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D Weil

Showing results (191-200 of 203) with videos related to

Pageof 21
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Medical Physics|August 14, 2021
Dosimetry of a novel converging X-ray source for kilovoltage radiotherapyTyler Stalbaum, Larry Partain, Michael D Weil, et al.
Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Stem Cell Research & Therapy|June 27, 2020
Lung delivery of MSCs expressing anti-cancer protein TRAIL visualised with <sup>89</sup>Zr-oxine PET-CTP Stephen Patrick, Krishna K Kolluri, May Zaw Thin, et al.
Human Molecular Genetics|January 1, 1997
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IBG Lévy, F Levi-Acobas, S Blanchard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982
Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.
Progress in Clinical and Biological Research|January 1, 1982
Workshop on mapping by somatic cell hybridizationF H Ruddle, D Bootsma, M Stefani, et al.
The Journal of Chemical Physics|August 9, 2024
First-principles investigation of oxidized Si- and Ge-terminated diamond (100) surfacesH Gomez, J Cruz, C Milne, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 21

Showing results (191-200 of 203) with videos related to

Sort By:
Pageof 21
Medical Physics|August 14, 2021
Dosimetry of a novel converging X-ray source for kilovoltage radiotherapyTyler Stalbaum, Larry Partain, Michael D Weil, et al.
Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Stem Cell Research & Therapy|June 27, 2020
Lung delivery of MSCs expressing anti-cancer protein TRAIL visualised with <sup>89</sup>Zr-oxine PET-CTP Stephen Patrick, Krishna K Kolluri, May Zaw Thin, et al.
Human Molecular Genetics|January 1, 1997
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IBG Lévy, F Levi-Acobas, S Blanchard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982
Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.
Progress in Clinical and Biological Research|January 1, 1982
Workshop on mapping by somatic cell hybridizationF H Ruddle, D Bootsma, M Stefani, et al.
The Journal of Chemical Physics|August 9, 2024
First-principles investigation of oxidized Si- and Ge-terminated diamond (100) surfacesH Gomez, J Cruz, C Milne, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 21