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Trends in Genetics : TIG
|
November 1, 1996
A new method to screen clones from differential display experiments prior to RNA studies
G 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 brain
N 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 synthesis
S 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 metalloprotease
G Casari, M De Fusco, S Ciarmatori, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 7, 2000
Phenotypic variability in Bartter syndrome type I
A Bettinelli, S Ciarmatori, L Cesareo, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Trends in Genetics : TIG
|
November 1, 1996
A new method to screen clones from differential display experiments prior to RNA studies
G 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 brain
N 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 synthesis
S 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 metalloprotease
G Casari, M De Fusco, S Ciarmatori, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 7, 2000
Phenotypic variability in Bartter syndrome type I
A Bettinelli, S Ciarmatori, L Cesareo, et al.
Page
of 1