Human molecular genetics - JoVE Visualize

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Human Molecular Genetics|April 8, 2006

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patientsJelena S Arnold, Evan M Braunstein, Takahiro Ohyama, et al.

Human Molecular Genetics|April 8, 2006

Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegansBrian C Kraemer, Jack K Burgess, Jin H Chen, et al.

Human Molecular Genetics|August 9, 2006

Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factorsJulia K Pinsonneault, Audrey C Papp, Wolfgang Sadée

Human Molecular Genetics|August 9, 2006

Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastomaPaola Ghiorzo, Sara Gargiulo, Lorenza Pastorino, et al.

Human Molecular Genetics|August 9, 2006

Monoamine oxidase A knockout mice exhibit impaired nicotine preference but normal responses to novel stimuliSoh Agatsuma, Moonsook Lee, Hongwen Zhu, et al.

Human Molecular Genetics|August 23, 2006

Variation in MICA and MICB genes and enhanced susceptibility to paucibacillary leprosy in South IndiaKerrie Tosh, Muthuswamy Ravikumar, Jordana Tzenova Bell, et al.

Human Molecular Genetics|August 23, 2006

Conserved distances between vertebrate highly conserved elementsHong Sun, Geir Skogerbø, Runsheng Chen

Human Molecular Genetics|August 23, 2006

Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scanZoe Kemp, Luis Carvajal-Carmona, Sarah Spain, et al.

Human Molecular Genetics|March 1, 2006

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.

Human Molecular Genetics|March 16, 2006

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defectsJayashree Desai, Mark E Shannon, Mahlon D Johnson, et al.

Pageof 1,196

Showing results (401-410 of 11,953) with videos related to

Sort By:

Pageof 1,196

Human Molecular Genetics|April 8, 2006

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patientsJelena S Arnold, Evan M Braunstein, Takahiro Ohyama, et al.

Human Molecular Genetics|April 8, 2006

Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegansBrian C Kraemer, Jack K Burgess, Jin H Chen, et al.

Human Molecular Genetics|August 9, 2006

Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factorsJulia K Pinsonneault, Audrey C Papp, Wolfgang Sadée

Human Molecular Genetics|August 9, 2006

Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastomaPaola Ghiorzo, Sara Gargiulo, Lorenza Pastorino, et al.

Human Molecular Genetics|August 9, 2006

Monoamine oxidase A knockout mice exhibit impaired nicotine preference but normal responses to novel stimuliSoh Agatsuma, Moonsook Lee, Hongwen Zhu, et al.

Human Molecular Genetics|August 23, 2006

Variation in MICA and MICB genes and enhanced susceptibility to paucibacillary leprosy in South IndiaKerrie Tosh, Muthuswamy Ravikumar, Jordana Tzenova Bell, et al.

Human Molecular Genetics|August 23, 2006

Conserved distances between vertebrate highly conserved elementsHong Sun, Geir Skogerbø, Runsheng Chen

Human Molecular Genetics|August 23, 2006

Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scanZoe Kemp, Luis Carvajal-Carmona, Sarah Spain, et al.

Human Molecular Genetics|March 1, 2006

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.

Human Molecular Genetics|March 16, 2006

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defectsJayashree Desai, Mark E Shannon, Mahlon D Johnson, et al.

Pageof 1,196