Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation. - Wikidata - thesis-toulmin - TriplyDB

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

http://www.wikidata.org/entity/Q34695450

about

Soluble Urokinase Receptors in Focal Segmental Glomerulosclerosis: A Review on the Scientific Point of View FSGS Recurrence in Adults after Renal Transplantation Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice The Impact of Histologic Variants on FSGS Outcomes Initial steroid sensitivity in children with steroid-resistant nephrotic syndrome predicts post-transplant recurrence Graft loss due to recurrent disease in pediatric kidney transplant recipients on a rapid prednisone discontinuation protocol.Recent progress in the pathophysiology and treatment of FSGS recurrence.Genetic testing in nephrotic syndrome--challenges and opportunities.Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients.The podocyte cytoskeleton--key to a functioning glomerulus in health and disease.Educational paper: the podocytopathies.Recurrent focal segmental glomerulosclerosis: a discrete clinical entity.Therapeutic plasma exchange for the treatment of pediatric renal diseases in 2013.NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing.Management of proteinuria in the transplanted patient.Familial FSGS.Recurrent focal segmental glomerulosclerosis after kidney transplantation.MAGI2 Mutations Cause Congenital Nephrotic Syndrome.The amino acid mutations of the podocin in proteinuria: a meta-analysis.Long-Term Outcome of Kidney Transplantation in Recipients with Focal Segmental Glomerulosclerosis.Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.Application of next-generation sequencing technology to diagnosis and treatment of focal segmental glomerulosclerosis.Molecular Mechanisms of Proteinuria in Focal Segmental Glomerulosclerosis.Monogenic Causes of Proteinuria in Children.Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome Proteinuric Kidney Diseases: A Podocyte's Slit Diaphragm and Cytoskeleton Approach

P2860

Q26738374-54AFCFF0-52E7-47F7-BD04-9858B285F31B Q26752840-18B9B7B4-8D14-48A7-89F9-45ACE609BABD Q26799197-77BEB4C8-BE3E-4BA5-A771-3A4ADCFEC110 Q26822256-5CE1C6F9-0BA5-4811-9186-C1B09ABD594B Q27011243-17EB1155-F1BD-4592-AED8-B893FC080D11 Q33660667-61CFD651-1B9C-4390-A86C-FDE072D6D0D5 Q36164800-A99EE29F-F3EA-4E9F-9433-D2776414BA5E Q36572659-ED8DF08C-611E-44A3-B6E0-A61A47777E84 Q36985443-411EACD5-8BF1-45FD-862D-394164973DED Q37039388-5361C54D-3F7B-4DC2-B357-E481EEDFEBCB Q37928188-A913EC14-F856-4412-9192-310D1BE415D4 Q37949258-4AABBA95-224C-4ED5-A804-05761EED1CD0 Q37975102-2BCE2DA0-0FF5-46FA-9FBC-1D6F79A639F1 Q37979793-B18CAFF7-3DA5-41EE-B64B-96F5CCD7BC98 Q38118112-7754C802-2C29-4832-87DC-B532FB479D05 Q38162417-C6C9B51E-53D9-48F2-BA4B-7618BB4CC2DE Q38193693-67C86D2C-EC91-4B57-9A35-48245A36A2FF Q38243597-6BAB9059-EE64-4A2A-B2F8-87E6C4706E04 Q38244354-8A59BEE7-D4C2-43D7-B599-07503022D6FB Q38359297-47182152-16CE-4DD7-892F-A5431955A4E0 Q39118036-97473F2C-6BAA-453F-827A-63CF21A55E00 Q40695800-DA91489A-67F8-4854-8568-F48F75761281 Q46803769-896315DC-537F-4AE2-98CD-2AA77CCDA9E1 Q48108401-8349F502-316D-49B4-8AC2-3F7B29F62A42 Q52561530-91E898C7-7552-41F3-AB28-BB7F0F5174B0 Q52715295-D6E0F34D-D6CE-4C07-BE6A-D3ABFBFB1B2A Q52723397-703E071B-1673-42E3-9592-04F4225783E9 Q54985317-AEFC7BCC-5C30-4E25-8DDB-9814BCEF1CF9 Q57203706-825D91E9-409F-485F-9957-76BF2DD9347C Q57652246-AF083D32-46C2-4DAD-8BFE-166B28A650B0

P2860

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

http://www.wikidata.org/entity/Q34695450

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年学术文章

@wuu

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

name

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@ast

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@en

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@nl

type

label

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@ast

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@en

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@nl

prefLabel

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@ast

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@en

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@nl

P1433

Q34695450-0600D1EB-AEA2-46BE-939C-FDA090D28EE3

P1476

Q34695450-32247028-7DF2-4001-B9B0-3586933D7D62

P2093

Q34695450-1BA388B2-0338-42D0-8E13-36C28F7F442E

Q34695450-20040277-D665-453D-89D3-EA3716B498FF

Q34695450-25EDACE2-E3BF-46BF-973E-E97C2E63FED2

Q34695450-40111EAA-58FD-477C-AA7B-746F917111EE

Q34695450-543F84E9-0004-479A-B879-AE98DD876D2E

Q34695450-54A6C20D-B89A-4066-A04D-5C04715074D7

Q34695450-5E71851E-C4D6-4D2D-A502-7CEEB22BFA4E

Q34695450-6206D2A8-8435-459F-BB26-7F522F4712D9

Q34695450-7F41720E-EBAC-49E4-B03E-AE54F981CE99

Q34695450-858B166C-9C88-4C14-865F-4A2B60A2B576

P2860

Q34695450-065F7F0D-2693-425F-8C88-48C7E5B7685D

Q34695450-145BC132-9D7A-499E-B826-79A43A9BEE82

Q34695450-19E6533C-4905-458F-B196-93FBFABD41F8

Q34695450-1F937E48-2989-4771-9D63-733CA83644A9

Q34695450-261FCE84-1043-4340-B962-A1EF41B271D3

Q34695450-4D440C71-FD16-4F5E-A784-FD09E1D8468C

Q34695450-5A663579-7515-4524-958E-7798167EFB03

Q34695450-62AD34C5-EBFC-4340-84A3-EAAE150A1F33

Q34695450-6A7F54B1-CE16-4A61-B0CE-5EA0D8159DDE

Q34695450-78DE950A-B799-423D-BC8C-38F3905CCC4C

P304

Q34695450-D4FC4343-BEF1-40DA-842A-D41F96556E46

P31

Q34695450-E184A5E4-5991-4FB9-9F17-BF16B24BCF3E

P356

Q34695450-B1AA76FE-C071-43A4-BCD7-46893B3BA115

P433

Q34695450-6287BC8A-3942-4F85-8A3E-6FBEAD3F0FFC

P478

Q34695450-CBC1A4F7-F558-4C8E-8EAA-470A25585C06

P50

Q34695450-B0A7CE4A-9769-495A-AAD4-7214C3C1B0A5

P577

Q34695450-B8BA4B1C-9911-4E60-B439-B0DE2764D311

P698

Q34695450-4A26B8F0-177A-4BE4-9BB5-4DD83D70DFFE

P932

Q34695450-B838E33D-697B-495B-B594-872B9BE06563

P356

P1433

Journal of the American Society of Nephrology

P1476

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

@en

P2093

Andreas Kowarsch

http://www.w3.org/2001/XMLSchema#string

Burkhard Toenshoff

http://www.w3.org/2001/XMLSchema#string

Franz Schäfer

http://www.w3.org/2001/XMLSchema#string

Gerard Cortina

http://www.w3.org/2001/XMLSchema#string

Gil Chernin

http://www.w3.org/2001/XMLSchema#string

Johannes Zschocke

http://www.w3.org/2001/XMLSchema#string

Karl P Pfeiffer

http://www.w3.org/2001/XMLSchema#string

Katrin Hofer

http://www.w3.org/2001/XMLSchema#string

Lothar B Zimmerhackl

http://www.w3.org/2001/XMLSchema#string

Michelle P Winn

http://www.w3.org/2001/XMLSchema#string

P2860

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome.

Broadening the spectrum of diseases related to podocin mutations.

NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms.

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.

Recurrent disease in renal transplants.

Recurrence of nephrotic syndrome/focal segmental glomerulosclerosis following renal transplantation in children.

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population.

P304

579-585

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1681/ASN.2010010029

http://www.w3.org/2001/XMLSchema#string

P433

3

http://www.w3.org/2001/XMLSchema#string

P478

22

http://www.w3.org/2001/XMLSchema#string

P50

P577

2011-02-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

21355056

http://www.w3.org/2001/XMLSchema#string

P932

3060451

http://www.w3.org/2001/XMLSchema#string