B. Fogelgren

发表

Adeno-Associated Virus-Mediated Gene Transfer to Renal Tubule Cells via a Retrograde Ureteral Approach

J. Bennett, K. Park, J. Lipschutz, 2011, Nephron Extra.

Structural and functional diversity of lysyl oxidase and the LOX-like proteins.

S. Fong, K. Csiszȧr, J. Molnár, 2003, Biochimica et biophysica acta.

Transcriptional regulatory control of mammalian nephron progenitors revealed by multi-factor cistromic analysis and genetic studies

Sean M. Hasso, A. McMahon, B. Ren, 2018, PLoS genetics.

Regulation of Cell Polarity by Exocyst-Mediated Trafficking.

B. Fogelgren, N. Polgar, 2018, Cold Spring Harbor perspectives in biology.

The exocyst complex regulates insulin-stimulated glucose uptake of skeletal muscle cells.

M. Corley, B. Fogelgren, N. Polgar, 2019, American journal of physiology. Endocrinology and metabolism.

Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous system.

C. James, J. Biegel, L. Rorke, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Mutations of the INI 1 Rhabdoid Tumor Suppressor Gene in Medulloblastomas and Primitive Neuroectodermal Tumors of the Central Nervous System 1

C. James, J. Biegel, L. Rorke, 2000 .

Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor

J. Biegel, L. Rorke, Junhao Zhou, 2000, Genes, chromosomes & cancer.

Pan-Cancer Analyses Reveal Long Intergenic Non-Coding RNAs Relevant to Tumor Diagnosis, Subtyping and Prognosis

M. Tiirikainen, Herbert Yu, R. Fan, 2016, EBioMedicine.

The exocyst gene Sec10 regulates renal epithelial monolayer homeostasis and apoptotic sensitivity.

B. Fogelgren, Amanda J. Lee, N. Polgar, 2015, American journal of physiology. Cell physiology.

The Exocyst Protein Sec10 Interacts with Polycystin-2 and Knockdown Causes PKD-Phenotypes

K. Park, J. Lipschutz, R. Burdine, 2011, PLoS genetics.

Deletion of Orc4 during oogenesis severely reduces polar body extrusion and blocks zygotic DNA replication

Y. Yamazaki, B. Fogelgren, Hieu Nguyen, 2022, Biology of Reproduction.

Exocyst inactivation in urothelial cells disrupts autophagy and activates non-canonical NF-κB signaling

B. Fogelgren, Amanda J. Lee, M. Ortega, 2021, bioRxiv.

ENDOTHELIN-1 AND NA + , K + ATPASE GENE EXPRESSION IS UPREGULATED IN ADULT KIDNEYS OF A NOVEL MOUSE MODEL OF HERITABLE RENAL HYPOPLASIA , SUPPORTING DIAGNOSIS OF CHRONIC RENAL FAILURE Student

B. Fogelgren, S. Lozanoff, 2008 .

Isolation of genes from the rhabdoid tumor deletion region in chromosome band 22q11.2.

B. Roe, J. Biegel, Z. Wang, 2000, Gene.

Exocyst Sec10 Is Involved in Basolateral Protein Translation and Translocation in the Endoplasmic Reticulum

V. Lingappa, Soo‐Young Choi, J. Lipschutz, 2012, Nephron Experimental Nephrology.

The exocyst is required for photoreceptor ciliogenesis and retinal development

Seok-Hyung Kim, J. Lipschutz, R. Norris, 2017, The Journal of Biological Chemistry.

Conditional Loss of the Exocyst Component Exoc5 in Retinal Pigment Epithelium (RPE) Results in RPE Dysfunction, Photoreceptor Cell Degeneration, and Decreased Visual Function

J. Lipschutz, B. Fogelgren, Xiaofeng Zuo, 2021, International journal of molecular sciences.

Reduction in Wnt9b and associated gene expression in the embryonic midface of CL/Fr mice with heritable cleft lip and palate

B. Fogelgren, K. Fong, K. Nonaka, 2016 .

Exocyst Sec10 protects epithelial barrier integrity and enhances recovery following oxidative stress, by activation of the MAPK pathway.

K. Park, J. Lipschutz, Jinu Kim, 2010, American journal of physiology. Renal physiology.

Cellular Fibronectin Binds to Lysyl Oxidase with High Affinity and Is Critical for Its Proteolytic Activation*

K. Csiszȧr, B. Fogelgren, K. Fong, 2005, Journal of Biological Chemistry.

Discovery of protein-protein interactions of the lysyl oxidase enzyme : implications for cardiovascular disease, cancer and fibrosis

B. Fogelgren, 2005 .

Mutation in Mpzl3, a Gene Encoding a Predicted the Adhesion Protein, in the Rough Coat (rc) Mice with Severe Skin and Hair Abnormalities

K. Csiszȧr, P. Racz, B. Fogelgren, 2007 .

Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart.

K. Csiszȧr, B. Fogelgren, Subarna Khan, 2004, The Journal of investigative dermatology.

Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice

B. Fogelgren, Y. Marikawa, S. Lozanoff, 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.

J. Biegel, L. Rorke, B. Fogelgren, 1999, Cancer research.

A mutation in the tuft mouse disrupts TET1 activity and alters the expression of genes that are crucial for neural tube closure

Z. Ahmed, A. Maunakea, M. Corley, 2016, Disease Models & Mechanisms.

for neural tube closure in the tuft mouse

Z. Ahmed, A. Maunakea, M. Corley, 2016 .

Lysyl Oxidase Interacts with Hormone Placental Lactogen and Synergistically Promotes Breast Epithelial Cell Proliferation and Migration*

K. Csiszȧr, B. Fogelgren, N. Polgar, 2007, Journal of Biological Chemistry.

CALL FOR PAPERS Novel Therapeutics in Renal Diseases Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosis

K. Park, Soo‐Young Choi, J. Lipschutz, 2014 .

Novel Therapeutics in Renal Diseases Exocyst Sec 10 protects renal tubule cells from injury by EGFR / MAPK activation and effects on endocytosis

K. Park, Soo‐Young Choi, J. Lipschutz, 2014 .

Lysyl oxidase regulates breast cancer cell migration and adhesion through a hydrogen peroxide-mediated mechanism.

M. Hendrix, D. Kirschmann, E. Seftor, 2005, Cancer research.

Fibroproliferative response to urothelial failure obliterates the ureter lumen in a mouse model of prenatal congenital obstructive nephropathy

B. Fogelgren, Amanda J. Lee, N. Polgar, 2016, Scientific Reports.

Urothelial Defects from Targeted Inactivation of Exocyst Sec10 in Mice Cause Ureteropelvic Junction Obstructions

J. Lipschutz, B. Fogelgren, Xiaofeng Zuo, 2015, PloS one.

A novel human gene (SARM) at chromosome 17q11 encodes a protein with a SAM motif and structural similarity to Armadillo/beta-catenin that is conserved in mouse, Drosophila, and Caenorhabditis elegans.

K. Csiszȧr, B. Fogelgren, M. Mink, 2001, Genomics.

Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice.

Wenbin Ma, B. Fogelgren, C. Uyehara, 2009, American journal of physiology. Renal physiology.

Disruption of the exocyst induces podocyte loss and dysfunction

J. Lipschutz, D. Fermin, M. Sampson, 2019, The Journal of Biological Chemistry.

Arl13b and the exocyst interact synergistically in ciliogenesis

R. Kahn, Soo‐Young Choi, J. Lipschutz, 2016, Molecular biology of the cell.

Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.

Dongjun Chung, M. Heydarpour, S. Body, 2019, Circulation.

Primary cilia and the exocyst are linked to urinary extracellular vesicle production and content

M. Janech, J. Lipschutz, B. Fogelgren, 2019, The Journal of Biological Chemistry.

Drosophila Lysyl Oxidases Dmloxl-1 and Dmloxl-2 Are Differentially Expressed and the Active DmLOXL-1 Influences Gene Expression and Development*

S. Fong, K. Csiszȧr, D. Dooley, 2005, Journal of Biological Chemistry.

Osmoregulatory defect in adult mice associated with deficient prenatal expression of six2.

B. Fogelgren, S. Lozanoff, T. Hynd, 2011, American journal of physiology. Regulatory, integrative and comparative physiology.

Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing

J. Lipschutz, J. Bok, U. Kim, 2018, Molecular Neurobiology.

Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing

J. Lipschutz, J. Bok, U. Kim, 2018, Molecular Neurobiology.

A novel human lysyl oxidase-like gene (LOXL4) on chromosome 10q24 has an altered scavenger receptor cysteine rich domain.

S. Fong, K. Csiszȧr, B. Fogelgren, 2001, Matrix biology : journal of the International Society for Matrix Biology.

Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities.

K. Csiszȧr, P. Racz, B. Fogelgren, 2007, The Journal of investigative dermatology.

The Small GTPase Cdc42 Is Necessary for Primary Ciliogenesis in Renal Tubular Epithelial Cells*

J. Lipschutz, B. Fogelgren, Xiaofeng Zuo, 2011, The Journal of Biological Chemistry.

The exocyst gene Sec10 regulates renal epithelial monolayer homeostasis and apoptotic sensitivity.

B. Fogelgren, Amanda J. Lee, N. Polgar, 2015, American journal of physiology. Cell physiology.