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P Aula

Showing results (151-160 of 161) with videos related to

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Parasitology|August 25, 2020
Molecular identification of <i>Ancylostoma ceylanicum</i> in the PhilippinesOyime P Aula, Donald P McManus, Kosala G Weerakoon, et al.
Human Genetics|July 1, 1997
Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intoleranceT Lauteala, N Horelli-Kuitunen, E Closs, et al.
Human Mutation|June 20, 1998
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathiesK Silander, P Meretoja, V Juvonen, et al.
Kidney International|March 1, 1997
Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysisM Männikkö, M Kestilä, U Lenkkeri, et al.
American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.
Pediatric Neurology|May 7, 2002
Phenotypic spectrum of Salla disease, a free sialic acid storage disorderTarja T Varho, Liisa E Alajoki, Kristiina M Posti, et al.
Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Human Molecular Genetics|February 3, 2000
Functional analysis of novel mutations in y(+)LAT-1 amino acid transporter gene causing lysinuric protein intolerance (LPI)J Mykkänen, D Torrents, M Pineda, et al.
Nature Genetics|March 18, 1999
Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance geneD Torrents, J Mykkänen, M Pineda, et al.
Pageof 17

Showing results (151-160 of 161) with videos related to

Sort By:
Pageof 17
Parasitology|August 25, 2020
Molecular identification of <i>Ancylostoma ceylanicum</i> in the PhilippinesOyime P Aula, Donald P McManus, Kosala G Weerakoon, et al.
Human Genetics|July 1, 1997
Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intoleranceT Lauteala, N Horelli-Kuitunen, E Closs, et al.
Human Mutation|June 20, 1998
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathiesK Silander, P Meretoja, V Juvonen, et al.
Kidney International|March 1, 1997
Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysisM Männikkö, M Kestilä, U Lenkkeri, et al.
American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.
Pediatric Neurology|May 7, 2002
Phenotypic spectrum of Salla disease, a free sialic acid storage disorderTarja T Varho, Liisa E Alajoki, Kristiina M Posti, et al.
Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Human Molecular Genetics|February 3, 2000
Functional analysis of novel mutations in y(+)LAT-1 amino acid transporter gene causing lysinuric protein intolerance (LPI)J Mykkänen, D Torrents, M Pineda, et al.
Nature Genetics|March 18, 1999
Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance geneD Torrents, J Mykkänen, M Pineda, et al.
Pageof 17