BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 35099763)

  • 21. NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome.
    Baylarov R; Senol O; Atan M; Berdeli A
    Saudi J Kidney Dis Transpl; 2020; 31(1):144-149. PubMed ID: 32129207
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
    Megremis S; Mitsioni A; Mitsioni AG; Fylaktou I; Kitsiou-Tzelli S; Stefanidis CJ; Kanavakis E; Traeger-Synodinos J
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):249-56. PubMed ID: 19371226
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
    Chernin G; Heeringa SF; Gbadegesin R; Liu J; Hinkes BG; Vlangos CN; Vega-Warner V; Hildebrandt F
    Pediatr Nephrol; 2008 Sep; 23(9):1455-60. PubMed ID: 18543005
    [TBL] [Abstract][Full Text] [Related]  

  • 24. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
    Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
    [TBL] [Abstract][Full Text] [Related]  

  • 25. NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
    Otukesh H; Ghazanfari B; Fereshtehnejad SM; Bakhshayesh M; Hashemi M; Hoseini R; Chalian M; Salami A; Mehdipor L; Rahiminia A
    Iran J Kidney Dis; 2009 Apr; 3(2):99-102. PubMed ID: 19395786
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
    Gbadegesin R; Hinkes B; Vlangos C; Mucha B; Liu J; Hopcian J; Hildebrandt F
    Pediatr Nephrol; 2007 Apr; 22(4):509-13. PubMed ID: 17216259
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
    Li Y; He Q; Wang Y; Dang X; Wu X; Li X; Shuai L; Yi Z
    Ann Clin Lab Sci; 2019 May; 49(3):330-337. PubMed ID: 31308032
    [TBL] [Abstract][Full Text] [Related]  

  • 28. NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.
    Mao J; Zhang Y; Du L; Dai Y; Gu W; Liu A; Shang S; Liang L
    Pediatr Res; 2007 Jan; 61(1):117-22. PubMed ID: 17211152
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients.
    Ozçakar ZB; Cengiz FB; Cakar N; Uncu N; Kara N; Acar B; Yüksel S; Ekim M; Tekin M; Yalçinkaya F
    Pediatr Nephrol; 2006 Aug; 21(8):1093-6. PubMed ID: 16810518
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
    Rood IM; Deegens JKJ; Lugtenberg D; Bongers EMHF; Wetzels JFM
    Am J Kidney Dis; 2019 Mar; 73(3):400-403. PubMed ID: 30241959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Kidney Organoids Generated Using an Allelic Series of NPHS2 Point Variants Reveal Distinct Intracellular Podocin Mistrafficking.
    Dorison A; Ghobrial I; Graham A; Peiris T; Forbes TA; See M; Das M; Saleem MA; Quinlan C; Lawlor KT; Ramialison M; Howden SE; Little MH
    J Am Soc Nephrol; 2023 Jan; 34(1):88-109. PubMed ID: 36167728
    [TBL] [Abstract][Full Text] [Related]  

  • 32. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
    Basiratnia M; Yavarian M; Torabinezhad S; Erjaee A
    Iran J Kidney Dis; 2013 Sep; 7(5):357-62. PubMed ID: 24072147
    [TBL] [Abstract][Full Text] [Related]  

  • 33. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K; Iijima K; Ikeda M; Kitamura A; Tsukaguchi H; Yoshiya K; Hoshii S; Wada N; Uemura O; Satomura K; Honda M; Yoshikawa N
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.
    Carrasco-Miranda JS; Garcia-Alvarez R; Sotelo-Mundo RR; Valenzuela O; Islas-Osuna MA; Sotelo-Cruz N
    Genet Mol Res; 2013 Jun; 12(2):2102-7. PubMed ID: 23913389
    [TBL] [Abstract][Full Text] [Related]  

  • 35. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
    Ramanathan AS; Vijayan M; Rajagopal S; Rajendiran P; Senguttuvan P
    Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
    [TBL] [Abstract][Full Text] [Related]  

  • 36. NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
    Kerti A; Csohány R; Szabó A; Arkossy O; Sallay P; Moriniére V; Vega-Warner V; Nyírő G; Lakatos O; Szabó T; Lipska BS; Schaefer F; Antignac C; Reusz G; Tulassay T; Tory K
    Pediatr Nephrol; 2013 May; 28(5):751-7. PubMed ID: 23242530
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains.
    Huber TB; Simons M; Hartleben B; Sernetz L; Schmidts M; Gundlach E; Saleem MA; Walz G; Benzing T
    Hum Mol Genet; 2003 Dec; 12(24):3397-405. PubMed ID: 14570703
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
    Wang F; Zhang Y; Mao J; Yu Z; Yi Z; Yu L; Sun J; Wei X; Ding F; Zhang H; Xiao H; Yao Y; Tan W; Lovric S; Ding J; Hildebrandt F
    Pediatr Nephrol; 2017 Jul; 32(7):1181-1192. PubMed ID: 28204945
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
    Machuca E; Hummel A; Nevo F; Dantal J; Martinez F; Al-Sabban E; Baudouin V; Abel L; Grünfeld JP; Antignac C
    Kidney Int; 2009 Apr; 75(7):727-35. PubMed ID: 19145239
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.
    Thomas MM; Ahmed HM; El-Dessouky SH; Ramadan A; Botrous OE; Abdel-Hamid MS
    Mol Genet Genomics; 2022 May; 297(3):689-698. PubMed ID: 35278126
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.