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M Zatz

Showing results (151-160 of 252) with videos related to

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European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Thymosin increases production of T-cell growth factor by normal human peripheral blood lymphocytesM M Zatz, J Oliver, C Samuels, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics|August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)A L Sertié, V Sossi, A A Camargo, et al.
Muscle & Nerve|May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathyJ Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|October 1, 1986
Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitutionE R Bortolini, D M da Silva, R S Chequer, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
Psychiatry Research|August 1, 1982
CT measures of cerebrospinal fluid volume in alcoholics and normal volunteersT L Jernigan, L M Zatz, A J Ahumada, et al.
Pageof 26

Showing results (151-160 of 252) with videos related to

Sort By:
Pageof 26
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Thymosin increases production of T-cell growth factor by normal human peripheral blood lymphocytesM M Zatz, J Oliver, C Samuels, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics|August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)A L Sertié, V Sossi, A A Camargo, et al.
Muscle & Nerve|May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathyJ Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|October 1, 1986
Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitutionE R Bortolini, D M da Silva, R S Chequer, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
Psychiatry Research|August 1, 1982
CT measures of cerebrospinal fluid volume in alcoholics and normal volunteersT L Jernigan, L M Zatz, A J Ahumada, et al.
Pageof 26