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

Katherina Walz

Showing results (1-10 of 60) with videos related to

Pageof 6
Sort By:
Genes|November 27, 2024
Reply to Elgoyhen et al. Comment on "De Rosa et al. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America. <i>Genes</i> 2024, <i>15</i>, 178"Katherina Walz
Rare Diseases (Austin, Tex.)|March 5, 2016
The methyl binding domain containing protein MBD5 is a transcriptional regulator responsible for 2q23.1 deletion syndromeKatherina Walz, Juan I Young
Current Genomics|June 2, 2011
Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic BehaviorPaulina Carmona-Mora, Katherina Walz
EMBO Molecular Medicine|January 5, 2011
Copy number variation and susceptibility to complex traitsCesar P Canales, Katherina Walz
Plos One|July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndromeBredford Kerr, Pamela A Silva, Katherina Walz, et al.
The Journal of Clinical Investigation|October 7, 2006
Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)Katherina Walz, Richard Paylor, Jiong Yan, et al.
Genes|February 24, 2024
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin AmericaMaria Agustina De Rosa, Maria T Bernardi, Soledad Kleppe, et al.
Communications Biology|November 26, 2025
Glucocorticoid treatment rescues early lethality in a mouse model of geleophysic dysplasiaAlejo Antonio Morales, Vladimir Camarena, Katherina Walz, et al.
Yeast (Chichester, England)|May 2, 2003
cDNA cloning, biochemical and phylogenetic characterization of beta- and beta'-subunits of Candida albicans protein kinase CK2Alicia Zelada, Flávio S J De Souza, Katherina Walz, et al.
Human Molecular Genetics|January 8, 2004
Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2)Katherina Walz, Corinne Spencer, Krista Kaasik, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Genes|November 27, 2024
Reply to Elgoyhen et al. Comment on "De Rosa et al. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America. <i>Genes</i> 2024, <i>15</i>, 178"Katherina Walz
Rare Diseases (Austin, Tex.)|March 5, 2016
The methyl binding domain containing protein MBD5 is a transcriptional regulator responsible for 2q23.1 deletion syndromeKatherina Walz, Juan I Young
Current Genomics|June 2, 2011
Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic BehaviorPaulina Carmona-Mora, Katherina Walz
EMBO Molecular Medicine|January 5, 2011
Copy number variation and susceptibility to complex traitsCesar P Canales, Katherina Walz
Plos One|July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndromeBredford Kerr, Pamela A Silva, Katherina Walz, et al.
The Journal of Clinical Investigation|October 7, 2006
Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)Katherina Walz, Richard Paylor, Jiong Yan, et al.
Genes|February 24, 2024
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin AmericaMaria Agustina De Rosa, Maria T Bernardi, Soledad Kleppe, et al.
Communications Biology|November 26, 2025
Glucocorticoid treatment rescues early lethality in a mouse model of geleophysic dysplasiaAlejo Antonio Morales, Vladimir Camarena, Katherina Walz, et al.
Yeast (Chichester, England)|May 2, 2003
cDNA cloning, biochemical and phylogenetic characterization of beta- and beta'-subunits of Candida albicans protein kinase CK2Alicia Zelada, Flávio S J De Souza, Katherina Walz, et al.
Human Molecular Genetics|January 8, 2004
Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2)Katherina Walz, Corinne Spencer, Krista Kaasik, et al.
Pageof 6