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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 immunity
Sebastian 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 analysis
T 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 syndrome
S 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 families
Dominika 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 bioreactor
S 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 accuracy
J Bredow, J Oppermann, M J Scheyerer, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2015
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia
Katja 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 gene
Dominika 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 I
S 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 B3GAT3
Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
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Search research articles
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Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 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 immunity
Sebastian 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 analysis
T 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 syndrome
S 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 families
Dominika 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 bioreactor
S 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 accuracy
J Bredow, J Oppermann, M J Scheyerer, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2015
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia
Katja 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 gene
Dominika 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 I
S 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 B3GAT3
Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
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of 4