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Liza L Cox

Showing results (1-10 of 13) with videos related to

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BMC Immunology|October 8, 2025
IRF6 C-terminal phosphorylation links inflammation and cell-cell adhesion in oral keratinocytes: implications for oral lichen planusY Andrea Osorio-Osorno, Mónica T Parada-Sanchez, Liza L Cox, et al.
The International Journal of Developmental Biology|July 27, 2002
Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate developmentJoy M Richman, Katherine K Fu, Liza L Cox, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 28, 2013
Microtomographic analysis of lower urinary tract obstructionJoseph R Siebert, Kenneth J Smith, Liza L Cox, et al.
The International Journal of Biochemistry & Cell Biology|December 4, 2003
The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesisTimothy C Cox, Timothy J Sadlon, Quenten P Schwarz, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 2, 2015
In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk lociDarryl L Hadsell, Louise A Hadsell, Walter Olea, et al.
Development (Cambridge, England)|June 12, 2016
A distal 594 bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complexJessica M Rosin, Wenjie Li, Liza L Cox, et al.
Genome Biology|December 23, 2008
A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in developmentAlyson Ashe, Daniel K Morgan, Nadia C Whitelaw, et al.
Genome Research|April 15, 2025
Common <i>cis</i>-regulatory variation modifies the penetrance of pathogenic <i>SHROOM3</i> variants in craniofacial microsomiaHao Zhu, Jiao Zhang, Soumya Rao, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
Nature Genetics|June 5, 2023
Triplication of the interferon receptor locus contributes to hallmarks of Down syndrome in a mouse modelKatherine A Waugh, Ross Minter, Jessica Baxter, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
BMC Immunology|October 8, 2025
IRF6 C-terminal phosphorylation links inflammation and cell-cell adhesion in oral keratinocytes: implications for oral lichen planusY Andrea Osorio-Osorno, Mónica T Parada-Sanchez, Liza L Cox, et al.
The International Journal of Developmental Biology|July 27, 2002
Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate developmentJoy M Richman, Katherine K Fu, Liza L Cox, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 28, 2013
Microtomographic analysis of lower urinary tract obstructionJoseph R Siebert, Kenneth J Smith, Liza L Cox, et al.
The International Journal of Biochemistry & Cell Biology|December 4, 2003
The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesisTimothy C Cox, Timothy J Sadlon, Quenten P Schwarz, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 2, 2015
In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk lociDarryl L Hadsell, Louise A Hadsell, Walter Olea, et al.
Development (Cambridge, England)|June 12, 2016
A distal 594 bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complexJessica M Rosin, Wenjie Li, Liza L Cox, et al.
Genome Biology|December 23, 2008
A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in developmentAlyson Ashe, Daniel K Morgan, Nadia C Whitelaw, et al.
Genome Research|April 15, 2025
Common <i>cis</i>-regulatory variation modifies the penetrance of pathogenic <i>SHROOM3</i> variants in craniofacial microsomiaHao Zhu, Jiao Zhang, Soumya Rao, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
Nature Genetics|June 5, 2023
Triplication of the interferon receptor locus contributes to hallmarks of Down syndrome in a mouse modelKatherine A Waugh, Ross Minter, Jessica Baxter, et al.
Pageof 2