Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Maimoona A Zariwala"'
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:
Wesley R Lewis, Erik B Malarkey, Douglas Tritschler, Raqual Bower, Raymond C Pasek, Jonathan D Porath, Susan E Birket, Sophie Saunier, Corinne Antignac, Michael R Knowles, Margaret W Leigh, Maimoona A Zariwala, Anil K Challa, Robert A Kesterson, Steven M Rowe, Iain A Drummond, John M Parant, Friedhelm Hildebrandt, Mary E Porter, Bradley K Yoder, Nicolas F Berbari
Publikováno v:
PLoS Genetics, Vol 12, Iss 7, p e1006220 (2016)
Ciliopathies are genetic disorders arising from dysfunction of microtubule-based cellular appendages called cilia. Different cilia types possess distinct stereotypic microtubule doublet arrangements with non-motile or 'primary' cilia having a 9+0 and
Externí odkaz:
https://doaj.org/article/7c98f36db5424abc93f80eefd82caaec
Autor:
Jennifer L Taylor-Cousar, Maimoona A Zariwala, Lauranell H Burch, Rhonda G Pace, Mitchell L Drumm, Hollin Calloway, Haiying Fan, Brent W Weston, Fred A Wright, Michael R Knowles, Gene Modifier Study Group
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4270 (2009)
BackgroundThe pulmonary phenotype in cystic fibrosis (CF) is variable; thus, environmental and genetic factors likely contribute to clinical heterogeneity. We hypothesized that genetically determined ABO histo-blood group antigen (ABH) differences in
Externí odkaz:
https://doaj.org/article/61df60e10ca048179da07334e6973944
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:
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
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