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Julia Schmidt

Showing results (91-100 of 147) with videos related to

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Pediatrics|April 22, 2018
Imaging in Pediatric Concussion: A Systematic ReviewJulia Schmidt, Kathryn S Hayward, Katlyn E Brown, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie|May 15, 2023
Quality of Physical Activity Participation Among Adults with Disabilities Through Pandemic RestrictionGordon Tao, Gurkaran Singh, Ethan Simpson, et al.
Journal of Virology|October 17, 2014
Tetramer enrichment reveals the presence of phenotypically diverse hepatitis C virus-specific CD8+ T cells in chronic infectionKatja Nitschke, Tobias Flecken, Julia Schmidt, et al.
Experimental Dermatology|November 11, 2014
Hair follicle targeting, penetration enhancement and Langerhans cell activation make cyanoacrylate skin surface stripping a promising delivery technique for transcutaneous immunization with large molecules and particle-based vaccinesAnnika Vogt, Sabrina Hadam, Iliane Deckert, et al.
Human Molecular Genetics|January 31, 2022
Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signaturesIpek Ilgin Gönenc, Alexander Wolff, Julia Schmidt, et al.
Trials|November 7, 2013
Comparison of error-based and errorless learning for people with severe traumatic brain injury: study protocol for a randomized control trialTamara Ownsworth, Jennifer Fleming, Robyn Tate, et al.
Human Genetics|January 24, 2024
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromesJulia Schmidt, Silke Kaulfuß, Hagen Ott, et al.
European Journal of Human Genetics : EJHG|October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Scientific Reports|March 9, 2022
A novel single-cell RNA-sequencing approach and its applicability connecting genotype to phenotype in ageing diseaseOrr Shomroni, Maren Sitte, Julia Schmidt, et al.
Clinical and Translational Allergy|February 28, 2019
Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedemaAndreas Recke, Elisabeth G Massalme, Uta Jappe, et al.
Pageof 15

Showing results (91-100 of 147) with videos related to

Sort By:
Pageof 15
Pediatrics|April 22, 2018
Imaging in Pediatric Concussion: A Systematic ReviewJulia Schmidt, Kathryn S Hayward, Katlyn E Brown, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie|May 15, 2023
Quality of Physical Activity Participation Among Adults with Disabilities Through Pandemic RestrictionGordon Tao, Gurkaran Singh, Ethan Simpson, et al.
Journal of Virology|October 17, 2014
Tetramer enrichment reveals the presence of phenotypically diverse hepatitis C virus-specific CD8+ T cells in chronic infectionKatja Nitschke, Tobias Flecken, Julia Schmidt, et al.
Experimental Dermatology|November 11, 2014
Hair follicle targeting, penetration enhancement and Langerhans cell activation make cyanoacrylate skin surface stripping a promising delivery technique for transcutaneous immunization with large molecules and particle-based vaccinesAnnika Vogt, Sabrina Hadam, Iliane Deckert, et al.
Human Molecular Genetics|January 31, 2022
Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signaturesIpek Ilgin Gönenc, Alexander Wolff, Julia Schmidt, et al.
Trials|November 7, 2013
Comparison of error-based and errorless learning for people with severe traumatic brain injury: study protocol for a randomized control trialTamara Ownsworth, Jennifer Fleming, Robyn Tate, et al.
Human Genetics|January 24, 2024
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromesJulia Schmidt, Silke Kaulfuß, Hagen Ott, et al.
European Journal of Human Genetics : EJHG|October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Scientific Reports|March 9, 2022
A novel single-cell RNA-sequencing approach and its applicability connecting genotype to phenotype in ageing diseaseOrr Shomroni, Maren Sitte, Julia Schmidt, et al.
Clinical and Translational Allergy|February 28, 2019
Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedemaAndreas Recke, Elisabeth G Massalme, Uta Jappe, et al.
Pageof 15