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Steffen Uebe

Showing results (71-80 of 88) with videos related to

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Nature Genetics|October 19, 2010
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasisUlrike Hüffmeier, Steffen Uebe, Arif B Ekici, et al.
American Journal of Human Genetics|December 7, 2015
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8Kym M Boycott, Chandree L Beaulieu, Kristin D Kernohan, et al.
JAMA Psychiatry|January 19, 2017
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental DisordersMiriam S Reuter, Hasan Tawamie, Rebecca Buchert, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Communications|February 6, 2015
Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritisJohn Bowes, Ashley Budu-Aggrey, Ulrike Huffmeier, et al.
Kidney International|June 1, 2022
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseasesFlorian J Wopperer, Karl X Knaup, Kira J Stanzick, et al.
Nature|February 1, 2019
PU.1 controls fibroblast polarization and tissue fibrosisThomas Wohlfahrt, Simon Rauber, Steffen Uebe, et al.
American Journal of Human Genetics|August 8, 2020
Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin DiseasesStefan Haskamp, Heiko Bruns, Madelaine Hahn, et al.
Human Mutation|June 18, 2010
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrumVerena Matejas, Bernward Hinkes, Faisal Alkandari, et al.
Human Molecular Genetics|August 27, 2015
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locusMichael A Hauser, Inas F Aboobakar, Yutao Liu, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Nature Genetics|October 19, 2010
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasisUlrike Hüffmeier, Steffen Uebe, Arif B Ekici, et al.
American Journal of Human Genetics|December 7, 2015
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8Kym M Boycott, Chandree L Beaulieu, Kristin D Kernohan, et al.
JAMA Psychiatry|January 19, 2017
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental DisordersMiriam S Reuter, Hasan Tawamie, Rebecca Buchert, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Communications|February 6, 2015
Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritisJohn Bowes, Ashley Budu-Aggrey, Ulrike Huffmeier, et al.
Kidney International|June 1, 2022
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseasesFlorian J Wopperer, Karl X Knaup, Kira J Stanzick, et al.
Nature|February 1, 2019
PU.1 controls fibroblast polarization and tissue fibrosisThomas Wohlfahrt, Simon Rauber, Steffen Uebe, et al.
American Journal of Human Genetics|August 8, 2020
Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin DiseasesStefan Haskamp, Heiko Bruns, Madelaine Hahn, et al.
Human Mutation|June 18, 2010
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrumVerena Matejas, Bernward Hinkes, Faisal Alkandari, et al.
Human Molecular Genetics|August 27, 2015
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locusMichael A Hauser, Inas F Aboobakar, Yutao Liu, et al.
Pageof 9