Literature DB >> 19282856

Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.

Friedhelm Hildebrandt1, Saskia F Heeringa.   

Abstract

In steroid-resistant nephrotic syndrome (SRNS) Machuca et al. report that mutations of the recessive podocin gene cause adult-onset SRNS if the R229Q genetic variant occurs in a compound heterozygous state with another podocin mutation. Learning to tell apart the specific allele combinations of podocin mutations will be important for prognosis, genetic counseling in living related kidney donation, accurate etiologic classification within treatment studies, and the understanding of podocin function.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19282856     DOI: 10.1038/ki.2008.693

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  23 in total

1.  Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.

Authors:  Eduardo Machuca; Geneviève Benoit; Fabien Nevo; Marie-Josèphe Tête; Olivier Gribouval; Audrey Pawtowski; Per Brandström; Chantal Loirat; Patrick Niaudet; Marie-Claire Gubler; Corinne Antignac
Journal:  J Am Soc Nephrol       Date:  2010-05-27       Impact factor: 10.121

2.  Protective effects of low-dose rapamycin combined with valsartan on podocytes of diabetic rats.

Authors:  Jin Zhang; Xiaozhou Hu; Shaoting Wang; Yan Zhang; Hong Yang
Journal:  Int J Clin Exp Med       Date:  2015-08-15

3.  Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

Authors:  Daniela A Braun; Jia Rao; Geraldine Mollet; David Schapiro; Marie-Claire Daugeron; Weizhen Tan; Olivier Gribouval; Olivia Boyer; Patrick Revy; Tilman Jobst-Schwan; Johanna Magdalena Schmidt; Jennifer A Lawson; Denny Schanze; Shazia Ashraf; Jeremy F P Ullmann; Charlotte A Hoogstraten; Nathalie Boddaert; Bruno Collinet; Gaëlle Martin; Dominique Liger; Svjetlana Lovric; Monica Furlano; I Chiara Guerrera; Oraly Sanchez-Ferras; Jennifer F Hu; Anne-Claire Boschat; Sylvia Sanquer; Björn Menten; Sarah Vergult; Nina De Rocker; Merlin Airik; Tobias Hermle; Shirlee Shril; Eugen Widmeier; Heon Yung Gee; Won-Il Choi; Carolin E Sadowski; Werner L Pabst; Jillian K Warejko; Ankana Daga; Tamara Basta; Verena Matejas; Karin Scharmann; Sandra D Kienast; Babak Behnam; Brendan Beeson; Amber Begtrup; Malcolm Bruce; Gaik-Siew Ch'ng; Shuan-Pei Lin; Jui-Hsing Chang; Chao-Huei Chen; Megan T Cho; Patrick M Gaffney; Patrick E Gipson; Chyong-Hsin Hsu; Jameela A Kari; Yu-Yuan Ke; Cathy Kiraly-Borri; Wai-Ming Lai; Emmanuelle Lemyre; Rebecca Okashah Littlejohn; Amira Masri; Mastaneh Moghtaderi; Kazuyuki Nakamura; Fatih Ozaltin; Marleen Praet; Chitra Prasad; Agnieszka Prytula; Elizabeth R Roeder; Patrick Rump; Rhonda E Schnur; Takashi Shiihara; Manish D Sinha; Neveen A Soliman; Kenza Soulami; David A Sweetser; Wen-Hui Tsai; Jeng-Daw Tsai; Rezan Topaloglu; Udo Vester; David H Viskochil; Nithiwat Vatanavicharn; Jessica L Waxler; Klaas J Wierenga; Matthias T F Wolf; Sik-Nin Wong; Sebastian A Leidel; Gessica Truglio; Peter C Dedon; Annapurna Poduri; Shrikant Mane; Richard P Lifton; Maxime Bouchard; Peter Kannu; David Chitayat; Daniella Magen; Bert Callewaert; Herman van Tilbeurgh; Martin Zenker; Corinne Antignac; Friedhelm Hildebrandt
Journal:  Nat Genet       Date:  2017-08-14       Impact factor: 38.330

4.  Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.

Authors:  Svjetlana Lovric; Humphrey Fang; Virginia Vega-Warner; Carolin E Sadowski; Heon Yung Gee; Jan Halbritter; Shazia Ashraf; Pawaree Saisawat; Neveen A Soliman; Jameela A Kari; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Clin J Am Soc Nephrol       Date:  2014-04-17       Impact factor: 8.237

5.  Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency.

Authors:  Svjetlana Lovric; Sara Goncalves; Heon Yung Gee; Babak Oskouian; Honnappa Srinivas; Won-Il Choi; Shirlee Shril; Shazia Ashraf; Weizhen Tan; Jia Rao; Merlin Airik; David Schapiro; Daniela A Braun; Carolin E Sadowski; Eugen Widmeier; Tilman Jobst-Schwan; Johanna Magdalena Schmidt; Vladimir Girik; Guido Capitani; Jung H Suh; Noëlle Lachaussée; Christelle Arrondel; Julie Patat; Olivier Gribouval; Monica Furlano; Olivia Boyer; Alain Schmitt; Vincent Vuiblet; Seema Hashmi; Rainer Wilcken; Francois P Bernier; A Micheil Innes; Jillian S Parboosingh; Ryan E Lamont; Julian P Midgley; Nicola Wright; Jacek Majewski; Martin Zenker; Franz Schaefer; Navina Kuss; Johann Greil; Thomas Giese; Klaus Schwarz; Vilain Catheline; Denny Schanze; Ingolf Franke; Yves Sznajer; Anne S Truant; Brigitte Adams; Julie Désir; Ronald Biemann; York Pei; Elisabet Ars; Nuria Lloberas; Alvaro Madrid; Vikas R Dharnidharka; Anne M Connolly; Marcia C Willing; Megan A Cooper; Richard P Lifton; Matias Simons; Howard Riezman; Corinne Antignac; Julie D Saba; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2017-02-06       Impact factor: 14.808

6.  NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.

Authors:  Andrea Kerti; Rózsa Csohány; Attila Szabó; Ottó Arkossy; Péter Sallay; Vincent Moriniére; Virginia Vega-Warner; Gábor Nyírő; Orsolya Lakatos; Tamás Szabó; Beata S Lipska; Franz Schaefer; Corinne Antignac; George Reusz; Tivadar Tulassay; Kálmán Tory
Journal:  Pediatr Nephrol       Date:  2012-12-14       Impact factor: 3.714

7.  ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

Authors:  Heon Yung Gee; Pawaree Saisawat; Shazia Ashraf; Toby W Hurd; Virginia Vega-Warner; Humphrey Fang; Bodo B Beck; Olivier Gribouval; Weibin Zhou; Katrina A Diaz; Sivakumar Natarajan; Roger C Wiggins; Svjetlana Lovric; Gil Chernin; Dominik S Schoeb; Bugsu Ovunc; Yaacov Frishberg; Neveen A Soliman; Hanan M Fathy; Heike Goebel; Julia Hoefele; Lutz T Weber; Jeffrey W Innis; Christian Faul; Zhe Han; Joseph Washburn; Corinne Antignac; Shawn Levy; Edgar A Otto; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2013-07-08       Impact factor: 14.808

8.  A molecular mechanism explaining albuminuria in kidney disease.

Authors:  Bernhard Schermer; Thomas Benzing; Linus Butt; David Unnersjö-Jess; Martin Höhne; Aurelie Edwards; Julia Binz-Lotter; Dervla Reilly; Robert Hahnfeldt; Vera Ziegler; Katharina Fremter; Markus M Rinschen; Martin Helmstädter; Lena K Ebert; Hayo Castrop; Matthias J Hackl; Gerd Walz; Paul T Brinkkoetter; Max C Liebau; Kálmán Tory; Peter F Hoyer; Bodo B Beck; Hjalmar Brismar; Hans Blom
Journal:  Nat Metab       Date:  2020-05-11

9.  Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome.

Authors:  Jia Rao; Shazia Ashraf; Weizhen Tan; Amelie T van der Ven; Heon Yung Gee; Daniela A Braun; Krisztina Fehér; Sudeep P George; Amin Esmaeilniakooshkghazi; Won-Il Choi; Tilman Jobst-Schwan; Ronen Schneider; Johanna Magdalena Schmidt; Eugen Widmeier; Jillian K Warejko; Tobias Hermle; David Schapiro; Svjetlana Lovric; Shirlee Shril; Ankana Daga; Ahmet Nayir; Mohan Shenoy; Yincent Tse; Martin Bald; Udo Helmchen; Sevgi Mir; Afig Berdeli; Jameela A Kari; Sherif El Desoky; Neveen A Soliman; Arvind Bagga; Shrikant Mane; Mohamad A Jairajpuri; Richard P Lifton; Seema Khurana; Jose C Martins; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2017-10-23       Impact factor: 14.808

Review 10.  The renal biopsy in the genomic era.

Authors:  Helen Liapis; Joseph P Gaut
Journal:  Pediatr Nephrol       Date:  2012-11-21       Impact factor: 3.714

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.