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Rolfs

Showing results (551-560 of 632) with videos related to

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Neurology|November 5, 2013
MRI in acute cerebral ischemia of the young: the Stroke in Young Fabry Patients (sifap1) StudyFranz Fazekas, Christian Enzinger, Reinhold Schmidt, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
X-linked Dystonia-Parkinsonism manifesting in a female patient due to atypical turner syndromeAna Westenberger, Raymond L Rosales, Sascha Heinitz, et al.
Clinical Genetics|December 17, 2009
Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosisM Griese, F Brasch, V R Aldana, et al.
The Biochemical Journal|January 4, 2020
Proteostasis regulators modulate proteasomal activity and gene expression to attenuate multiple phenotypes in Fabry diseaseSusanne Seemann, Mathias Ernst, Chiara Cimmaruta, et al.
Plos One|January 31, 2008
A biomedically enriched collection of 7000 human ORF clonesAndreas Rolfs, Yanhui Hu, Lars Ebert, et al.
Science (New York, N.Y.)|March 7, 2001
An iron-regulated ferric reductase associated with the absorption of dietary ironA T McKie, D Barrow, G O Latunde-Dada, et al.
Parkinsonism & Related Disorders|August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative casesAi Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
Physical Review Letters|August 8, 2009
Stellar and primordial nucleosynthesis of 7Be: measurement of 3He(alpha,gamma)7BeA Di Leva, L Gialanella, R Kunz, et al.
Stroke|December 1, 2016
Patent Foramen Ovale and Cryptogenic Strokes in the Stroke in Young Fabry Patients StudyRoman Huber, Ulrike Grittner, Frank Weidemann, et al.
Human Molecular Genetics|January 15, 2017
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humansKatja Lohmann, Ikuo Masuho, Dipak N Patil, et al.
Pageof 64

Showing results (551-560 of 632) with videos related to

Sort By:
Pageof 64
Neurology|November 5, 2013
MRI in acute cerebral ischemia of the young: the Stroke in Young Fabry Patients (sifap1) StudyFranz Fazekas, Christian Enzinger, Reinhold Schmidt, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
X-linked Dystonia-Parkinsonism manifesting in a female patient due to atypical turner syndromeAna Westenberger, Raymond L Rosales, Sascha Heinitz, et al.
Clinical Genetics|December 17, 2009
Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosisM Griese, F Brasch, V R Aldana, et al.
The Biochemical Journal|January 4, 2020
Proteostasis regulators modulate proteasomal activity and gene expression to attenuate multiple phenotypes in Fabry diseaseSusanne Seemann, Mathias Ernst, Chiara Cimmaruta, et al.
Plos One|January 31, 2008
A biomedically enriched collection of 7000 human ORF clonesAndreas Rolfs, Yanhui Hu, Lars Ebert, et al.
Science (New York, N.Y.)|March 7, 2001
An iron-regulated ferric reductase associated with the absorption of dietary ironA T McKie, D Barrow, G O Latunde-Dada, et al.
Parkinsonism & Related Disorders|August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative casesAi Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
Physical Review Letters|August 8, 2009
Stellar and primordial nucleosynthesis of 7Be: measurement of 3He(alpha,gamma)7BeA Di Leva, L Gialanella, R Kunz, et al.
Stroke|December 1, 2016
Patent Foramen Ovale and Cryptogenic Strokes in the Stroke in Young Fabry Patients StudyRoman Huber, Ulrike Grittner, Frank Weidemann, et al.
Human Molecular Genetics|January 15, 2017
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humansKatja Lohmann, Ikuo Masuho, Dipak N Patil, et al.
Pageof 64