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Michael Ludwig

Showing results (201-210 of 239) with videos related to

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Iscience|August 13, 2025
Interferon signaling modulates Down syndrome-associated Alzheimer's disease pathology in a mouse modelPaula Araya, Brian Niemeyer, Kyndal Schade, et al.
Ultrasound International Open|October 15, 2024
Insights Into Modern Undergraduate Ultrasound Education: Prospective Comparison of Digital and Analog Teaching Resources in a Flipped Classroom Concept - The DIvAN StudyJohannes M Weimer, Florian Recker, Leonie Horn, et al.
Cancers|August 27, 2021
PPAR-Responsive Elements Enriched with Alu Repeats May Contribute to Distinctive PPARγ-DNMT1 Interactions in the GenomeAmit Sharma, Fabian Tobar-Tosse, Tikam Chand Dakal, et al.
Cell Reports|November 18, 2020
JAK1 Inhibition Blocks Lethal Immune Hypersensitivity in a Mouse Model of Down SyndromeKathryn D Tuttle, Katherine A Waugh, Paula Araya, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2012
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorderAnna Carina Schulz, Enrika Bartels, Rüdiger Stressig, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Pediatric Surgery International|May 15, 2012
Inheritance of the VATER/VACTERL associationEnrika Bartels, Ekkehart Jenetzky, Benjamin D Solomon, et al.
Science (New York, N.Y.)|January 24, 2009
Analysis of Drosophila segmentation network identifies a JNK pathway factor overexpressed in kidney cancerJiang Liu, Murad Ghanim, Lei Xue, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Pageof 24

Showing results (201-210 of 239) with videos related to

Sort By:
Pageof 24
Iscience|August 13, 2025
Interferon signaling modulates Down syndrome-associated Alzheimer's disease pathology in a mouse modelPaula Araya, Brian Niemeyer, Kyndal Schade, et al.
Ultrasound International Open|October 15, 2024
Insights Into Modern Undergraduate Ultrasound Education: Prospective Comparison of Digital and Analog Teaching Resources in a Flipped Classroom Concept - The DIvAN StudyJohannes M Weimer, Florian Recker, Leonie Horn, et al.
Cancers|August 27, 2021
PPAR-Responsive Elements Enriched with Alu Repeats May Contribute to Distinctive PPARγ-DNMT1 Interactions in the GenomeAmit Sharma, Fabian Tobar-Tosse, Tikam Chand Dakal, et al.
Cell Reports|November 18, 2020
JAK1 Inhibition Blocks Lethal Immune Hypersensitivity in a Mouse Model of Down SyndromeKathryn D Tuttle, Katherine A Waugh, Paula Araya, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2012
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorderAnna Carina Schulz, Enrika Bartels, Rüdiger Stressig, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Pediatric Surgery International|May 15, 2012
Inheritance of the VATER/VACTERL associationEnrika Bartels, Ekkehart Jenetzky, Benjamin D Solomon, et al.
Science (New York, N.Y.)|January 24, 2009
Analysis of Drosophila segmentation network identifies a JNK pathway factor overexpressed in kidney cancerJiang Liu, Murad Ghanim, Lei Xue, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Pageof 24