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S Ciarmatori

Showing results (1-10 of 6) with videos related to

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Trends in Genetics : TIG|November 1, 1996
A new method to screen clones from differential display experiments prior to RNA studiesG G Consalez, A Corradi, S Ciarmatori, et al.
The Journal of Biological Chemistry|July 11, 1997
Mmot1, a new helix-loop-helix transcription factor gene displaying a sharp expression boundary in the embryonic mouse brainN Malgaretti, O Pozzoli, A Bosetti, et al.
Pediatric Research|August 14, 1999
Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome?A Bettinelli, R Rusconi, S Ciarmatori, et al.
Molecular and Cellular Biology|August 4, 2001
Overlapping functions of the pRb family in the regulation of rRNA synthesisS Ciarmatori, P H Scott, J E Sutcliffe, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Phenotypic variability in Bartter syndrome type IA Bettinelli, S Ciarmatori, L Cesareo, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Trends in Genetics : TIG|November 1, 1996
A new method to screen clones from differential display experiments prior to RNA studiesG G Consalez, A Corradi, S Ciarmatori, et al.
The Journal of Biological Chemistry|July 11, 1997
Mmot1, a new helix-loop-helix transcription factor gene displaying a sharp expression boundary in the embryonic mouse brainN Malgaretti, O Pozzoli, A Bosetti, et al.
Pediatric Research|August 14, 1999
Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome?A Bettinelli, R Rusconi, S Ciarmatori, et al.
Molecular and Cellular Biology|August 4, 2001
Overlapping functions of the pRb family in the regulation of rRNA synthesisS Ciarmatori, P H Scott, J E Sutcliffe, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Phenotypic variability in Bartter syndrome type IA Bettinelli, S Ciarmatori, L Cesareo, et al.
Pageof 1