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J Gitschier

Showing results (31-40 of 84) with videos related to

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American Journal of Human Genetics|May 1, 1994
Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmentiS Das, A Metzenberg, G S Pai, et al.
Current Protocols in Chemical Biology|March 22, 2014
Label-free cell-based dynamic mass redistribution assaysHannah J Gitschier, Audrey B Bergeron, David H Randle
Blood|September 1, 1988
Mutations of factor VIII cleavage sites in hemophilia AJ Gitschier, S Kogan, B Levinson, et al.
Genomics|May 1, 1990
A transcribed gene in an intron of the human factor VIII geneB Levinson, S Kenwrick, D Lakich, et al.
Human Molecular Genetics|June 1, 1992
Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII geneS Kenwrick, B Levinson, S Taylor, et al.
Nature Genetics|October 1, 1992
Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidusY Pan, A Metzenberg, S Das, et al.
Nature Genetics|November 1, 1993
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia AD Lakich, H H Kazazian, S E Antonarakis, et al.
Nature Genetics|January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPaseC Vulpe, B Levinson, S Whitney, et al.
Genomics|August 1, 1992
Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkageC J Faust, B Levinson, J Gitschier, et al.
Nucleic Acids Research|May 11, 1991
A new PstI polymorphism between VK21 and St14 in Xq28 (DXS523)S Kenwrick, P Bridge, D Lillicrap, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1994
Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmentiS Das, A Metzenberg, G S Pai, et al.
Current Protocols in Chemical Biology|March 22, 2014
Label-free cell-based dynamic mass redistribution assaysHannah J Gitschier, Audrey B Bergeron, David H Randle
Blood|September 1, 1988
Mutations of factor VIII cleavage sites in hemophilia AJ Gitschier, S Kogan, B Levinson, et al.
Genomics|May 1, 1990
A transcribed gene in an intron of the human factor VIII geneB Levinson, S Kenwrick, D Lakich, et al.
Human Molecular Genetics|June 1, 1992
Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII geneS Kenwrick, B Levinson, S Taylor, et al.
Nature Genetics|October 1, 1992
Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidusY Pan, A Metzenberg, S Das, et al.
Nature Genetics|November 1, 1993
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia AD Lakich, H H Kazazian, S E Antonarakis, et al.
Nature Genetics|January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPaseC Vulpe, B Levinson, S Whitney, et al.
Genomics|August 1, 1992
Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkageC J Faust, B Levinson, J Gitschier, et al.
Nucleic Acids Research|May 11, 1991
A new PstI polymorphism between VK21 and St14 in Xq28 (DXS523)S Kenwrick, P Bridge, D Lillicrap, et al.
Pageof 9