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C Sobacchi

Showing results (1-10 of 14) with videos related to

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Current Opinion in Allergy and Clinical Immunology|April 20, 2002
Recombination activating gene and its defectsA Villa, C Sobacchi, P Vezzoni
Immunological Reviews|February 24, 2001
The genetic and biochemical basis of Omenn syndromeS Santagata, A Villa, C Sobacchi, et al.
Journal of Endocrinological Investigation|January 12, 2022
Direct effects of octreotide on osteoblast cell proliferation and functionE Vitali, E Palagano, M L Schiavone, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of RAG-deficient Omenn syndromeA Villa, F Bozzi, C Sobacchi, et al.
Journal of Endocrinological Investigation|December 30, 2023
The direct impact of pegvisomant on osteoblast functions and bone developmentE Vitali, A Grasso, M L Schiavone, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 11, 2012
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implicationsA Pangrazio, M E Caldana, N Lo Iacono, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domainsS Santagata, C A Gomez, C Sobacchi, et al.
Molecular Cell|January 15, 2000
The RAG1/RAG2 complex constitutes a 3' flap endonuclease: implications for junctional diversity in V(D)J and transpositional recombinationS Santagata, E Besmer, A Villa, et al.
Calcified Tissue International|October 3, 2003
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in womenC Sobacchi, P Vezzoni, D M Reid, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Current Opinion in Allergy and Clinical Immunology|April 20, 2002
Recombination activating gene and its defectsA Villa, C Sobacchi, P Vezzoni
Immunological Reviews|February 24, 2001
The genetic and biochemical basis of Omenn syndromeS Santagata, A Villa, C Sobacchi, et al.
Journal of Endocrinological Investigation|January 12, 2022
Direct effects of octreotide on osteoblast cell proliferation and functionE Vitali, E Palagano, M L Schiavone, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of RAG-deficient Omenn syndromeA Villa, F Bozzi, C Sobacchi, et al.
Journal of Endocrinological Investigation|December 30, 2023
The direct impact of pegvisomant on osteoblast functions and bone developmentE Vitali, A Grasso, M L Schiavone, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 11, 2012
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implicationsA Pangrazio, M E Caldana, N Lo Iacono, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domainsS Santagata, C A Gomez, C Sobacchi, et al.
Molecular Cell|January 15, 2000
The RAG1/RAG2 complex constitutes a 3' flap endonuclease: implications for junctional diversity in V(D)J and transpositional recombinationS Santagata, E Besmer, A Villa, et al.
Calcified Tissue International|October 3, 2003
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in womenC Sobacchi, P Vezzoni, D M Reid, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
Pageof 2