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G LeRoy

Showing results (301-310 of 316) with videos related to

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Human Molecular Genetics|January 1, 1997
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlationsJ Meyer, P Südbeck, M Held, et al.
Oncogene|September 15, 2010
BCR-ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patientsD D De Carvalho, R Binato, W O Pereira, et al.
Molecular Genetics and Metabolism|May 5, 2016
New observation of sialuria prompts detection of liver tumor in previously reported patientNeena L Champaigne, Jules G Leroy, Priya S Kishnani, et al.
Biochemical and Biophysical Research Communications|November 9, 2005
Aminoacylase I deficiency: a novel inborn error of metabolismR N Van Coster, E A Gerlo, T G Giardina, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Journal of Neuro-Oncology|May 17, 2018
Virus vector-mediated genetic modification of brain tumor stromal cells after intravenous deliveryAdrienn Volak, Stanley G LeRoy, Jeya Shree Natasan, et al.
Clinical Dysmorphology|December 4, 2018
Does the clinical phenotype of mucolipidosis-IIIγ differ from its αβ counterpart?: supporting facts in a cohort of 18 patientsSheela Nampoothiri, Nursel H Elcioglu, Suleyman S Koca, et al.
Science Translational Medicine|April 11, 2014
Sustained normalization of neurological disease after intracranial gene therapy in a feline modelVictoria J McCurdy, Aime K Johnson, Heather L Gray-Edwards, et al.
Cold Spring Harbor Symposia on Quantitative Biology|June 29, 1999
The RNA polymerase II general transcription factors: past, present, and futureD Reinberg, G Orphanides, R Ebright, et al.
Nature Genetics|February 28, 2006
Mutations in different components of FGF signaling in LADD syndromeEdyta Rohmann, Han G Brunner, Hülya Kayserili, et al.
Pageof 32

Showing results (301-310 of 316) with videos related to

Sort By:
Pageof 32
Human Molecular Genetics|January 1, 1997
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlationsJ Meyer, P Südbeck, M Held, et al.
Oncogene|September 15, 2010
BCR-ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patientsD D De Carvalho, R Binato, W O Pereira, et al.
Molecular Genetics and Metabolism|May 5, 2016
New observation of sialuria prompts detection of liver tumor in previously reported patientNeena L Champaigne, Jules G Leroy, Priya S Kishnani, et al.
Biochemical and Biophysical Research Communications|November 9, 2005
Aminoacylase I deficiency: a novel inborn error of metabolismR N Van Coster, E A Gerlo, T G Giardina, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Journal of Neuro-Oncology|May 17, 2018
Virus vector-mediated genetic modification of brain tumor stromal cells after intravenous deliveryAdrienn Volak, Stanley G LeRoy, Jeya Shree Natasan, et al.
Clinical Dysmorphology|December 4, 2018
Does the clinical phenotype of mucolipidosis-IIIγ differ from its αβ counterpart?: supporting facts in a cohort of 18 patientsSheela Nampoothiri, Nursel H Elcioglu, Suleyman S Koca, et al.
Science Translational Medicine|April 11, 2014
Sustained normalization of neurological disease after intracranial gene therapy in a feline modelVictoria J McCurdy, Aime K Johnson, Heather L Gray-Edwards, et al.
Cold Spring Harbor Symposia on Quantitative Biology|June 29, 1999
The RNA polymerase II general transcription factors: past, present, and futureD Reinberg, G Orphanides, R Ebright, et al.
Nature Genetics|February 28, 2006
Mutations in different components of FGF signaling in LADD syndromeEdyta Rohmann, Han G Brunner, Hülya Kayserili, et al.
Pageof 32