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Molecular circumscription and major evolutionary lineages of the fern genus Dryopteris (Dryopteridaceae)

BMC evolutionary biology, 2012-09, Vol.12 (1), p.180

2012

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Unraveling reticulate evolution in North American Dryopteris (Dryopteridaceae)

BMC evolutionary biology, 2012-06, Vol.12 (1), p.104

2012

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Reticulate evolution on a global scale: A nuclear phylogeny for New World Dryopteris (Dryopteridaceae)

Molecular phylogenetics and evolution, 2012-09, Vol.64 (3), p.563-581

2012

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An Exploration into Fern Genome Space

Genome biology and evolution, 2015-09, Vol.7 (9), p.2533-2544

2015

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Employing hypothesis testing and data from multiple genomic compartments to resolve recalcitrant backbone nodes in Goodenia s.l. (Goodeniaceae)

Molecular phylogenetics and evolution, 2018-10, Vol.127, p.502-512

2018

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Utilizing next-generation sequencing to resolve the backbone of the Core Goodeniaceae and inform future taxonomic and floral form studies

Molecular phylogenetics and evolution, 2016-01, Vol.94 (Pt B), p.605-617

2016

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Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes

American journal of human genetics, 2021-04, Vol.108 (4), p.722-738

2021

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In Vivo Modulation of Nogo-B Attenuates Neointima Formation

Molecular therapy, 2008-11, Vol.16 (11), p.1798-1804

2008

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Engineered zinc-finger proteins can compensate genetic haploinsufficiency by transcriptional activation of the wild-type allele: application to Willams-Beuren syndrome and supravalvular aortic stenosis

Human gene therapy, 2012-11, Vol.23 (11), p.1186-1199

2012

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Complex Loci in human and mouse genomes

PLoS genetics, 2006-04, Vol.2 (4), p.e47-e47

2006

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Renal pathological changes in Fabry disease

Journal of inherited metabolic disease, 2001-01, Vol.24 (S2), p.66-70

2001

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Renal Manifestations of Tuberous Sclerosis Complex

Contributions to nephrology, 1997-01, Vol.122, p.64-75

1997

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Physical map of the D6S149-D6S193 region on chromosome 6Q27 and its involvement in benign surface epithelial ovarian tumours

Oncogene, 1998-03, Vol.16 (12), p.1639-1642

1998

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Molecular Genetic Investigations in Autosomal Dominant Polycystic Kidney Disease. Gene Mutation Detection, Linkage Analysis, and Preliminary ACE Gene I/D Polymorphism Association Studies: An Update

Contributions to nephrology, 1997-01, Vol.122, p.53-57

1997

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Vessel malformation in a patient with ADPKD: megadolichobasilar artery, abdominal aortic and iliac aneurysms

Contributions to nephrology, 1995, Vol.115, p.182

1995

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Nephronophthisis-Medullary Cystic Kidney Disease Complex: A Report on 24 Patients from 5 Families with Italian Ancestry

Contributions to nephrology, 1997-01, Vol.122, p.61-63

1997

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A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney disease

Contributions to nephrology, 1997, Vol.122, p.91-95

1997

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An Information Center for Rare Diseases: A Tool for Epidemiologic and Clinical Studies in Rare Diseases

Contributions to nephrology, 1997-01, Vol.122, p.207-210

1997

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The Kidney and Von Hippel-Lindau Disease: Impact of Molecular Genetic Analysis of the VHL Gene for Clinical Management

Contributions to nephrology, 1997-01, Vol.122, p.102-108

1997

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Genetic Approach to the Study of Cellular Ion Transport Anomalies in Idiopathic Calcium Nephrolithiasis

Contributions to nephrology, 1997-01, Vol.122, p.189-192

1997

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Oral-Facial-Digital Syndrome Type 1 Coexisting with Polycystic Kidney Disease

Contributions to nephrology, 1997-01, Vol.122, p.58-60

1997

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Planning Kidney Surgery in Von Hippel-Lindau Disease

Contributions to nephrology, 1997-01, Vol.122, p.112-115

1997

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Prevalence of Hypertension According to Phenotype and Gender in Autosomal-Dominant Polycystic Kidney Disease

Contributions to nephrology, 1997-01, Vol.122, p.17-21

1997

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Kidney transplantation in Alport's syndrome

Contributions to nephrology, 1997, Vol.122, p.140-142

1997

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Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes

Contributions to nephrology, 1995, Vol.115, p.88

1995

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Molecular circumscription and major evolutionary lineages of the fern genus Dryopteris (Dryopteridaceae)

Unraveling reticulate evolution in North American Dryopteris (Dryopteridaceae)

Reticulate evolution on a global scale: A nuclear phylogeny for New World Dryopteris (Dryopteridaceae)

An Exploration into Fern Genome Space

Employing hypothesis testing and data from multiple genomic compartments to resolve recalcitrant backbone nodes in Goodenia s.l. (Goodeniaceae)

Utilizing next-generation sequencing to resolve the backbone of the Core Goodeniaceae and inform future taxonomic and floral form studies

Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes

In Vivo Modulation of Nogo-B Attenuates Neointima Formation

Engineered zinc-finger proteins can compensate genetic haploinsufficiency by transcriptional activation of the wild-type allele: application to Willams-Beuren syndrome and supravalvular aortic stenosis

Complex Loci in human and mouse genomes

Renal pathological changes in Fabry disease

Renal Manifestations of Tuberous Sclerosis Complex

Physical map of the D6S149-D6S193 region on chromosome 6Q27 and its involvement in benign surface epithelial ovarian tumours

Molecular Genetic Investigations in Autosomal Dominant Polycystic Kidney Disease. Gene Mutation Detection, Linkage Analysis, and Preliminary ACE Gene I/D Polymorphism Association Studies: An Update

Vessel malformation in a patient with ADPKD: megadolichobasilar artery, abdominal aortic and iliac aneurysms

Nephronophthisis-Medullary Cystic Kidney Disease Complex: A Report on 24 Patients from 5 Families with Italian Ancestry

A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney disease

An Information Center for Rare Diseases: A Tool for Epidemiologic and Clinical Studies in Rare Diseases

The Kidney and Von Hippel-Lindau Disease: Impact of Molecular Genetic Analysis of the VHL Gene for Clinical Management

Genetic Approach to the Study of Cellular Ion Transport Anomalies in Idiopathic Calcium Nephrolithiasis

Oral-Facial-Digital Syndrome Type 1 Coexisting with Polycystic Kidney Disease

Planning Kidney Surgery in Von Hippel-Lindau Disease

Prevalence of Hypertension According to Phenotype and Gender in Autosomal-Dominant Polycystic Kidney Disease

Kidney transplantation in Alport's syndrome

Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes

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