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Robert S Krauss

ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 14

Top Venues

eLife

Development (Cambridge, England)

Human mutation

The Journal of physiology

Icahn School of Medicine at Mount Sinai

University of North Carolina at Chapel Hill (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Icahn School of Medicine at Mount Sinai

United States

Professor :: Cell, Developmental, and Regenerative Biology

Education History

University of North Carolina at Chapel Hill

United States

PHD

Publications

Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Erik Jacques, Yinni Kuang, Allison P Kann, Fabien Le Grand, Robert S Krauss, Penney M Gilbert
The mini-IDLE 3D biomimetic culture assay enables interrogation of mechanisms governing muscle stem cell quiescence and niche repopulation. eLife 11 (2022)
Hsiao-Fan Lo, Mingi Hong, Henrietta Szutorisz, Yasmin L Hurd, Robert S Krauss
Δ9-Tetrahydrocannabinol inhibits Hedgehog-dependent patterning during development. Development (Cambridge, England) 148 (19) (2021)
Ju-Hyeon Bae, Mingi Hong, Hyeon-Ju Jeong, Hyebeen Kim, Sang-Jin Lee, Dongryeol Ryu, Gyu-Un Bae, Sung Chun Cho, Young-Sam Lee, Robert S Krauss, Jong-Sun Kang
Satellite cell-specific ablation of Cdon impairs integrin activation, FGF signalling, and muscle regeneration. Journal of cachexia, sarcopenia and muscle 11 (4) (2020)
Mingi Hong, Annabel Christ, Anna Christa, Thomas E Willnow, Robert S Krauss
Cdon mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly. eLife 9 (2020)
Lisbeth Liliendal Valbjørn Møller, Merna Jaurji, Rasmus Kjøbsted, Giselle A Joseph, Agnete B Madsen, Jonas Roland Knudsen, Anne-Marie Lundsgaard, Nicoline R Andersen, Peter Schjerling, Thomas Elbenhardt Jensen, Robert S Krauss, Erik Arne Richter, Lykke Sylow
Insulin-stimulated glucose uptake partly relies on p21-activated kinase (PAK)2, but not PAK1, in mouse skeletal muscle. The Journal of physiology 598 (23) (2020)
Allison P Kann, Robert S Krauss
Multiplexed RNAscope and immunofluorescence on whole-mount skeletal myofibers and their associated stem cells. Development (Cambridge, England) 146 (20) (2019)
Giselle A Joseph, Margaret Hung, Aviva J Goel, Mingi Hong, Marysia-Kolbe Rieder, Noam D Beckmann, Madhavika N Serasinghe, Jerry E Chipuk, Parvathi M Devarakonda, David J Goldhamer, Paulina Aldana-Hernandez, Jonathan Curtis, René L Jacobs, Robert S Krauss
Late-onset megaconial myopathy in mice lacking group I Paks. Skeletal muscle 9 (1) (2019)
Mingi Hong, Robert S Krauss
Modeling the complex etiology of holoprosencephaly in mice. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)
Mingi Hong, Kshitij Srivastava, Sungjin Kim, Benjamin L Allen, Daniel J Leahy, Ping Hu, Erich Roessler, Robert S Krauss, Maximilian Muenke
BOC is a modifier gene in holoprosencephaly. Human mutation 38 (11) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Robert S Krauss