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P Monaco

Showing results (571-580 of 719) with videos related to

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Genomics|March 1, 1994
Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell linesF Francis, F Benham, C G See, et al.
Human Mutation|October 17, 2006
Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative casesLorne Lonie, Daniel E Porter, Maria Fraser, et al.
Cancer|April 1, 1993
American Cancer Society Workshop on Adolescents and Young Adults with Cancer. Workgroup #2: Insurance and employabilityR J McKenna, B Black, R Hughes, et al.
Genomics|April 1, 1988
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneM Burmeister, A P Monaco, E F Gillard, et al.
Nature Genetics|June 1, 1992
Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate regionG P Bates, J Valdes, H Hummerich, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
The Journal of Investigative Dermatology|February 14, 2002
Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 geneCarol Dobson-Stone, Rebecca Fairclough, Eimear Dunne, et al.
Transplantation Proceedings|February 1, 1991
The biohybrid artificial pancreas for treatment of diabetes in totally pancreatectomized dogsT Maki, C S Ubhi, H Sanchez-Farpon, et al.
Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Nature Genetics|May 1, 1996
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndromeE Maestrini, A P Monaco, J A McGrath, et al.
Pageof 72

Showing results (571-580 of 719) with videos related to

Sort By:
Pageof 72
Genomics|March 1, 1994
Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell linesF Francis, F Benham, C G See, et al.
Human Mutation|October 17, 2006
Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative casesLorne Lonie, Daniel E Porter, Maria Fraser, et al.
Cancer|April 1, 1993
American Cancer Society Workshop on Adolescents and Young Adults with Cancer. Workgroup #2: Insurance and employabilityR J McKenna, B Black, R Hughes, et al.
Genomics|April 1, 1988
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneM Burmeister, A P Monaco, E F Gillard, et al.
Nature Genetics|June 1, 1992
Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate regionG P Bates, J Valdes, H Hummerich, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
The Journal of Investigative Dermatology|February 14, 2002
Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 geneCarol Dobson-Stone, Rebecca Fairclough, Eimear Dunne, et al.
Transplantation Proceedings|February 1, 1991
The biohybrid artificial pancreas for treatment of diabetes in totally pancreatectomized dogsT Maki, C S Ubhi, H Sanchez-Farpon, et al.
Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Nature Genetics|May 1, 1996
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndromeE Maestrini, A P Monaco, J A McGrath, et al.
Pageof 72