Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ian A Glass

Showing results (41-50 of 113) with videos related to

Pageof 12
Sort By:
Cell Reports. Medicine|June 18, 2025
The human neural cell atlas of Zika virus infection in developing brain tissueCaleb Stokes, Leanne S Whitmore, Dante Moreno, et al.
Cell Reports|May 29, 2026
Retinoic acid regulates foveal development in the human retinaJuliette Wohlschlegel, Lew Kaplan, Lydia R Lee, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRIDan Doherty, Ian A Glass, Joseph R Siebert, et al.
Neurobiology of Disease|April 29, 2006
Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron diseaseYing-Zhang Chen, Sayed H Hashemi, Susan K Anderson, et al.
The Journal of Biological Chemistry|March 28, 2013
The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactionsKarina Tuz, Yi-Chun Hsiao, Oscar Juárez, et al.
American Journal of Human Genetics|May 13, 2004
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndromeMelissa A Parisi, Craig L Bennett, Melissa L Eckert, et al.
American Journal of Medical Genetics. Part A|June 9, 2022
A unique cardiovascular presentation of Marfan syndromeAndrea Otero Luna, Kaylee B Park, Jenna Schauer, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Clinical Interventions and Inflammatory Signaling Shape the Transcriptional and Cellular Architecture of the Early Postnatal LungTristan Frum, Angeline Wu, Marcela S Ymayo, et al.
American Journal of Medical Genetics. Part A|February 26, 2004
Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromesJoseph G Gleeson, Lesley C Keeler, Melissa A Parisi, et al.
Human Genetics|December 14, 2006
A case of true hermaphroditism reveals an unusual mechanism of twinningVivienne L Souter, Melissa A Parisi, Dale R Nyholt, et al.
Pageof 12

Showing results (41-50 of 113) with videos related to

Sort By:
Pageof 12
Cell Reports. Medicine|June 18, 2025
The human neural cell atlas of Zika virus infection in developing brain tissueCaleb Stokes, Leanne S Whitmore, Dante Moreno, et al.
Cell Reports|May 29, 2026
Retinoic acid regulates foveal development in the human retinaJuliette Wohlschlegel, Lew Kaplan, Lydia R Lee, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRIDan Doherty, Ian A Glass, Joseph R Siebert, et al.
Neurobiology of Disease|April 29, 2006
Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron diseaseYing-Zhang Chen, Sayed H Hashemi, Susan K Anderson, et al.
The Journal of Biological Chemistry|March 28, 2013
The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactionsKarina Tuz, Yi-Chun Hsiao, Oscar Juárez, et al.
American Journal of Human Genetics|May 13, 2004
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndromeMelissa A Parisi, Craig L Bennett, Melissa L Eckert, et al.
American Journal of Medical Genetics. Part A|June 9, 2022
A unique cardiovascular presentation of Marfan syndromeAndrea Otero Luna, Kaylee B Park, Jenna Schauer, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Clinical Interventions and Inflammatory Signaling Shape the Transcriptional and Cellular Architecture of the Early Postnatal LungTristan Frum, Angeline Wu, Marcela S Ymayo, et al.
American Journal of Medical Genetics. Part A|February 26, 2004
Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromesJoseph G Gleeson, Lesley C Keeler, Melissa A Parisi, et al.
Human Genetics|December 14, 2006
A case of true hermaphroditism reveals an unusual mechanism of twinningVivienne L Souter, Melissa A Parisi, Dale R Nyholt, et al.
Pageof 12