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U Felbor

Showing results (1-10 of 24) with videos related to

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 27, 1998
[Sorsby's fundus dystrophy. A genetically homogeneous disease]U Felbor, B H Weber
Cytogenetic and Genome Research|October 4, 2003
The rare human fragile site 16BU Felbor, W Feichtinger, M Schmid
Human Mutation|January 1, 1997
Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS geneU Felbor, H Schilling, B H Weber
Zentralblatt Fur Neurochirurgie|September 8, 2006
Genetics of cerebral cavernous angiomaU Felbor, U Sure, T Grimm, et al.
Genome Research|December 1, 1995
Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3)H Stöhr, K Roomp, U Felbor, et al.
Cell Structure and Function|July 8, 2000
Collagen XVIII/endostatin structure and functional role in angiogenesisU K Zatterstrom, U Felbor, N Fukai, et al.
Hamostaseologie|November 6, 2015
Congenital macrothrombocytopenia associated with a combination of functional polymorphisms in the TUBB1 geneJ Stächele, T Bakchoul, J Najm, et al.
The British Journal of Ophthalmology|May 26, 1999
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase geneU Felbor, Y Mutsch, F Grehn, et al.
Investigative Ophthalmology & Visual Science|May 1, 1997
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathiesU Felbor, D Doepner, U Schneider, et al.
FEBS Letters|December 20, 2000
Generation and degradation of human endostatin proteins by various proteinasesM Ferreras, U Felbor, T Lenhard, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 27, 1998
[Sorsby's fundus dystrophy. A genetically homogeneous disease]U Felbor, B H Weber
Cytogenetic and Genome Research|October 4, 2003
The rare human fragile site 16BU Felbor, W Feichtinger, M Schmid
Human Mutation|January 1, 1997
Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS geneU Felbor, H Schilling, B H Weber
Zentralblatt Fur Neurochirurgie|September 8, 2006
Genetics of cerebral cavernous angiomaU Felbor, U Sure, T Grimm, et al.
Genome Research|December 1, 1995
Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3)H Stöhr, K Roomp, U Felbor, et al.
Cell Structure and Function|July 8, 2000
Collagen XVIII/endostatin structure and functional role in angiogenesisU K Zatterstrom, U Felbor, N Fukai, et al.
Hamostaseologie|November 6, 2015
Congenital macrothrombocytopenia associated with a combination of functional polymorphisms in the TUBB1 geneJ Stächele, T Bakchoul, J Najm, et al.
The British Journal of Ophthalmology|May 26, 1999
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase geneU Felbor, Y Mutsch, F Grehn, et al.
Investigative Ophthalmology & Visual Science|May 1, 1997
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathiesU Felbor, D Doepner, U Schneider, et al.
FEBS Letters|December 20, 2000
Generation and degradation of human endostatin proteins by various proteinasesM Ferreras, U Felbor, T Lenhard, et al.
Pageof 3