(Q81692071)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

review article

1 reference

title

Familial hematurias: what we know and what we don't (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

author name string

Clifford E Kashtan

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

publication date

27 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

page(s)

1027-1035

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15856317%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00467-005-1859-z

11 January 2020

exact match

0 references

cites work

Enalapril in paediatric patients with Alport syndrome: 2 years' experience

1 reference

12 December 2020

A novel surgical organ perfusion method for effective ex vivo and in vivo gene transfer into renal glomerular cells

1 reference

12 December 2020

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

1 reference

12 December 2020

Adenovirus-mediated gene transfer into kidney glomeruli using an ex vivo and in vivo kidney perfusion system - first steps towards gene therapy of Alport syndrome.

1 reference

12 December 2020

Long-term effects of cyclosporine A in Alport's syndrome

1 reference

12 December 2020

Incidence of thin membrane nephropathy: morphometric investigation of a population sample

1 reference

12 December 2020

Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome

1 reference

12 December 2020

Abnormal glomerular basement membrane laminins in murine, canine, and human Alport syndrome: aberrant laminin alpha2 deposition is species independent

1 reference

12 December 2020

Glomerular endothelial cells and podocytes jointly synthesize laminin-1 and -11 chains

1 reference

12 December 2020

Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution

1 reference

12 December 2020

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome

1 reference

12 December 2020

Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis

1 reference

12 December 2020

Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome

1 reference

12 December 2020

Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody

1 reference

12 December 2020

Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene

1 reference

12 December 2020

Red cell traverse through thin glomerular basement membrane

1 reference

12 December 2020

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

1 reference

12 December 2020

Temporal bone histopathology in alport syndrome.

1 reference

12 December 2020

Contemporary diagnostic approach in Alport's syndrome

1 reference

12 December 2020

Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor

1 reference

12 December 2020

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene

1 reference

12 December 2020

Enalapril in children with Alport syndrome

1 reference

12 December 2020

Immunohistologic studies of type IV collagen in anterior lens capsules of patients with Alport syndrome

1 reference

12 December 2020

Role for transforming growth factor-beta1 in alport renal disease progression.

1 reference

12 December 2020

Effect of cyclosporin A on proteinuria in patients with Alport's syndrome

1 reference

12 December 2020

Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis

1 reference

12 December 2020

In hereditary nephritis angiotensin-converting enzyme inhibition decreases proteinuria and may slow the rate of progression

1 reference

12 December 2020

New form of X-linked dominant hereditary nephritis in dogs

1 reference

12 December 2020

Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure

1 reference

12 December 2020

The clinical spectrum of type IV collagen mutations

1 reference

12 December 2020

Chronology of renal scarring in males with Alport syndrome

1 reference

12 December 2020

Ocular manifestations of autosomal recessive Alport syndrome

1 reference

12 December 2020

Expression of basement membrane type IV collagen chains during postnatal development in the murine cochlea.

1 reference

12 December 2020

Renal prognosis in women with hereditary nephritis.

1 reference

12 December 2020

Increased expression of MMP-2, MMP-9 (type IV collagenases/gelatinases), and MT1-MMP in canine X-linked Alport syndrome (XLAS).

1 reference

12 December 2020

Integrin alpha1beta1 and transforming growth factor-beta1 play distinct roles in alport glomerular pathogenesis and serve as dual targets for metabolic therapy

1 reference

12 December 2020

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

1 reference

12 December 2020

Mutations in the COL4A4 gene in thin basement membrane disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Laminin-1 reexpression in Alport mouse glomerular basement membranes

1 reference

12 December 2020

Transfer of the alpha 5(IV) collagen chain gene to smooth muscle restores in vivo expression of the alpha 6(IV) collagen chain in a canine model of Alport syndrome

1 reference

12 December 2020

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV

1 reference

12 December 2020

Alport's syndrome. A report of 58 cases and a review of the literature

1 reference

12 December 2020

Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical region

1 reference

12 December 2020

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome

1 reference

12 December 2020

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

1 reference

12 December 2020

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome

1 reference

12 December 2020

Autosomal recessive Alport syndrome: mutation in the COL4A3 gene in a woman with Alport syndrome and posttransplant antiglomerular basement membrane nephritis

1 reference

12 December 2020

Role of distinct type IV collagen networks in glomerular development and function

1 reference

12 December 2020

Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours

1 reference

12 December 2020

Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome

1 reference

12 December 2020

Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.

1 reference

12 December 2020

Antifibrotic, nephroprotective potential of ACE inhibitor vs AT1 antagonist in a murine model of renal fibrosis

1 reference

12 December 2020

Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients

1 reference

12 December 2020

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes

1 reference

12 December 2020

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

1 reference

12 December 2020

Can Alport syndrome be treated by gene therapy?

1 reference

12 December 2020

Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.

1 reference

12 December 2020

Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model

1 reference

12 December 2020

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome

1 reference

12 December 2020

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

1 reference

12 December 2020

LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis

1 reference

12 December 2020

The molecular basis of Goodpasture and Alport syndromes: beacons for the discovery of the collagen IV family

1 reference

12 December 2020

Lens capsule abnormalities in Alport's syndrome

1 reference

12 December 2020

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

1 reference

12 December 2020

Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome

1 reference

12 December 2020

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

12 December 2020

Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease-The Limburg Renal Registry

1 reference

12 December 2020

A model of autosomal recessive Alport syndrome in English cocker spaniel dogs

1 reference

12 December 2020

Bone morphogenic protein-7 inhibits progression of chronic renal fibrosis associated with two genetic mouse models

1 reference

12 December 2020

Recurrent corneal erosion associated with Alport's syndrome. Rapid communication

1 reference

12 December 2020

Angiotensin converting enzyme inhibitor therapy in children with Alport syndrome: effect on urinary albumin, TGF-beta, and nitrite excretion

1 reference

12 December 2020

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

12 December 2020

Ultrastructural appearance of renal and other basement membranes in the Bull terrier model of autosomal dominant hereditary nephritis.

1 reference

12 December 2020

1 reference

12 December 2020

Alport syndrome. A review of the ocular manifestations

1 reference

12 December 2020

1 reference

12 December 2020