Search Results - "Lavin, Peter J"

Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous haemodiafiltration (CVVHDF) by Kirwan, Marcus, Munshi, Reema, O'Keeffe, Hannah, Judge, Conor, Coyle, Mary, Deasy, Evelyn, Kelly, Yvelynne P, Lavin, Peter J, Donnelly, Maria, D'Arcy, Deirdre M

“…Therapeutic antibiotic dose monitoring can be particularly challenging in septic patients requiring renal replacement therapy. Our aim was to conduct an…”
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A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy by MALIK, Talat H, LAVIN, Peter J, PICKERING, Matthew C, GOICOECHEA DE JORGE, Elena, VERNON, Katherine A, ROSE, Kirsten L, PATEL, Mitali P, DE LEEUW, Marcel, NEARLY, John J, COLON, Peter J, WINN, Michelle P

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TRPC6 Enhances Angiotensin II-induced Albuminuria by ECKEL, Jason, LAVIN, Peter J, SPARKS, Matthew, ZHU SHAN ZHANG, HOMSTAD, Alison, BARISONI, Laura, BIRBAUMER, Lutz, ROSENBERG, Paul, WINN, Michelle P, FINCH, Elizabeth A, MUKERJI, Nirvan, BURCH, Jarrett, GBADEGESIN, Rasheed, GUANGHONG WU, BOWLING, Brandy, BYRD, Alison, HALL, Gentzon

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Therapeutic targets in focal and segmental glomerulosclerosis by Lavin, Peter J, Gbadegesin, Rasheed, Damodaran, Tirupapuliyur V, Winn, Michelle P

“…PURPOSE OF REVIEWFocal and segmental glomerulosclerosis occurs due to a defect in the glomerular filtration barrier. This review highlights contributions from…”
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A hybrid CFHR3-1 gene causes familial C3 glomerulopathy by Malik, Talat H, Lavin, Peter J, Goicoechea de Jorge, Elena, Vernon, Katherine A, Rose, Kirsten L, Patel, Mitali P, de Leeuw, Marcel, Neary, John J, Conlon, Peter J, Winn, Michelle P, Pickering, Matthew C

“…Controlled activation of the complement system, a key component of innate immunity, enables destruction of pathogens with minimal damage to host tissue…”
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TRPC6 enhances angiotensin II-induced albuminuria by Eckel, Jason, Lavin, Peter J, Finch, Elizabeth A, Mukerji, Nirvan, Burch, Jarrett, Gbadegesin, Rasheed, Wu, Guanghong, Bowling, Brandy, Byrd, Alison, Hall, Gentzon, Sparks, Matthew, Zhang, Zhu Shan, Homstad, Alison, Barisoni, Laura, Birbaumer, Lutz, Rosenberg, Paul, Winn, Michelle P

“…Mutations in the canonical transient receptor potential cation channel 6 (TRPC6) are responsible for familial forms of adult onset focal segmental…”
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Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis by Gbadegesin, Rasheed A, Lavin, Peter J, Hall, Gentzon, Bartkowiak, Bartlomiej, Homstad, Alison, Jiang, Ruiji, Wu, Guanghong, Byrd, Alison, Lynn, Kelvin, Wolfish, Norman, Ottati, Carolina, Stevens, Paul, Howell, David, Conlon, Peter, Winn, Michelle P

“…Focal and segmental glomerulosclerosis (FSGS) is a major cause of end-stage kidney disease. Recent advances in molecular genetics show that defects in the…”
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Neurons that regulate mouse torpor by Hrvatin, Sinisa, Sun, Senmiao, Wilcox, Oren F., Yao, Hanqi, Lavin-Peter, Aurora J., Cicconet, Marcelo, Assad, Elena G., Palmer, Michaela E., Aronson, Sage, Banks, Alexander S., Griffith, Eric C., Greenberg, Michael E.

“…The advent of endothermy, which is achieved through the continuous homeostatic regulation of body temperature and metabolism 1 , 2 , is a defining feature of…”
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Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector by Luo, Xiaoyan, Hall, Gentzon, Li, Songtao, Bird, Andrew, Lavin, Peter J, Winn, Michelle P, Kemper, Alex R, Brown, Talmage T, Koeberl, Dwight D

“…Glycogen storage disease type Ia (GSD-Ia) is caused by the deficiency of glucose-6-phosphatase (G6Pase). Long-term complications of GSD-Ia include…”
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TORCing up the importance of calcium signaling by Lavin, Peter J, Winn, Michelle P

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Kidney transplant outcomes in familial C3 glomerulopathy by Wong, Limy, Moran, Sarah, Lavin, Peter J., Dorman, Anthony M., Conlon, Peter J.

“…C3 glomerulopathy, a newly designated entity, is characterized by glomerular disease associated with dysregulation of the alternative complement pathway and is…”
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Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS by Gbadegesin, Rasheed, Bartkowiak, Bartlomiej, Lavin, Peter J., Mukerji, Nirvan, Wu, Guanghong, Bowling, Brandy, Eckel, Jason, Damodaran, Tirupapuliyur, Winn, Michelle P.

“…Focal and segmental glomerulosclerosis (FSGS) is the most common glomerular cause of end-stage kidney disease (ESKD). Although the etiology of FSGS has not…”
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Monogenic causes of chronic kidney disease in adults by Connaughton, Dervla M, Kennedy, Claire, Shril, Shirlee, Mann, Nina, Murray, Susan L, Williams, Patrick A, Conlon, Eoin, Nakayama, Makiko, van der Ven, Amelie T, Ityel, Hadas, Kause, Franziska, Kolvenbach, Caroline M, Dai, Rufeng, Vivante, Asaf, Braun, Daniela A, Schneider, Ronen, Kitzler, Thomas M, Moloney, Brona, Moran, Conor P, Smyth, John S, Kennedy, Alan, Benson, Katherine, Stapleton, Caragh, Denton, Mark, Magee, Colm, O'Seaghdha, Conall M, Plant, William D, Griffin, Matthew D, Awan, Atif, Sweeney, Clodagh, Mane, Shrikant M, Lifton, Richard P, Griffin, Brenda, Leavey, Sean, Casserly, Liam, de Freitas, Declan G, Holian, John, Dorman, Anthony, Doyle, Brendan, Lavin, Peter J, Little, Mark A, Conlon, Peter J, Hildebrandt, Friedhelm

“…Approximately 500 monogenic causes of chronic kidney disease (CKD) have been identified, mainly in pediatric populations. The frequency of monogenic causes…”
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Prevention of sudden cardiac death in hemodialysis patients by O'Shaughnessy, Michelle M, O'Regan, John A, Lavin, Peter J

“…One quarter of all hemodialysis patients will succumb to sudden cardiac death (SCD), a rate far exceeding that observed in the general population. A high…”
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INVERTED FORMIN 2 MUTATIONS WITH VARIABLE EXPRESION IN PATIENTS WITH SPORADIC AND HEREDITARY FOCAL AND SEGMENTAL GLOMERULOSCLEROSIS by Gbadegesin, Rasheed, Lavin, Peter J., Hall, Gentzon, Bartkowiak, B, Homstad, A, Jiang, R, Wu, G, Byrd, A, Lynn, Kelvin, Wolfish, Norman, Ottati, Carolina, Stevens, Paul, Howell, David, Conlon, Peter, Winn, Michelle P.

“…Focal and segmental glomerulosclerosis (FSGS) is a major cause of end-stage kidney disease. Recent advances in molecular genetics show that defects in the…”
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Exclusion of homozygous PLCE1 by Mukerji, Nirvan, Gbadegesin, Rasheed, Bartkowiak, Bartlomiej, Lavin, Peter J, Bowling, Brandy, Winn, Michelle P, Wu, Guanghong, Damodaran, Tirupapuliyur, Eckel, Jason

“…Focal and segmental glomerulosclerosis (FSGS) is the most common glomerular cause of end-stage kidney disease (ESKD). Although the etiology of FSGS has not…”
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Kidney transplant outcomes in familial C3 glomerulopathy by Wong, Limy, Moran, Sarah, Lavin, Peter J, Dorman, Anthony M, Conlon, Peter J

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