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Michael Ludwig

Showing results (161-170 of 239) with videos related to

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Molecular Medicine Reports|March 18, 2015
Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouseNirmala Gurung, Greta Grosse, Markus Draaken, et al.
Frontiers in Medicine|December 11, 2023
A blended learning approach for teaching thoracic radiology to medical students: a proof-of-concept studyFabian Stoehr, Yang Yang, Lukas Müller, et al.
International Journal of Molecular Medicine|November 3, 2010
p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissueBonnie J Ching, Lars Wittler, Judith Proske, et al.
Journal of Neurodevelopmental Disorders|April 19, 2016
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVsMadita Schumann, Andrea Hofmann, Sophia K Krutzke, et al.
Birth Defects Research|March 20, 2019
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrumFranziska Kause, Rong Zhang, Michael Ludwig, et al.
Journal of Neurochemistry|April 2, 2004
Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry studyStephan Steckelbroeck, Alexander Nassen, Bernhard Ugele, et al.
Gene|July 7, 2012
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadiasLars Wittler, Alina Hilger, Judith Proske, et al.
Diagnostics (Basel, Switzerland)|October 25, 2024
Comments and Illustrations of the European Federation of Societies for Ultrasound in Medicine (EFSUMB) Guidelines: Rare Malignant Pulmonal and Pleural Tumors: Primary Pulmonary Sarcoma and Mesothelioma, Imaging Features on Transthoracic UltrasoundKathleen Möller, Florian Dietz, Michael Ludwig, et al.
Frontiers in Bioscience (Landmark Edition)|August 1, 2023
Transforming Growth Factor ß1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic FibrosisJoern Pascal Laubach, Michael Ludwig, Tabea Horn, et al.
International Journal of Molecular Sciences|June 4, 2020
Ubiquitin Carboxyl-Terminal Hydrolases (UCHs): Potential Mediators for Cancer and NeurodegenerationAmit Sharma, Hongde Liu, Fabian Tobar-Tosse, et al.
Pageof 24

Showing results (161-170 of 239) with videos related to

Sort By:
Pageof 24
Molecular Medicine Reports|March 18, 2015
Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouseNirmala Gurung, Greta Grosse, Markus Draaken, et al.
Frontiers in Medicine|December 11, 2023
A blended learning approach for teaching thoracic radiology to medical students: a proof-of-concept studyFabian Stoehr, Yang Yang, Lukas Müller, et al.
International Journal of Molecular Medicine|November 3, 2010
p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissueBonnie J Ching, Lars Wittler, Judith Proske, et al.
Journal of Neurodevelopmental Disorders|April 19, 2016
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVsMadita Schumann, Andrea Hofmann, Sophia K Krutzke, et al.
Birth Defects Research|March 20, 2019
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrumFranziska Kause, Rong Zhang, Michael Ludwig, et al.
Journal of Neurochemistry|April 2, 2004
Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry studyStephan Steckelbroeck, Alexander Nassen, Bernhard Ugele, et al.
Gene|July 7, 2012
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadiasLars Wittler, Alina Hilger, Judith Proske, et al.
Diagnostics (Basel, Switzerland)|October 25, 2024
Comments and Illustrations of the European Federation of Societies for Ultrasound in Medicine (EFSUMB) Guidelines: Rare Malignant Pulmonal and Pleural Tumors: Primary Pulmonary Sarcoma and Mesothelioma, Imaging Features on Transthoracic UltrasoundKathleen Möller, Florian Dietz, Michael Ludwig, et al.
Frontiers in Bioscience (Landmark Edition)|August 1, 2023
Transforming Growth Factor ß1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic FibrosisJoern Pascal Laubach, Michael Ludwig, Tabea Horn, et al.
International Journal of Molecular Sciences|June 4, 2020
Ubiquitin Carboxyl-Terminal Hydrolases (UCHs): Potential Mediators for Cancer and NeurodegenerationAmit Sharma, Hongde Liu, Fabian Tobar-Tosse, et al.
Pageof 24