Gregory Pazour
Affiliations: | Molecular medicine | UMASS Medical School, Worcester, MA, United States |
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"Gregory Pazour"
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Francis RJB, San Agustin JT, Szabo Rogers HL, et al. (2023) Autonomous and non-cell autonomous role of cilia in structural birth defects in mice. Plos Biology. 21: e3002425 |
Francis R, San Agustin JT, Szabo Rogers HL, et al. (2023) Autonomous and non-cell autonomous etiology of ciliopathy associated structural birth defects. Biorxiv : the Preprint Server For Biology |
Bakey Z, Cabrera OA, Hoefele J, et al. (2023) IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Plos Genetics. 19: e1010796 |
Bakey Z, Cabrera OA, Hoefele J, et al. (2023) variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Medrxiv : the Preprint Server For Health Sciences |
Braschi B, Omran H, Witman GB, et al. (2022) Consensus nomenclature for dyneins and associated assembly factors. The Journal of Cell Biology. 221 |
Cyge B, Voronina V, Hoque M, et al. (2021) Loss of the ciliary protein Chibby1 in mice leads to exocrine pancreatic degeneration and pancreatitis. Scientific Reports. 11: 17220 |
Stuck MW, Chong WM, Liao JC, et al. (2021) Rab34 is necessary for early stages of intracellular ciliogenesis. Current Biology : Cb |
Wang Z, Shi Y, Ma S, et al. (2019) Abnormal fertility, acrosome formation, IFT20 expression and localization in the conditional knockout mice. American Journal of Physiology. Cell Physiology |
Shi L, Zhou T, Huang Q, et al. (2019) Intraflagellar transport protein 74 is essential for spermatogenesis and male fertility in mice‡. Biology of Reproduction |
Wehrle A, Witkos TM, Unger S, et al. (2019) Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. Jci Insight. 4 |