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Quoted phrase not found in phrase index: "Abnormal respiratory motile cilium morphology"
Page 1
Axonemal structures reveal mechanoregulatory and disease mechanisms.
Walton T, Gui M, Velkova S, Fassad MR, Hirst RA, Haarman E, O'Callaghan C, Bottier M, Burgoyne T, Mitchison HM, Brown A. Walton T, et al. Nature. 2023 Jun;618(7965):625-633. doi: 10.1038/s41586-023-06140-2. Epub 2023 May 31. Nature. 2023. PMID: 37258679 Free PMC article.
Motile cilia and flagella beat rhythmically on the surface of cells to power the flow of fluid and to enable spermatozoa and unicellular eukaryotes to swim. In humans, defective ciliary motility can lead to male infertility and a congenital disorder called pr …
Motile cilia and flagella beat rhythmically on the surface of cells to power the flow of fluid and to enable spermatozoa and u …
Motile cilia and airway disease.
Legendre M, Zaragosi LE, Mitchison HM. Legendre M, et al. Semin Cell Dev Biol. 2021 Feb;110:19-33. doi: 10.1016/j.semcdb.2020.11.007. Epub 2020 Dec 2. Semin Cell Dev Biol. 2021. PMID: 33279404 Review.
The inherited human motile ciliopathy disorder, primary ciliary dyskinesia (PCD), can arise from mutations in genes affecting various aspects of motile cilia structure and function through deficient production, transport and assembly of cilia motility …
The inherited human motile ciliopathy disorder, primary ciliary dyskinesia (PCD), can arise from mutations in genes affecting various …
Primary ciliary dyskinesia.
Lobo J, Zariwala MA, Noone PG. Lobo J, et al. Semin Respir Crit Care Med. 2015 Apr;36(2):169-79. doi: 10.1055/s-0035-1546748. Epub 2015 Mar 31. Semin Respir Crit Care Med. 2015. PMID: 25826585 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, and biogenesis leading to chronic infections of the respiratory tract, fertility problems, and disorders of organ laterality. ...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, and biogenesis leading to chronic i …
Primary ciliary dyskinesia in adults.
Honoré I, Burgel PR. Honoré I, et al. Rev Mal Respir. 2016 Feb;33(2):165-89. doi: 10.1016/j.rmr.2015.10.743. Epub 2015 Dec 1. Rev Mal Respir. 2016. PMID: 26654126 Review.
INTRODUCTION: Primary ciliary dyskinesia is an autosomal recessive genetic disorder leading to structural and/or functional abnormalities of motor cilia. Impaired mucociliary clearance is responsible for the development of a multi-organ disease, which particularly a …
INTRODUCTION: Primary ciliary dyskinesia is an autosomal recessive genetic disorder leading to structural and/or functional abnormalities …
Ciliogenesis and ciliary abnormalities.
Hagiwara H, Ohwada N, Aoki T, Takata K. Hagiwara H, et al. Med Electron Microsc. 2000;33(3):109-14. doi: 10.1007/s007950000009. Med Electron Microsc. 2000. PMID: 11810467 Review.
Cilia are motile processes extending from the basal bodies, playing important roles in the mucociliary clearance in the respiratory tract and the transport of the ovum from the ovary to the uterus in mammals. ...Swollen cilia and the bulging type of co …
Cilia are motile processes extending from the basal bodies, playing important roles in the mucociliary clearance in the res …
Primary ciliary dyskinesia: diagnosis and standards of care.
Bush A, Cole P, Hariri M, Mackay I, Phillips G, O'Callaghan C, Wilson R, Warner JO. Bush A, et al. Eur Respir J. 1998 Oct;12(4):982-8. doi: 10.1183/09031936.98.12040982. Eur Respir J. 1998. PMID: 9817179 Free article. Review.
Primary ciliary dyskinesia (PCD) is characterized by disease of the upper and lower respiratory tract, in association with visceral mirror image arrangement in 50% of cases, due to abnormal structure and/or function of cilia. ...Diagnosis is by a cascade of i …
Primary ciliary dyskinesia (PCD) is characterized by disease of the upper and lower respiratory tract, in association with visceral m …
Clinical and molecular features of Joubert syndrome and related disorders.
Parisi MA. Parisi MA. Am J Med Genet C Semin Med Genet. 2009 Nov 15;151C(4):326-40. doi: 10.1002/ajmg.c.30229. Am J Med Genet C Semin Med Genet. 2009. PMID: 19876931 Free PMC article. Review.
Joubert syndrome (JBTS; OMIM 213300) is a rare, autosomal recessive disorder characterized by a specific congenital malformation of the hindbrain and a broad spectrum of other phenotypic findings that is now known to be caused by defects in the structure and/or function of …
Joubert syndrome (JBTS; OMIM 213300) is a rare, autosomal recessive disorder characterized by a specific congenital malformation of t …
Picking up speed: advances in the genetics of primary ciliary dyskinesia.
Horani A, Brody SL, Ferkol TW. Horani A, et al. Pediatr Res. 2014 Jan;75(1-2):158-64. doi: 10.1038/pr.2013.200. Epub 2013 Nov 5. Pediatr Res. 2014. PMID: 24192704 Free PMC article. Review.
While progress in genetics and biology has uncovered numerous cilia-related syndromes, primary ciliary dyskinesia (PCD) remains the sole genetic disorder of motile cilia dysfunction. ...In this article, we will describe the structure, function, and emerging g …
While progress in genetics and biology has uncovered numerous cilia-related syndromes, primary ciliary dyskinesia (PCD) remains the s …
Toward an Earlier Diagnosis of Primary Ciliary Dyskinesia. Which Patients Should Undergo Detailed Diagnostic Testing?
Kuehni CE, Lucas JS. Kuehni CE, et al. Ann Am Thorac Soc. 2016 Aug;13(8):1239-43. doi: 10.1513/AnnalsATS.201605-331PS. Ann Am Thorac Soc. 2016. PMID: 27258773 Free article. Review.
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cilia, leading to chronic upper and lower respiratory symptoms. ...The sensitivity and specificity of the tools are reasonable, but positive and negative predi …
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cilia, leading to chronic upp …
Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.
Bush A, Hogg C. Bush A, et al. Expert Rev Respir Med. 2012 Dec;6(6):663-82. doi: 10.1586/ers.12.60. Expert Rev Respir Med. 2012. PMID: 23234452 Review.
Human cilia were once thought merely to be important in respiratory mucociliary clearance, with primary ciliary dyskinesia (PCD) the sole manifestation of ciliary dysfunction. There are now known to be three types of cilia: primary, nodal and motile. …
Human cilia were once thought merely to be important in respiratory mucociliary clearance, with primary ciliary dyskinesia (PC …
49 results