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ArticlesPeer ReviewedFull Text
Clinical and genetic features in autosomal recessive and X-linked Alport syndrome
Author / Creator:Wang, Yanyan ; Sivakumar, Vanessa ; Mohammad, Mardhiah ; Colville, Deb ; Storey, Helen ; Flinter, Frances ; Dagher, Hayat ; Savige, Judy
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2014-03, Vol.29 (3), p.391-396
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ArticlesPeer ReviewedFull Text
Effects of PPARγ ligands on TGF-β1-induced epithelial-mesenchymal transition in alveolar epithelial cells
Author / Creator:Tan, Xiahui ; Dagher, Hayat ; Hutton, Craig A ; Bourke, Jane E
Publisher:BioMed Central Ltd
Journal title:Respiratory research, 2010-02, Vol.11 (1), p.21-21, Article 21
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ArticlesPeer ReviewedFull Text
The collαgen III fibril has a “flexi-rod” structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic roles
Author / Creator:Parkin, J. Des ; San Antonio, James D. ; Persikov, Anton V. ; Dagher, Hayat ; Dalgleish, Raymond ; Jensen, Shane T. ; Jeunemaitre, Xavier ; Savige, Judy
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017, Vol.12 (7), p.e0175582-e0175582
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ArticlesPeer ReviewedFull Text
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome
Author / Creator:Savige, Judy ; Ars, Elisabet ; Cotton, Richard G. H. ; Crockett, David ; Dagher, Hayat ; Deltas, Constantinos ; Ding, Jie ; Flinter, Frances ; Pont-Kingdon, Genevieve ; Smaoui, Nizar ; Torra, Roser ; Storey, Helen
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2014-06, Vol.29 (6), p.971-977
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ArticlesPeer ReviewedFull Text
Mutations in the COL4A4 gene in thin basement membrane disease
Author / Creator:Buzza, Mark ; Dagher, Hayat ; Wang, YanYan ; Wilson, Diane ; Babon, Jeffrey J. ; Cotton, Richard G. ; Savige, Judy
Publisher:New York, NY: Elsevier Inc
Journal title:Kidney international, 2003-02, Vol.63 (2), p.447-453
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ArticlesPeer ReviewedFull Text
The coll[alpha]gen III fibril has a "flexi-rod" structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic roles
Author / Creator:Parkin, J. Des ; San Antonio, James D ; Persikov, Anton V ; Dagher, Hayat ; Dalgleish, Raymond ; Jensen, Shane T ; Jeunemaitre, Xavier ; Savige, Judy
Publisher:Public Library of Science
Journal title:PloS one, 2017-07, Vol.12 (7), p.e0175582
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ArticlesPeer ReviewedFull Text
Thin basement membrane nephropathy
Author / Creator:Savige, Judy ; Rana, Kesha ; Tonna, Stephen ; Buzza, Mark ; Dagher, Hayat ; Wang, Yan Yan
Publisher:New York, NY: Elsevier Inc
Journal title:Kidney international, 2003-10, Vol.64 (4), p.1169-1178
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ArticlesPeer ReviewedFull Text
Transforming Growth Factor-β Enhances Rhinovirus Infection by Diminishing Early Innate Responses
Author / Creator:Thomas, Belinda J. ; Lindsay, Mandy ; Dagher, Hayat ; Freezer, Nicholas J. ; Li, Dongsheng ; Ghildyal, Reena ; Bardin, Philip G.
Publisher:United States
Journal title:American journal of respiratory cell and molecular biology, 2009-09, Vol.41 (3), p.339-347
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ArticlesPeer ReviewedFull Text
Effects of PPAR[gamma] ligands on TGF-[beta]1-induced epithelial-mesenchymal transition in alveolar epithelial cells
Author / Creator:Tan, Xiahui ; Dagher, Hayat ; Hutton, Craig A ; Bourke, Jane E
Publisher:BioMed Central Ltd
Journal title:Respiratory research, 2010-02, Vol.11 (1), p.21
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ArticlesPeer ReviewedFull Text
Transforming Growth Factor-{beta} Enhances Rhinovirus Infection by Diminishing Early Innate Responses
Author / Creator:Thomas, Belinda J ; Lindsay, Mandy ; Dagher, Hayat ; Freezer, Nicholas J ; Li, Dongsheng ; Ghildyal, Reena ; Bardin, Philip G
Publisher:New York: Am Thoracic Soc
Journal title:American journal of respiratory cell and molecular biology, 2009-09, Vol.41 (3), p.339
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ArticlesPeer ReviewedFull Text
Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome
Author / Creator:Dagher, Hayat ; Yan Wang, Yan ; Fassett, Rob ; Savige, Judy
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2002-10, Vol.20 (4), p.321-322
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ArticlesPeer ReviewedFull Text
COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome
Author / Creator:BUZZA, Mark ; YAN YAN WANG ; DAGHER, Hayat ; BABON, Jeffrey J ; COTTON, Richard G ; POWELL, Harley ; DOWLING, John ; SAVIGE, Judy
Publisher:New York, NY: Nature Publishing
Journal title:Kidney international, 2001-08, Vol.60 (2), p.480-483
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ArticlesPeer ReviewedFull Text
Effects of PPAR gamma ligands on TGF-beta1-induced epithelial-mesenchymal transition in alveolar epithelial cells
Author / Creator:Tan, Xiahui ; Dagher, Hayat ; Hutton, Craig A ; Bourke, Jane E
Publisher:England
Journal title:Respiratory research, 2010-02, Vol.11, p.21-21
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ArticlesPeer ReviewedFull Text
Haematuria in asymptomatic individuals
Author / Creator:Savige, Judy ; Buzza, Mark ; Dagher, Hayat
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ, 2001-04, Vol.322 (7292), p.942-943
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ArticlesPeer ReviewedFull Text
Haematuria In Asymptomatic Individuals: It Is Often Caused By Inherited Thinning Of The Glomerular Membrane
Author / Creator:Savige, Judy ; Buzza, Mark ; Dagher, Hayat
Publisher:British Medical Association
Journal title:BMJ (Online), 2001-04, Vol.322 (7292), p.942-943
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ArticlesPeer ReviewedFull Text
COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome1
Author / Creator:Buzza, Mark ; Yan Yan Wang ; Dagher, Hayat ; Babon, Jeffrey J ; Cotton, Richard G ; Powell, Harley ; Dowling, John ; Savige, Judy
Publisher:London: Elsevier Limited
Journal title:Kidney international, 2001-08, Vol.60 (2), p.480
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ArticlesPeer ReviewedFull Text
COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799
Author / Creator:Buzza, Mark ; Wang, Yan Yan ; Dagher, Hayat ; Babon, Jeffrey J. ; Cotton, Richard G. ; Powell, Harley ; Dowling, John ; Savige, Judy
Publisher:Elsevier Inc
Journal title:Kidney international, 2001-08, Vol.60 (2), p.480-483
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ArticlesFull Text
Haematuria in asymptomatic individuals.(Brief Article)
Author / Creator:Savige, Judy ; Buzza, Mark ; Dagher, Hayat
Publisher:BMJ Publishing Group Ltd
Journal title:BMJ. British medical journal (Overseas and retired doctors edition), 2001-04, Vol.322 (7292), p.942-942
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Clinical and genetic features in autosomal recessive and X-linked Alport syndrome

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Effects of PPARγ ligands on TGF-β1-induced epithelial-mesenchymal transition in alveolar epithelial cells

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The collαgen III fibril has a “flexi-rod” structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic roles

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DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome

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Mutations in the COL4A4 gene in thin basement membrane disease

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The coll[alpha]gen III fibril has a "flexi-rod" structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic roles

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Thin basement membrane nephropathy

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Transforming Growth Factor-β Enhances Rhinovirus Infection by Diminishing Early Innate Responses

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Effects of PPAR[gamma] ligands on TGF-[beta]1-induced epithelial-mesenchymal transition in alveolar epithelial cells

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Transforming Growth Factor-{beta} Enhances Rhinovirus Infection by Diminishing Early Innate Responses

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Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome

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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome

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Effects of PPAR gamma ligands on TGF-beta1-induced epithelial-mesenchymal transition in alveolar epithelial cells

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Haematuria in asymptomatic individuals

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Haematuria In Asymptomatic Individuals: It Is Often Caused By Inherited Thinning Of The Glomerular Membrane

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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome1

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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799

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Haematuria in asymptomatic individuals.(Brief Article)

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