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A Ciccodicola

Showing results (31-40 of 47) with videos related to

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Gene|August 5, 2000
Human dbl proto-oncogene in 85 kb of xq26, and determination of the transcription initiation siteG Palmieri, V de Franciscis, A Casamassimi, et al.
Gene|November 24, 1999
Human and mouse SYBL1 gene structure and expressionM R Matarazzo, M Cuccurese, M Strazzullo, et al.
Journal of Medical Genetics|July 5, 2005
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian familiesC Ziviello, F Simonelli, F Testa, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of delta7-sterol reductase in Italy and report of three novel mutationsD De Brasi, T Esposito, M Rossi, et al.
International Journal of Obesity (2005)|March 17, 2016
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat dietL Parrillo, V Costa, G A Raciti, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Human Molecular Genetics|September 25, 1997
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.
Clinical Genetics|November 27, 1998
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneityG de Crecchio, F Simonelli, G Nunziata, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Gene|August 5, 2000
Human dbl proto-oncogene in 85 kb of xq26, and determination of the transcription initiation siteG Palmieri, V de Franciscis, A Casamassimi, et al.
Gene|November 24, 1999
Human and mouse SYBL1 gene structure and expressionM R Matarazzo, M Cuccurese, M Strazzullo, et al.
Journal of Medical Genetics|July 5, 2005
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian familiesC Ziviello, F Simonelli, F Testa, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of delta7-sterol reductase in Italy and report of three novel mutationsD De Brasi, T Esposito, M Rossi, et al.
International Journal of Obesity (2005)|March 17, 2016
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat dietL Parrillo, V Costa, G A Raciti, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Human Molecular Genetics|September 25, 1997
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.
Clinical Genetics|November 27, 1998
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneityG de Crecchio, F Simonelli, G Nunziata, et al.
Pageof 5