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Genes
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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 syndrome
Katherina Walz, Juan I Young
Current Genomics
|
June 2, 2011
Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior
Paulina Carmona-Mora, Katherina Walz
EMBO Molecular Medicine
|
January 5, 2011
Copy number variation and susceptibility to complex traits
Cesar P Canales, Katherina Walz
Plos One
|
July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome
Bredford 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 America
Maria 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 dysplasia
Alejo 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 CK2
Alicia 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.
Page
of 6
Search research articles
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Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 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 syndrome
Katherina Walz, Juan I Young
Current Genomics
|
June 2, 2011
Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior
Paulina Carmona-Mora, Katherina Walz
EMBO Molecular Medicine
|
January 5, 2011
Copy number variation and susceptibility to complex traits
Cesar P Canales, Katherina Walz
Plos One
|
July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome
Bredford 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 America
Maria 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 dysplasia
Alejo 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 CK2
Alicia 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.
Page
of 6