Zobrazeno 1 - 10
of 179
pro vyhledávání: '"Maimoona A Zariwala"'
Publikováno v:
Cells, Vol 13, Iss 11, p 974 (2024)
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, motile ciliopathy, characterized by neonatal respiratory distress, recurrent upper and lower respiratory tract infections, subfertility, and laterality defects. Diagnosis relies o
Externí odkaz:
https://doaj.org/article/bc5236c1dd8744cfb2385882a9fed055
Autor:
Adam J. Shapiro, Kimberley Kaspy, M. Leigh Ann Daniels, Jaclyn R. Stonebraker, Van‐Hung Nguyen, Lyne Joyal, Michael R. Knowles, Maimoona A. Zariwala
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Background Primary ciliary dyskinesia (PCD) is a mostly autosomal recessive, genetic disease of abnormal motile cilia function, resulting in bronchiectasis, infertility, organ laterality defects, and chronic otolaryngology disease. Though mo
Externí odkaz:
https://doaj.org/article/88d3f62e6430487ba83e8d3d4331ea81
Autor:
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, Frankline Onchiri, Thomas W. Ferkol, Scott D. Sagel, Sharon D. Dell, Carlos Milla, Adam J. Shapiro, Kelli M. Sullivan, Maimoona A. Zariwala, Jessica E. Pittman, Federico Mollica, Harm A. W. M. Tiddens, Mariette Kemner-van de Corput, Michael R. Knowles, Stephanie D. Davis, Margaret W. Leigh
Publikováno v:
Annals of the American Thoracic Society. 20:539-547
Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance, recurrent respiratory infections, and progressive airway damage and obstructive lung disease. While the association of ciliary ultrastructure defect/genotype with se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d68c1905d6dec4efdcb1c5618c9514f
https://doi.org/10.1513/annalsats.202206-524oc
https://doi.org/10.1513/annalsats.202206-524oc
Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype
Autor:
Andrew T. Barber, Adam J. Shapiro, Stephanie D. Davis, Thomas W. Ferkol, Jeffrey J. Atkinson, Scott D. Sagel, Sharon D. Dell, Kenneth N. Olivier, Carlos E. Milla, Margaret Rosenfeld, Lang Li, Feng-Chang Lin, Kelli M. Sullivan, Nicole A. Capps, Maimoona A. Zariwala, Michael R. Knowles, Margaret W. Leigh
Publikováno v:
Annals of the American Thoracic Society. 20:397-405
The association between organ laterality abnormalities and ciliary ultrastructural defect or genotype in primary ciliary dyskinesia is poorly understood.To determine if there is an association between presence/type of laterality abnormality and cilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98b324634872e405094b9acc2bedfe0
https://doi.org/10.1513/annalsats.202206-487oc
https://doi.org/10.1513/annalsats.202206-487oc
Autor:
Wallace B. Wee, Margaret W. Leigh, Stephanie D. Davis, Margaret Rosenfeld, Kelli M. Sullivan, Michael G. Sawras, Thomas W. Ferkol, Michael R. Knowles, Carlos Milla, Scott D. Sagel, Maimoona A. Zariwala, Eleanor Pullenayegum, Sharon D. Dell
Publikováno v:
Annals of the American Thoracic Society. 19(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f92119d9714c5db7d03ef57582d197fb
https://pubmed.ncbi.nlm.nih.gov/35657736
https://pubmed.ncbi.nlm.nih.gov/35657736
Publikováno v:
American journal of respiratory cell and molecular biology. 67(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b38cdced2a8c2a53a2a4abd03e239be9
https://pubmed.ncbi.nlm.nih.gov/36178856
https://pubmed.ncbi.nlm.nih.gov/36178856
Autor:
Adam J. Shapiro, Guillaume Sillon, Daniela D’Agostino, Laurence Baret, Francesc López-Giráldez, Shrikant Mane, Margaret W. Leigh, Stephanie D. Davis, Michael R. Knowles, Maimoona A. Zariwala
Publikováno v:
Annals of the American Thoracic Society. 20:140-144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c1cb9b10902fce67f33d0fb2e9968e1
https://doi.org/10.1513/annalsats.202203-253rl
https://doi.org/10.1513/annalsats.202203-253rl
Autor:
Ximena M Bustamante-Marin, Amjad Horani, Mihaela Stoyanova, Wu-Lin Charng, Mathieu Bottier, Patrick R Sears, Wei-Ning Yin, Leigh Anne Daniels, Hailey Bowen, Donald F Conrad, Michael R Knowles, Lawrence E Ostrowski, Maimoona A Zariwala, Susan K Dutcher
Publikováno v:
PLoS Genetics, Vol 16, Iss 8, p e1008691 (2020)
Primary ciliary dyskinesia (PCD) is characterized by chronic airway disease, reduced fertility, and randomization of the left/right body axis. It is caused by defects of motile cilia and sperm flagella. We screened a cohort of affected individuals th
Externí odkaz:
https://doaj.org/article/ed560ccc4d4b41219172bc6473260ff5
Autor:
Lawrence E. Ostrowski, Weining Yin, Amanda J. Smith, Patrick R. Sears, Ximena M. Bustamante-Marin, Hong Dang, Friedhelm Hildebrandt, Leigh Anne Daniels, Nicole A. Capps, Kelli M. Sullivan, Margaret W. Leigh, Maimoona A. Zariwala, Michael R. Knowles
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1753 (2022)
Primary ciliary dyskinesia (PCD) is a rare lung disease caused by mutations that impair the function of motile cilia, resulting in chronic upper and lower respiratory disease, reduced fertility, and a high prevalence of situs abnormalities. The disea
Externí odkaz:
https://doaj.org/article/4b3988c221d24482b992cdf7a4bd437e
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 67:511-514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bf465c3440e63d0973fdb3ad74805a0
https://doi.org/10.1165/rcmb.2022-0176le
https://doi.org/10.1165/rcmb.2022-0176le