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P Leroy

Showing results (281-290 of 438) with videos related to

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Cancer Gene Therapy|May 3, 2001
Regression of primary hepatocarcinoma in cancer-prone transgenic mice by local interferon-gamma delivery is associated with macrophages recruitment and nitric oxide productionM Baratin, M Ziol, R Romieu, et al.
Retina (Philadelphia, Pa.)|April 27, 2013
High-resolution optical coherence tomography, autofluorescence, and infrared reflectance imaging in Sjögren reticular dystrophyPieter-Paul Schauwvlieghe, Kara Della Torre, Frauke Coppieters, et al.
Infectious Diseases Now|February 11, 2023
Management of imported malaria in the emergency department: Adequacy compared to guidelines, and impact of the SARS-CoV-2 pandemicC Flateau, A Pitsch, C Cornaglia, et al.
Genome|April 1, 1996
Molecular genetic maps of the group 6 chromosomes of hexaploid wheat (Triticum aestivum L. em. Thell.)C L Marino, N A Tuleen, G E Hart, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 14, 2011
Insights into levator muscle dysfunction in a cohort of patients with molecularly confirmed blepharophimosis-ptosis-epicanthus inversus syndrome using high-resolution imaging, anatomic examination, and histopathologic examinationChristian E Decock, Elfride E De Baere, Wouter Bauters, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 7, 2015
Haplotype divergence and multiple candidate genes at Rphq2, a partial resistance QTL of barley to Puccinia hordeiF K S Yeo, Y Wang, T Vozabova, et al.
Ophthalmic Genetics|May 21, 2021
Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in <i>ASPH</i>Tom Van Hoorde, Fanny Nerinckx, Elke Kreps, et al.
American Journal of Human Genetics|June 15, 2007
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosaFrauke Coppieters, Bart P Leroy, Diane Beysen, et al.
Molecular Vision|October 25, 2017
The importance of genetic testing as demonstrated by two cases of <i>CACNA1F</i>-associated retinal generation misdiagnosed as LCAClara J Men, Kinga M Bujakowska, Jason Comander, et al.
Pageof 44

Showing results (281-290 of 438) with videos related to

Sort By:
Pageof 44
Cancer Gene Therapy|May 3, 2001
Regression of primary hepatocarcinoma in cancer-prone transgenic mice by local interferon-gamma delivery is associated with macrophages recruitment and nitric oxide productionM Baratin, M Ziol, R Romieu, et al.
Retina (Philadelphia, Pa.)|April 27, 2013
High-resolution optical coherence tomography, autofluorescence, and infrared reflectance imaging in Sjögren reticular dystrophyPieter-Paul Schauwvlieghe, Kara Della Torre, Frauke Coppieters, et al.
Infectious Diseases Now|February 11, 2023
Management of imported malaria in the emergency department: Adequacy compared to guidelines, and impact of the SARS-CoV-2 pandemicC Flateau, A Pitsch, C Cornaglia, et al.
Genome|April 1, 1996
Molecular genetic maps of the group 6 chromosomes of hexaploid wheat (Triticum aestivum L. em. Thell.)C L Marino, N A Tuleen, G E Hart, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 14, 2011
Insights into levator muscle dysfunction in a cohort of patients with molecularly confirmed blepharophimosis-ptosis-epicanthus inversus syndrome using high-resolution imaging, anatomic examination, and histopathologic examinationChristian E Decock, Elfride E De Baere, Wouter Bauters, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 7, 2015
Haplotype divergence and multiple candidate genes at Rphq2, a partial resistance QTL of barley to Puccinia hordeiF K S Yeo, Y Wang, T Vozabova, et al.
Ophthalmic Genetics|May 21, 2021
Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in <i>ASPH</i>Tom Van Hoorde, Fanny Nerinckx, Elke Kreps, et al.
American Journal of Human Genetics|June 15, 2007
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosaFrauke Coppieters, Bart P Leroy, Diane Beysen, et al.
Molecular Vision|October 25, 2017
The importance of genetic testing as demonstrated by two cases of <i>CACNA1F</i>-associated retinal generation misdiagnosed as LCAClara J Men, Kinga M Bujakowska, Jason Comander, et al.
Pageof 44