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The British Journal of Dermatology
|
January 7, 2014
A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration
G Di Zenzo, M El Hachem, A Diociaiuti, et al.
Oncogene
|
April 25, 2012
ADAR2-editing activity inhibits glioblastoma growth through the modulation of the CDC14B/Skp2/p21/p27 axis
F Galeano, C Rossetti, S Tomaselli, et al.
British Heart Journal
|
February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families
E Zachara, A L Caforio, G P Carboni, et al.
Cardiology in the Young
|
July 1, 1999
Tachycardias in children originating in the right ventricular outflow tract: lack of clinical features predicting the presence and severity of the histopathological substrate
F Drago, A Mazza, M G Gagliardi, et al.
Neurology
|
July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27
P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 5, 2000
Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structures
A Teti, S Migliaccio, A Taranta, et al.
Neurology
|
September 12, 2001
Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
S Salvi, F M Santorelli, E Bertini, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 13, 1999
Association of intermediate osteopetrosis with poikiloderma
S Migliaccio, M Luciani, A Taranta, et al.
Cell Death & Disease
|
March 8, 2014
Galectin-3 is a marker of favorable prognosis and a biologically relevant molecule in neuroblastic tumors
V Veschi, M Petroni, A Bartolazzi, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Page
of 12
Search research articles
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Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
The British Journal of Dermatology
|
January 7, 2014
A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration
G Di Zenzo, M El Hachem, A Diociaiuti, et al.
Oncogene
|
April 25, 2012
ADAR2-editing activity inhibits glioblastoma growth through the modulation of the CDC14B/Skp2/p21/p27 axis
F Galeano, C Rossetti, S Tomaselli, et al.
British Heart Journal
|
February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families
E Zachara, A L Caforio, G P Carboni, et al.
Cardiology in the Young
|
July 1, 1999
Tachycardias in children originating in the right ventricular outflow tract: lack of clinical features predicting the presence and severity of the histopathological substrate
F Drago, A Mazza, M G Gagliardi, et al.
Neurology
|
July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27
P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 5, 2000
Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structures
A Teti, S Migliaccio, A Taranta, et al.
Neurology
|
September 12, 2001
Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
S Salvi, F M Santorelli, E Bertini, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 13, 1999
Association of intermediate osteopetrosis with poikiloderma
S Migliaccio, M Luciani, A Taranta, et al.
Cell Death & Disease
|
March 8, 2014
Galectin-3 is a marker of favorable prognosis and a biologically relevant molecule in neuroblastic tumors
V Veschi, M Petroni, A Bartolazzi, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Page
of 12