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N Migone

Showing results (31-40 of 71) with videos related to

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Journal of Medical Genetics|March 1, 1997
Tuberous sclerosis complex: neonatal deaths in three of four children of consanguineous, non-expressing parentsM Ruggieri, C Carbonara, G Magro, et al.
Blood|May 1, 1990
High prevalence of T-cell receptor V delta 2-(D)-D delta 3 or D delta 1/2-D delta 3 rearrangements in B-precursor acute lymphoblastic leukemiasA Biondi, P Francia di Celle, V Rossi, et al.
American Journal of Human Genetics|November 1, 1983
A DNA polymorphism in close physical linkage with the proopiomelanocortin geneJ Feder, N Migone, A C Chang, et al.
Minerva Ginecologica|June 1, 1980
[Prenatal diagnosis. Indications and risks of early amniocentesis by placental puncture and fetoscopy]M Massobrio, F Coppo, F Carozzi, et al.
Contributions to Nephrology|January 1, 1997
A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney diseaseL Longa, A Brusco, C Carbonara, et al.
Human Genetics|April 3, 2001
TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the geneL Longa, A Saluto, A Brusco, et al.
The Journal of Rheumatology. Supplement|January 1, 1977
Family studies and HLA typing in ankylosing spondylitis and sacroiliitisV Daneo, N Migone, V Modena, et al.
The Journal of Experimental Medicine|April 1, 1988
Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte cultureE Ciccone, O Viale, C Bottino, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 5, 1997
A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney diseaseL Longa, F Scolari, A Brusco, et al.
The Journal of Biological Chemistry|November 5, 1999
The SH3 domains of endophilin and amphiphysin bind to the proline-rich region of synaptojanin 1 at distinct sites that display an unconventional binding specificityG Cestra, L Castagnoli, L Dente, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|March 1, 1997
Tuberous sclerosis complex: neonatal deaths in three of four children of consanguineous, non-expressing parentsM Ruggieri, C Carbonara, G Magro, et al.
Blood|May 1, 1990
High prevalence of T-cell receptor V delta 2-(D)-D delta 3 or D delta 1/2-D delta 3 rearrangements in B-precursor acute lymphoblastic leukemiasA Biondi, P Francia di Celle, V Rossi, et al.
American Journal of Human Genetics|November 1, 1983
A DNA polymorphism in close physical linkage with the proopiomelanocortin geneJ Feder, N Migone, A C Chang, et al.
Minerva Ginecologica|June 1, 1980
[Prenatal diagnosis. Indications and risks of early amniocentesis by placental puncture and fetoscopy]M Massobrio, F Coppo, F Carozzi, et al.
Contributions to Nephrology|January 1, 1997
A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney diseaseL Longa, A Brusco, C Carbonara, et al.
Human Genetics|April 3, 2001
TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the geneL Longa, A Saluto, A Brusco, et al.
The Journal of Rheumatology. Supplement|January 1, 1977
Family studies and HLA typing in ankylosing spondylitis and sacroiliitisV Daneo, N Migone, V Modena, et al.
The Journal of Experimental Medicine|April 1, 1988
Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte cultureE Ciccone, O Viale, C Bottino, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 5, 1997
A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney diseaseL Longa, F Scolari, A Brusco, et al.
The Journal of Biological Chemistry|November 5, 1999
The SH3 domains of endophilin and amphiphysin bind to the proline-rich region of synaptojanin 1 at distinct sites that display an unconventional binding specificityG Cestra, L Castagnoli, L Dente, et al.
Pageof 8