These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 26940125)

  • 1. Contribution of the TTC21B gene to glomerular and cystic kidney diseases.
    Bullich G; Vargas I; Trujillano D; Mendizábal S; Piñero-Fernández JA; Fraga G; García-Solano J; Ballarín J; Estivill X; Torra R; Ars E
    Nephrol Dial Transplant; 2017 Jan; 32(1):151-156. PubMed ID: 26940125
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in TTC21B cause different phenotypes in two childhood cases in China.
    Zhang H; Su B; Liu X; Xiao H; Ding J; Yao Y
    Nephrology (Carlton); 2018 Apr; 23(4):371-376. PubMed ID: 28124483
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS.
    Huynh Cong E; Bizet AA; Boyer O; Woerner S; Gribouval O; Filhol E; Arrondel C; Thomas S; Silbermann F; Canaud G; Hachicha J; Ben Dhia N; Peraldi MN; Harzallah K; Iftene D; Daniel L; Willems M; Noel LH; Bole-Feysot C; Nitschké P; Gubler MC; Mollet G; Saunier S; Antignac C
    J Am Soc Nephrol; 2014 Nov; 25(11):2435-43. PubMed ID: 24876116
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Medullary Cystic Kidney Disease and Focal Segmental Glomerulosclerosis Caused by a Compound Heterozygous Mutation in TTC21B.
    Hibino S; Morisada N; Takeda A; Tanaka K; Nozu K; Yamakawa S; Iijima K; Fujita N
    Intern Med; 2020 Jul; 59(14):1735-1738. PubMed ID: 32238723
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Compound Heterozygous Mutation in the Ciliary Gene
    Abo El Fotoh WMM; Al-Fiky AF
    J Pediatr Genet; 2020 Sep; 9(3):198-202. PubMed ID: 32714622
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease.
    Fan LL; Liu L; Luo FM; Du R; Wang CY; Dong Y; Liu JS
    Mol Genet Genomic Med; 2020 Dec; 8(12):e1545. PubMed ID: 33159707
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical features and TTC21B genotype of a child with nephronophthisis type 12].
    Jian S; Wei QJ; Liu YT; Wang W; Zhou Y; Quan MY; He YY; Song HM; Wei M
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 Jun; 21(6):580-584. PubMed ID: 31208513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney disease.
    Olinger E; Phakdeekitcharoen P; Caliskan Y; Orr S; Mabillard H; Pickles C; Tse Y; Wood K; ; Sayer JA
    Am J Med Genet C Semin Med Genet; 2022 Mar; 190(1):109-120. PubMed ID: 35289079
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.
    Büscher AK; Celebi N; Hoyer PF; Klein HG; Weber S; Hoefele J
    Pediatr Nephrol; 2018 Mar; 33(3):433-437. PubMed ID: 29038887
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum disease.
    Strong A; Li D; Mentch F; Hakonarson H
    Am J Med Genet A; 2021 Apr; 185(4):1266-1269. PubMed ID: 33547761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Kidney Injury by Variants in the
    Frese J; Kettwig M; Zappel H; Hofer J; Gröne HJ; Nagel M; Sunder-Plassmann G; Kain R; Neuweiler J; Gross O
    Int J Mol Sci; 2019 Jan; 20(3):. PubMed ID: 30691124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis.
    Mistry K; Ireland JH; Ng RC; Henderson JM; Pollak MR
    Am J Kidney Dis; 2007 Nov; 50(5):855-64. PubMed ID: 17954299
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
    Büscher AK; Konrad M; Nagel M; Witzke O; Kribben A; Hoyer PF; Weber S
    Clin Nephrol; 2012 Jul; 78(1):47-53. PubMed ID: 22732337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tubuloglomerular Disease With Cone-Shaped Epiphyses Associated With Hypomorphic Variant and a Novel p.Cys14Arg in the
    Bezdíčka M; Zemková D; Skálová S; Hovorková E; Podhola M; Burkert J; Zieg J
    Front Pediatr; 2021; 9():752878. PubMed ID: 34805047
    [TBL] [Abstract][Full Text] [Related]  

  • 15. NPHS2 gene polymorphism aggravates renal damage caused by focal segmental glomerulosclerosis with COL4A3 mutation.
    Sun L; Zhang X; Wang Z
    Biosci Rep; 2021 Jan; 41(1):. PubMed ID: 33305316
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure.
    Stefanou C; Pieri M; Savva I; Georgiou G; Pierides A; Voskarides K; Deltas C
    Nephron; 2015; 130(3):200-12. PubMed ID: 26138234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
    Kerti A; Csohány R; Wagner L; Jávorszky E; Maka E; Tory K
    Pediatr Nephrol; 2013 Oct; 28(10):2061-4. PubMed ID: 23800802
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable renal phenotype in a family with an INF2 mutation.
    Lee HK; Han KH; Jung YH; Kang HG; Moon KC; Ha IS; Choi Y; Cheong HI
    Pediatr Nephrol; 2011 Jan; 26(1):73-6. PubMed ID: 20803156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. COL4A3 mutations cause focal segmental glomerulosclerosis.
    Xie J; Wu X; Ren H; Wang W; Wang Z; Pan X; Hao X; Tong J; Ma J; Ye Z; Meng G; Zhu Y; Kiryluk K; Kong X; Hu L; Chen N
    J Mol Cell Biol; 2014 Dec; 6(6):498-505. PubMed ID: 25596306
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
    Laurin LP; Lu M; Mottl AK; Blyth ER; Poulton CJ; Weck KE
    Nephrol Dial Transplant; 2014 Nov; 29(11):2062-9. PubMed ID: 24500309
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.