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C F Hoth

Showing results (1-10 of 7) with videos related to

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Nucleic Acids Research|December 25, 1991
Two RFLPs at the TNP1 locusC F Hoth, W Engel
American Journal of Medical Genetics|August 28, 1995
Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literatureC T Baldwin, C F Hoth, R A Macina, et al.
American Journal of Human Genetics|March 1, 1993
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)C F Hoth, A Milunsky, N Lipsky, et al.
Human Mutation|January 1, 1994
Mutations in PAX3 associated with Waardenburg syndrome type IC T Baldwin, N R Lipsky, C F Hoth, et al.
Nature|February 13, 1992
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndromeC T Baldwin, C F Hoth, J A Amos, et al.
Biochemical and Biophysical Research Communications|April 16, 1998
Expression of the rat adrenomedullin receptor or a putative human adrenomedullin receptor does not correlate with adrenomedullin binding or functional responseS P Kennedy, D Sun, J J Oleynek, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1997
Cloning, expression and pharmacological characterization of rabbit adenosine A1 and A3 receptorsR J Hill, J J Oleynek, C F Hoth, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Nucleic Acids Research|December 25, 1991
Two RFLPs at the TNP1 locusC F Hoth, W Engel
American Journal of Medical Genetics|August 28, 1995
Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literatureC T Baldwin, C F Hoth, R A Macina, et al.
American Journal of Human Genetics|March 1, 1993
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)C F Hoth, A Milunsky, N Lipsky, et al.
Human Mutation|January 1, 1994
Mutations in PAX3 associated with Waardenburg syndrome type IC T Baldwin, N R Lipsky, C F Hoth, et al.
Nature|February 13, 1992
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndromeC T Baldwin, C F Hoth, J A Amos, et al.
Biochemical and Biophysical Research Communications|April 16, 1998
Expression of the rat adrenomedullin receptor or a putative human adrenomedullin receptor does not correlate with adrenomedullin binding or functional responseS P Kennedy, D Sun, J J Oleynek, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1997
Cloning, expression and pharmacological characterization of rabbit adenosine A1 and A3 receptorsR J Hill, J J Oleynek, C F Hoth, et al.
Pageof 1