Kimberly N Forlenza - JoVE Visualize

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Journal of Infusion Nursing : the Official Publication of the Infusion Nurses Society|September 4, 2020

Standardizing Preoperative Evaluation for Pediatric Central Venous Access: A Care Algorithm to Improve SafetyMonica L Wagner, Darcy Doellman, Kimberly N Forlenza, et al.

Bone Research|April 27, 2022

Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse modelJennifer Zieba, Kimberly N Forlenza, Kelly Heard, et al.

Scientific Reports|September 27, 2016

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly SyndromeIvan Duran, S Paige Taylor, Wenjuan Zhang, et al.

Human Mutation|October 26, 2017

Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathiesWenjuan Zhang, S Paige Taylor, Hayley A Ennis, et al.

Scientific Reports|February 17, 2017

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.

Human Molecular Genetics|July 29, 2016

An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.

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Showing results (1-10 of 6) with videos related to

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Pageof 1

Journal of Infusion Nursing : the Official Publication of the Infusion Nurses Society|September 4, 2020

Standardizing Preoperative Evaluation for Pediatric Central Venous Access: A Care Algorithm to Improve SafetyMonica L Wagner, Darcy Doellman, Kimberly N Forlenza, et al.

Bone Research|April 27, 2022

Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse modelJennifer Zieba, Kimberly N Forlenza, Kelly Heard, et al.

Scientific Reports|September 27, 2016

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly SyndromeIvan Duran, S Paige Taylor, Wenjuan Zhang, et al.

Human Mutation|October 26, 2017

Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathiesWenjuan Zhang, S Paige Taylor, Hayley A Ennis, et al.

Scientific Reports|February 17, 2017

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.

Human Molecular Genetics|July 29, 2016

An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.

Pageof 1