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S Budde

Showing results (21-30 of 37) with videos related to

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Plos One|December 22, 2006
Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunitySebastian E B Graefe, Thomas Streichert, Birgit S Budde, et al.
Osteoarthritis and Cartilage|August 29, 2021
Do biomarkers allow a differentiation between osteonecrosis of the femoral head and osteoarthritis of the hip? - a biochemical, histological and gene expression analysisT Floerkemeier, S Budde, E Willbold, et al.
FEBS Letters|February 13, 2001
Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndromeS Papa, S Scacco, A M Sardanelli, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 29, 2026
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational familiesDominika Oziębło, Marcin L Leja, Nina Gan, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|July 6, 2010
No effect in combining chondrogenic predifferentiation and mechanical cyclic compression on osteochondral constructs stimulated in a bioreactorS Budde, M Jagodzinski, M Wehmeier, et al.
Archives of Orthopaedic and Trauma Surgery|March 10, 2015
Lumbar lordosis and sacral slope in lumbar spinal stenosis: standard values and measurement accuracyJ Bredow, J Oppermann, M J Scheyerer, et al.
Orphanet Journal of Rare Diseases|June 25, 2015
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasiaKatja Stange, Julie Désir, Naseebullah Kakar, et al.
Journal of Translational Medicine|October 28, 2019
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss geneDominika Oziębło, Anna Sarosiak, Marcin L Leja, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.
Human Genetics|April 21, 2015
Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Plos One|December 22, 2006
Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunitySebastian E B Graefe, Thomas Streichert, Birgit S Budde, et al.
Osteoarthritis and Cartilage|August 29, 2021
Do biomarkers allow a differentiation between osteonecrosis of the femoral head and osteoarthritis of the hip? - a biochemical, histological and gene expression analysisT Floerkemeier, S Budde, E Willbold, et al.
FEBS Letters|February 13, 2001
Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndromeS Papa, S Scacco, A M Sardanelli, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 29, 2026
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational familiesDominika Oziębło, Marcin L Leja, Nina Gan, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|July 6, 2010
No effect in combining chondrogenic predifferentiation and mechanical cyclic compression on osteochondral constructs stimulated in a bioreactorS Budde, M Jagodzinski, M Wehmeier, et al.
Archives of Orthopaedic and Trauma Surgery|March 10, 2015
Lumbar lordosis and sacral slope in lumbar spinal stenosis: standard values and measurement accuracyJ Bredow, J Oppermann, M J Scheyerer, et al.
Orphanet Journal of Rare Diseases|June 25, 2015
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasiaKatja Stange, Julie Désir, Naseebullah Kakar, et al.
Journal of Translational Medicine|October 28, 2019
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss geneDominika Oziębło, Anna Sarosiak, Marcin L Leja, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.
Human Genetics|April 21, 2015
Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
Pageof 4