A Lunkes|J L Mandel - JoVE Visualize

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Proceedings of the National Academy of Sciences of the United States of America|April 1, 1992

Adenovirus as an expression vector in muscle cells in vivoB Quantin, L D Perricaudet, S Tajbakhsh, et al.

Nucleic Acids Research|August 12, 1985

Homologies between X and Y chromosomes detected by DNA probes: localisation and evolutionM Koenig, J P Moisan, R Heilig, et al.

Trends in Genetics : TIG|March 29, 2001

The myotubularin family: from genetic disease to phosphoinositide metabolismJ Laporte, F Blondeau, A Buj-Bello, et al.

Human Molecular Genetics|July 1, 1997

Transition from premutation to full mutation in fragile X syndrome is likely to be prezygoticC Moutou, M C Vincent, V Biancalana, et al.

Cellular and Molecular Life Sciences : CMLS|November 18, 2003

Implication of phosphoinositide phosphatases in genetic diseases: the case of myotubularinH Tronchère, A Buj-Bello, J-L Mandel, et al.

Human Genetics|February 1, 1986

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.

Journal of Medical Genetics|November 1, 1992

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.

Revue Neurologique|December 19, 2000

[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.

Human Molecular Genetics|June 1, 1994

The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.

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Showing results (41-50 of 198) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 1, 1992

Adenovirus as an expression vector in muscle cells in vivoB Quantin, L D Perricaudet, S Tajbakhsh, et al.

Nucleic Acids Research|August 12, 1985

Homologies between X and Y chromosomes detected by DNA probes: localisation and evolutionM Koenig, J P Moisan, R Heilig, et al.

Trends in Genetics : TIG|March 29, 2001

The myotubularin family: from genetic disease to phosphoinositide metabolismJ Laporte, F Blondeau, A Buj-Bello, et al.

Human Molecular Genetics|July 1, 1997

Transition from premutation to full mutation in fragile X syndrome is likely to be prezygoticC Moutou, M C Vincent, V Biancalana, et al.

Cellular and Molecular Life Sciences : CMLS|November 18, 2003

Implication of phosphoinositide phosphatases in genetic diseases: the case of myotubularinH Tronchère, A Buj-Bello, J-L Mandel, et al.

Human Genetics|February 1, 1986

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.

Journal of Medical Genetics|November 1, 1992

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.

Revue Neurologique|December 19, 2000

[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.

Human Molecular Genetics|June 1, 1994

The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.

Pageof 20