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F L Munier

Showing results (21-30 of 59) with videos related to

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 7, 2005
Keratoepithelin in secondary corneal amyloidosisD Suesskind, C Auw-Haedrich, D F Schorderet, et al.
The British Journal of Ophthalmology|October 24, 2006
Exclusion of COL8A1, the gene encoding the alpha2(VIII) chain of type VIII collagen, as a candidate for Fuchs endothelial dystrophy and posterior polymorphous corneal dystrophyJ E Urquhart, S Biswas, G C M Black, et al.
Case Reports in Ophthalmological Medicine|August 2, 2023
Retinocytoma Undergoing Retinoblastoma Transformation in an Adult PatientJ Navaratnam, R Faber, N Eide, et al.
Ophthalmic Genetics|March 23, 2001
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomaliesL Lavanchy, F L Munier, P Cousin, et al.
BMC Cancer|September 2, 2025
Spatial transcriptomics of retinoblastoma: a visual window on intra-patient heterogeneityA P Moulin, J Thevenet, L Mazzeo, et al.
The Journal of Biological Chemistry|February 7, 2001
Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the proteinE Korvatska, H Henry, Y Mashima, et al.
Ophthalmic Genetics|July 15, 2000
Haplotye analysis of Jaanese families with a superficial variant of granular corneal dystrohy: evidence for multiple origins of R124L mutation of keratoepithelinE Korvatska, M Yamada, S Yamamoto, et al.
Nature Genetics|March 1, 1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesF L Munier, E Korvatska, A Djemaï, et al.
The British Journal of Ophthalmology|July 20, 2007
De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophyE N Hilton, G C M Black, F D C Manson, et al.
American Journal of Human Genetics|October 16, 1999
The gamma-crystallins and human cataracts: a puzzle made clearerE Héon, M Priston, D F Schorderet, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 7, 2005
Keratoepithelin in secondary corneal amyloidosisD Suesskind, C Auw-Haedrich, D F Schorderet, et al.
The British Journal of Ophthalmology|October 24, 2006
Exclusion of COL8A1, the gene encoding the alpha2(VIII) chain of type VIII collagen, as a candidate for Fuchs endothelial dystrophy and posterior polymorphous corneal dystrophyJ E Urquhart, S Biswas, G C M Black, et al.
Case Reports in Ophthalmological Medicine|August 2, 2023
Retinocytoma Undergoing Retinoblastoma Transformation in an Adult PatientJ Navaratnam, R Faber, N Eide, et al.
Ophthalmic Genetics|March 23, 2001
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomaliesL Lavanchy, F L Munier, P Cousin, et al.
BMC Cancer|September 2, 2025
Spatial transcriptomics of retinoblastoma: a visual window on intra-patient heterogeneityA P Moulin, J Thevenet, L Mazzeo, et al.
The Journal of Biological Chemistry|February 7, 2001
Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the proteinE Korvatska, H Henry, Y Mashima, et al.
Ophthalmic Genetics|July 15, 2000
Haplotye analysis of Jaanese families with a superficial variant of granular corneal dystrohy: evidence for multiple origins of R124L mutation of keratoepithelinE Korvatska, M Yamada, S Yamamoto, et al.
Nature Genetics|March 1, 1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesF L Munier, E Korvatska, A Djemaï, et al.
The British Journal of Ophthalmology|July 20, 2007
De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophyE N Hilton, G C M Black, F D C Manson, et al.
American Journal of Human Genetics|October 16, 1999
The gamma-crystallins and human cataracts: a puzzle made clearerE Héon, M Priston, D F Schorderet, et al.
Pageof 6