[PDF][PDF] Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms

TA Forbes, SE Howden, K Lawlor, B Phipson… - The American Journal of …, 2018 - cell.com
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms.

TA Forbes, SE Howden, K Lawlor… - American Journal of …, 2018 - europepmc.org
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

[HTML][HTML] Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

TA Forbes, SE Howden, K Lawlor… - American Journal of …, 2018 - ncbi.nlm.nih.gov
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms

TA Forbes, SE Howden, K Lawlor… - … Journal of Human …, 2018 - researchonline.jcu.edu.au
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remainsunresolved. Kidney organoids differentiated …

[引用][C] Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

TA Forbes, SE Howden, K Lawlor, B Phipson… - The American Journal …, 2018 - cir.nii.ac.jp
Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal
Phenotype and Reveal Underlying Pathogenetic Mechanisms | CiNii Research CiNii 国立 …

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

TA Forbes, SE Howden, K Lawlor… - … journal of human …, 2018 - pubmed.ncbi.nlm.nih.gov
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

[引用][C] Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms

TA Forbes, SE Howden, K Lawlor… - … Journal of Human …, 2018 - espace.library.uq.edu.au
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

[HTML][HTML] Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

TA Forbes, SE Howden, K Lawlor, B Phipson… - The American Journal of …, 2018 - Elsevier
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remains unresolved. Kidney organoids differentiated …

Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms

TA Forbes, SE Howden, K Lawlor… - … Journal of Human …, 2018 - researchonline.jcu.edu.au
Despite the increasing diagnostic rate of genomic sequencing, the genetic basis of more
than 50% of heritable kidney disease remainsunresolved. Kidney organoids differentiated …