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P Leroy

Showing results (271-280 of 438) with videos related to

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Annales De Dermatologie Et De Venereologie|March 5, 2005
[Neutrophilic dermatosis associated with propylthiouracil-induced p-ANCA (p-antineutrophil cytoplasmic antibodies)]A Boulenger-Vazel, I Kupfer-Bessaguet, C Gouedard, et al.
European Journal of Clinical Pharmacology|January 1, 1992
The pharmacokinetics of tiopronin and its principal metabolite (2-mercaptopropionic acid) after oral administration to healthy volunteersB Hercelin, P Leroy, A Nicolas, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 1995
Increased expression in adipocytes of ob RNA in mice with lesions of the hypothalamus and with mutations at the db locusM Maffei, H Fei, G H Lee, et al.
Human Mutation|January 23, 2019
The N-terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bondSarah Naessens, Julie De Zaeytijd, Delfien Syx, et al.
Stem Cell Research|November 6, 2025
Generation and characterization of three human induced pluripotent stem cell lines (UGENTi005, UGENTi006 and UGENTi007) from patients with autosomal dominant adult-onset maculopathy due to RPE65 variant c.1555G>A, p.(E519K)Eline Van Vooren, Filip Van den Broeck, Esperanza Daal, et al.
Survey of Ophthalmology|September 21, 2010
Adult Refsum disease: a form of tapetoretinal dystrophy accessible to therapyKlaus Rüether, Eleanor Baldwin, Minne Casteels, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 29, 2013
Linkage between RFLP markers and genes affecting kernel hardness in wheatP Sourdille, M R Perretant, G Charmet, et al.
Ophthalmic Genetics|March 31, 2016
Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularizationNicole M Fuerst, Leona Serrano, Grace Han, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Pageof 44

Showing results (271-280 of 438) with videos related to

Sort By:
Pageof 44
Annales De Dermatologie Et De Venereologie|March 5, 2005
[Neutrophilic dermatosis associated with propylthiouracil-induced p-ANCA (p-antineutrophil cytoplasmic antibodies)]A Boulenger-Vazel, I Kupfer-Bessaguet, C Gouedard, et al.
European Journal of Clinical Pharmacology|January 1, 1992
The pharmacokinetics of tiopronin and its principal metabolite (2-mercaptopropionic acid) after oral administration to healthy volunteersB Hercelin, P Leroy, A Nicolas, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 1995
Increased expression in adipocytes of ob RNA in mice with lesions of the hypothalamus and with mutations at the db locusM Maffei, H Fei, G H Lee, et al.
Human Mutation|January 23, 2019
The N-terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bondSarah Naessens, Julie De Zaeytijd, Delfien Syx, et al.
Stem Cell Research|November 6, 2025
Generation and characterization of three human induced pluripotent stem cell lines (UGENTi005, UGENTi006 and UGENTi007) from patients with autosomal dominant adult-onset maculopathy due to RPE65 variant c.1555G>A, p.(E519K)Eline Van Vooren, Filip Van den Broeck, Esperanza Daal, et al.
Survey of Ophthalmology|September 21, 2010
Adult Refsum disease: a form of tapetoretinal dystrophy accessible to therapyKlaus Rüether, Eleanor Baldwin, Minne Casteels, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 29, 2013
Linkage between RFLP markers and genes affecting kernel hardness in wheatP Sourdille, M R Perretant, G Charmet, et al.
Ophthalmic Genetics|March 31, 2016
Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularizationNicole M Fuerst, Leona Serrano, Grace Han, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Pageof 44