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
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