic counseling (Geneva, Switzerland). 18(4)
We report on the second prenatal diagnosis of familial paracentric inversion of the long arm of Y chromosome [46, X, inv(Y)(q11.2q12)]. The anomaly was detected through an amniocentesis performed because of advanced maternal age. The inversion has be
Autor:
Barbara Buldrini, Paolo Prontera, A. Sensi, R. Gruppioni, Elisa Calzolari, V. Aiello, Silvia Palma, Stefano Volinia, Alessandro Martini
Publikováno v:
American journal of medical genetics. Part A. (1)
We report on a 3-year-old child who presented a de novo rearrangement of chromosome 4, detected on GTG banding and characterized by array CGH and FISH, as a complex intrachromosomal rearrangement with three deletions: del(q32.1q32.2), del(q33q34.1),
Autor:
A. Bonfatti, Alessandra Ferlini, Venti G, V. Aiello, Elisa Calzolari, Barbara Buldrini, R. Gruppioni, A. Sensi, Paolo Prontera, Emilio Donti
We describe a 4-year-old female child with severe global mental retardation, myoclonic epilepsy, proximal hypotonia and dysmorphisms, whose prenatal diagnosis following amniocentesis revealed a constitutional female karyotype carrying a t(1;15)(q10;p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df4ba87f2d9e88fb1dfe933bd786b21
http://hdl.handle.net/11391/151455
http://hdl.handle.net/11391/151455