Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S W Scherer

Showing results (131-140 of 164) with videos related to

Pageof 17
Sort By:
Leukemia|March 9, 2007
Expression and mutation status of candidate kinases in multiple myelomaJ O Claudio, F Zhan, L Zhuang, et al.
Molecular Psychiatry|November 26, 2014
The phenotypic manifestations of rare genic CNVs in autism spectrum disorderA K Merikangas, R Segurado, E A Heron, et al.
Nucleic Acids Research|March 10, 2001
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5M D Wilson, C Riemer, D W Martindale, et al.
The Journal of Biological Chemistry|September 13, 1996
Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in humanJ Rowles, S W Scherer, T Xi, et al.
Genomics|February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.
Nature Genetics|September 6, 2000
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearingA N Smith, J Skaug, K A Choate, et al.
Clinical Genetics|November 23, 2016
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.
Human Molecular Genetics|June 9, 1998
Molecular analysis of the PDS gene in Pendred syndromeB Coyle, W Reardon, J A Herbrick, et al.
Annals of Neurology|February 16, 1999
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyB A Minassian, J Sainz, J M Serratosa, et al.
Nature Genetics|June 16, 1999
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier proteinK Kobayashi, D S Sinasac, M Iijima, et al.
Pageof 17

Showing results (131-140 of 164) with videos related to

Sort By:
Pageof 17
Leukemia|March 9, 2007
Expression and mutation status of candidate kinases in multiple myelomaJ O Claudio, F Zhan, L Zhuang, et al.
Molecular Psychiatry|November 26, 2014
The phenotypic manifestations of rare genic CNVs in autism spectrum disorderA K Merikangas, R Segurado, E A Heron, et al.
Nucleic Acids Research|March 10, 2001
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5M D Wilson, C Riemer, D W Martindale, et al.
The Journal of Biological Chemistry|September 13, 1996
Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in humanJ Rowles, S W Scherer, T Xi, et al.
Genomics|February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.
Nature Genetics|September 6, 2000
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearingA N Smith, J Skaug, K A Choate, et al.
Clinical Genetics|November 23, 2016
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.
Human Molecular Genetics|June 9, 1998
Molecular analysis of the PDS gene in Pendred syndromeB Coyle, W Reardon, J A Herbrick, et al.
Annals of Neurology|February 16, 1999
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyB A Minassian, J Sainz, J M Serratosa, et al.
Nature Genetics|June 16, 1999
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier proteinK Kobayashi, D S Sinasac, M Iijima, et al.
Pageof 17