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Kidney International|November 26, 1999

Spectrum of disease in familial focal and segmental glomerulosclerosisP J Conlon, K Lynn, M P Winn, et al.

Journal of Neuropathology and Experimental Neurology|September 1, 1994

Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic studyS H Han, G Einstein, K H Weisgraber, et al.

Public Health Genomics|May 15, 2009

A Community's Awareness and Perceptions of Genomic MedicineS Hahn, S Letvak, K Powell, et al.

American Journal of Human Genetics|May 1, 1992

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenitaA I McClatchey, J Trofatter, D McKenna-Yasek, et al.

Neurology|July 11, 2006

Paraoxonase cluster polymorphisms are associated with sporadic ALSM Saeed, N Siddique, W Y Hung, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 8, 1994

Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer diseaseW J Strittmatter, A M Saunders, M Goedert, et al.

Genomics|January 25, 2000

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15K B Othmane, E Johnson, M Menold, et al.

Human Molecular Genetics|April 18, 2000

Genome-wide scan for adult onset primary open angle glaucomaJ L Wiggs, R R Allingham, A Hossain, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993

Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer diseaseW J Strittmatter, K H Weisgraber, D Y Huang, et al.

American Journal of Human Genetics|January 1, 1989

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.

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Showing results (11-20 of 31) with videos related to

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Pageof 4

Kidney International|November 26, 1999

Spectrum of disease in familial focal and segmental glomerulosclerosisP J Conlon, K Lynn, M P Winn, et al.

Journal of Neuropathology and Experimental Neurology|September 1, 1994

Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic studyS H Han, G Einstein, K H Weisgraber, et al.

Public Health Genomics|May 15, 2009

A Community's Awareness and Perceptions of Genomic MedicineS Hahn, S Letvak, K Powell, et al.

American Journal of Human Genetics|May 1, 1992

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenitaA I McClatchey, J Trofatter, D McKenna-Yasek, et al.

Neurology|July 11, 2006

Paraoxonase cluster polymorphisms are associated with sporadic ALSM Saeed, N Siddique, W Y Hung, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 8, 1994

Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer diseaseW J Strittmatter, A M Saunders, M Goedert, et al.

Genomics|January 25, 2000

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15K B Othmane, E Johnson, M Menold, et al.

Human Molecular Genetics|April 18, 2000

Genome-wide scan for adult onset primary open angle glaucomaJ L Wiggs, R R Allingham, A Hossain, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993

Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer diseaseW J Strittmatter, K H Weisgraber, D Y Huang, et al.

American Journal of Human Genetics|January 1, 1989

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.

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