APOL1 and APOL1-Associated Kidney Disease: A Common Disease, an Unusual Disease Gene − Proceedings of the Henry Shavelle Professorship

por Pollak, Martin R., Friedman, David J.
Publicado 2023

Disease Modeling with Kidney Organoids

por Karp, Sophie, Pollak, Martin R, Subramanian, Balajikarthick
Publicado 2022

Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing

por Brown, Elizabeth J., Pollak, Martin R., Barua, Moumita
Publicado 2014

The role of alpha-actinin-4 in human kidney disease

por Feng, Di, DuMontier, Clark, Pollak, Martin R
Publicado 2015

Improved IBD detection using incomplete haplotype information

por Genovese, Giulio, Leibon, Gregory, Pollak, Martin R, Rockmore, Daniel N
Publicado 2010

α-Actinin-4 Is Essential for Maintaining the Spreading, Motility and Contractility of Fibroblasts

por Shao, Hanshuang, Wang, James H.-C., Pollak, Martin R., Wells, Alan
Publicado 2010

Functional Validation of an Alpha-Actinin-4 Mutation as a Potential Cause of an Aggressive Presentation of Adolescent Focal Segmental Glomerulosclerosis: Implications for Genetic T...

por Feng, Di, Steinke, Julia M., Krishnan, Ramaswamy, Birrane, Gabriel, Pollak, Martin R.
Publicado 2016

SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity

por Carrasquillo, Robert, Tian, Dequan, Krishna, Sneha, Pollak, Martin R, Greka, Anna, Schlöndorff, Johannes
Publicado 2012

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis

por Barua, Moumita, Shieh, Eric, Schlondorff, Johannes, Genovese, Giulio, Kaplan, Bernard S, Pollak, Martin R
Publicado 2013

Human Kidney Disease-causing INF2 Mutations Perturb Rho/Dia Signaling in the Glomerulus

por Sun, Hua, Al-Romaih, Khaldoun I., MacRae, Calum A., Pollak, Martin R.
Publicado 2014

Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations

por Shao, Hanshuang, Wingert, Bentley, Weins, Astrid, Pollak, Martin R., Camacho, Carlos, Wells, Alan
Publicado 2019

Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis

por Barua, Moumita, Brown, Elizabeth J., Charoonratana, Victoria T., Genovese, Giulio, Sun, Hua, Pollak, Martin R.
Publicado 2012

Frequency of Rare Allelic Variation in Candidate Genes among Individuals with Low and High Urinary Calcium Excretion

por Toka, Hakan R., Genovese, Giulio, Mount, David B., Pollak, Martin R., Curhan, Gary C.
Publicado 2013

Clinical and Pathological Heterogeneity in FSGS due to INF2 Mutations

por Morales-Alvarez, Martha Catalina, Knob, Andrea, Rennke, Helmut G., Pollak, Martin R., Denker, Bradley M.
Publicado 2022

Autosomal Dominant Tubulointerstitial Kidney Disease—Uromodulin Misclassified as Focal Segmental Glomerulosclerosis or Hereditary Glomerular Disease

por Chun, Justin, Wang, Minxian, Wilkins, Maris S., Knob, Andrea U., Benjamin, Ava, Bu, Lihong, Pollak, Martin R.
Publicado 2020

The Calcium-Sensing Receptor Mediates Bone Turnover Induced by Dietary Calcium and Parathyroid Hormone in Neonates

por Shu, Lei, Ji, Ji, Zhu, Qi, Cao, Guofan, Karaplis, Andrew, Pollak, Martin R, Brown, Edward, Goltzman, David, Miao, Dengshun
Publicado 2011

α-Actinin-4-Mediated FSGS: An Inherited Kidney Disease Caused by an Aggregated and Rapidly Degraded Cytoskeletal Protein

por Yao, June, Le, Tu Cam, Kos, Claudine H, Henderson, Joel M, Allen, Phillip G, Denker, Bradley M, Pollak, Martin R
Publicado 2004

Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data

por Leykin, Igor, Hao, Ke, Cheng, Junsheng, Meyer, Nicole, Pollak, Martin R, Smith, Richard JH, Wong, Wing Hung, Rosenow, Carsten, Li, Cheng
Publicado 2005

Mutations in the formin protein INF2 cause focal segmental glomerulosclerosis

por Brown, Elizabeth J., Schlöndorff, Johannes S., Becker, Daniel J., Tsukaguchi, Hiroyasu, Uscinski, Andrea L., Higgs, Henry N., Henderson, Joel M., Pollak, Martin R.
Publicado 2009

Discovery of new glomerular disease-relevant genes by translational profiling of podocytes in vivo

por Grgic, Ivica, Hofmeister, Andreas F., Genovese, Giulio, Bernhardy, Andrea J., Sun, Hua, Maarouf, Omar H., Bijol, Vanesa, Pollak, Martin R., Humphreys, Benjamin D.
Publicado 2014