Auteur zoekresultaten

1

Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases door Kristopher T. Kahle, Jesse Rinehart, Richard P. Lifton

Gepubliceerd in 2010

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2

Molecular Mechanisms of Human Hypertension door Richard P. Lifton, Ali G. Gharavi, David S. Geller

Gepubliceerd in 2001

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3

In vivo phosphorylation of the epithelial sodium channel door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

Gepubliceerd in 1998

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4

The Activity of the Epithelial Sodium Channel Is Regulated by Clathrin-mediated Endocytosis door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

Gepubliceerd in 1997

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Artigo

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5

Rare mutations in the human Na-K-Cl cotransporter (NKCC2) associated with lower blood pressure exhibit impaired processing and transport function door Michelle Y. Monette, Jesse Rinehart, Richard P. Lifton, Biff Forbush

Gepubliceerd in 2011

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Artigo

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6

Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4 door Shigeru Shibata, Junhui Zhang, Jeremy Puthumana, Kathryn L. Stone, Richard P. Lifton

Gepubliceerd in 2013

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Artigo

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7

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism door David S. Geller, Junhui Zhang, Max Wisgerhof, Cedric Shackleton, Michael Kashgarian, Richard P. Lifton

Gepubliceerd in 2008

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Artigo

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8

Structure of the 5'-flanking regulatory region and gene for the human growth factor-activatable Na/H exchanger NHE-1 door R. Tyler Miller, Laurent Counillon, Gilles Pagès, Richard P. Lifton, Claude Sardet, Jacques Pouysségur

Gepubliceerd in 1991

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Artigo

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9

Identification of a PY motif in the epithelial Na channel subunits as a target sequence for mutations causing channel activation found in Liddle syndrome. door Laurent Schild, Yin Lu, Ivan Gautschi, Estelle Schneeberger, Richard P. Lifton, Bernard C. Rossier

Gepubliceerd in 1996

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Artigo

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10

Exclusion of the Na(+)-H+ antiporter as a candidate gene in human essential hypertension. door Richard P. Lifton, Steven C. Hunt, R R Williams, Jacques Pouysségur, Jean-Marc Lalouel

Gepubliceerd in 1991

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Artigo

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11

Evaluation of the Dexamethasone Suppression Test for the Diagnosis of Glucocorticoid-Remediable Aldosteronism1 door W. Reid Litchfield, Maria I. New, Caroline Coolidge, Richard P. Lifton, Robert G. Dluhy

Gepubliceerd in 1997

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Artigo

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12

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl − -transporting epithelia door Keith A. Choate, Kristopher T. Kahle, Frederick H. Wilson, Carol Nelson‐Williams, Richard P. Lifton

Gepubliceerd in 2003

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Artigo

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13

Intracranial Aneurysm and Hemorrhagic Stroke in Glucocorticoid-remediable Aldosteronism door W. Reid Litchfield, Bruce F. Anderson, Ruediger J. Weiss, Richard P. Lifton, Robert G. Dluhy

Gepubliceerd in 1998

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14

Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life door Dinna N. Cruz, Andrea J. Shaer, Margaret J. Bia, Richard P. Lifton, David B. Simon

Gepubliceerd in 2001

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Artigo

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15

Potassium depletion stimulates Na-Cl cotransporter via phosphorylation and inactivation of the ubiquitin ligase Kelch-like 3 door Kenichi Ishizawa, Ning Xu, Johannes Loffing, Richard P. Lifton, Toshiro Fujita, Shunya Uchida, Shigeru Shibata

Gepubliceerd in 2016

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Artigo

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16

Serial exome analysis of disease progression in premalignant gammopathies door Siming Zhao, Hojung Choi, Christoph Heuck, Shrikant Mane, B Barlogie, Richard P. Lifton, Madhav V. Dhodapkar

Gepubliceerd in 2014

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Carta

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17

Genetic Influence on Neurodevelopment in Nonsyndromic Craniosynostosis door Andrew T. Timberlake, Alexandra Junn, Roberto L. Flores, David A. Staffenberg, Richard P. Lifton, John A. Persing

Gepubliceerd in 2022

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Artigo

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18

An SGK1 site in WNK4 regulates Na + channel and K + channel activity and has implications for aldosterone signaling and K + homeostasis door Aaron M. Ring, Qiang Leng, Jesse Rinehart, Frederick H. Wilson, Kristopher T. Kahle, Steven Hébert, Richard P. Lifton

Gepubliceerd in 2007

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19

Regression of Chemotherapy-Resistant Polymerase ϵ (POLE) Ultra-Mutated and MSH6 Hyper-Mutated Endometrial Tumors with Nivolumab door Alessandro D. Santin, Stefania Bellone, Natália Buza, Jungmin Choi, Peter E. Schwartz, Joseph Schlessinger, Richard P. Lifton

Gepubliceerd in 2016

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20

Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing door M. Kyle Cromer, Lee F. Starker, Murim Choi, Robert Udelsman, Carol Nelson‐Williams, Richard P. Lifton, Tobias Carling

Gepubliceerd in 2012

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Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases door Kristopher T. Kahle, Jesse Rinehart, Richard P. Lifton

Molecular Mechanisms of Human Hypertension door Richard P. Lifton, Ali G. Gharavi, David S. Geller

<i>In vivo</i> phosphorylation of the epithelial sodium channel door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

The Activity of the Epithelial Sodium Channel Is Regulated by Clathrin-mediated Endocytosis door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

Rare mutations in the human Na-K-Cl cotransporter (NKCC2) associated with lower blood pressure exhibit impaired processing and transport function door Michelle Y. Monette, Jesse Rinehart, Richard P. Lifton, Biff Forbush

Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4 door Shigeru Shibata, Junhui Zhang, Jeremy Puthumana, Kathryn L. Stone, Richard P. Lifton

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism door David S. Geller, Junhui Zhang, Max Wisgerhof, Cedric Shackleton, Michael Kashgarian, Richard P. Lifton

Structure of the 5'-flanking regulatory region and gene for the human growth factor-activatable Na/H exchanger NHE-1 door R. Tyler Miller, Laurent Counillon, Gilles Pagès, Richard P. Lifton, Claude Sardet, Jacques Pouysségur

Identification of a PY motif in the epithelial Na channel subunits as a target sequence for mutations causing channel activation found in Liddle syndrome. door Laurent Schild, Yin Lu, Ivan Gautschi, Estelle Schneeberger, Richard P. Lifton, Bernard C. Rossier

Exclusion of the Na(+)-H+ antiporter as a candidate gene in human essential hypertension. door Richard P. Lifton, Steven C. Hunt, R R Williams, Jacques Pouysségur, Jean-Marc Lalouel

Evaluation of the Dexamethasone Suppression Test for the Diagnosis of Glucocorticoid-Remediable Aldosteronism1 door W. Reid Litchfield, Maria I. New, Caroline Coolidge, Richard P. Lifton, Robert G. Dluhy

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl <sup>−</sup> -transporting epithelia door Keith A. Choate, Kristopher T. Kahle, Frederick H. Wilson, Carol Nelson‐Williams, Richard P. Lifton

Intracranial Aneurysm and Hemorrhagic Stroke in Glucocorticoid-remediable Aldosteronism door W. Reid Litchfield, Bruce F. Anderson, Ruediger J. Weiss, Richard P. Lifton, Robert G. Dluhy

Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life door Dinna N. Cruz, Andrea J. Shaer, Margaret J. Bia, Richard P. Lifton, David B. Simon

Potassium depletion stimulates Na-Cl cotransporter via phosphorylation and inactivation of the ubiquitin ligase Kelch-like 3 door Kenichi Ishizawa, Ning Xu, Johannes Loffing, Richard P. Lifton, Toshiro Fujita, Shunya Uchida, Shigeru Shibata

Serial exome analysis of disease progression in premalignant gammopathies door Siming Zhao, Hojung Choi, Christoph Heuck, Shrikant Mane, B Barlogie, Richard P. Lifton, Madhav V. Dhodapkar

Genetic Influence on Neurodevelopment in Nonsyndromic Craniosynostosis door Andrew T. Timberlake, Alexandra Junn, Roberto L. Flores, David A. Staffenberg, Richard P. Lifton, John A. Persing

An SGK1 site in WNK4 regulates Na <sup>+</sup> channel and K <sup>+</sup> channel activity and has implications for aldosterone signaling and K <sup>+</sup> homeostasis door Aaron M. Ring, Qiang Leng, Jesse Rinehart, Frederick H. Wilson, Kristopher T. Kahle, Steven Hébert, Richard P. Lifton

Regression of Chemotherapy-Resistant Polymerase ϵ (POLE) Ultra-Mutated and MSH6 Hyper-Mutated Endometrial Tumors with Nivolumab door Alessandro D. Santin, Stefania Bellone, Natália Buza, Jungmin Choi, Peter E. Schwartz, Joseph Schlessinger, Richard P. Lifton

Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing door M. Kyle Cromer, Lee F. Starker, Murim Choi, Robert Udelsman, Carol Nelson‐Williams, Richard P. Lifton, Tobias Carling

Zoekresultaten - Richard P. Lifton

Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases door Kristopher T. Kahle, Jesse Rinehart, Richard P. Lifton

Molecular Mechanisms of Human Hypertension door Richard P. Lifton, Ali G. Gharavi, David S. Geller

<i>In vivo</i> phosphorylation of the epithelial sodium channel door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

The Activity of the Epithelial Sodium Channel Is Regulated by Clathrin-mediated Endocytosis door Richard A. Shimkets, Richard P. Lifton, Cecilia M. Canessa

Rare mutations in the human Na-K-Cl cotransporter (NKCC2) associated with lower blood pressure exhibit impaired processing and transport function door Michelle Y. Monette, Jesse Rinehart, Richard P. Lifton, Biff Forbush

Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4 door Shigeru Shibata, Junhui Zhang, Jeremy Puthumana, Kathryn L. Stone, Richard P. Lifton

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism door David S. Geller, Junhui Zhang, Max Wisgerhof, Cedric Shackleton, Michael Kashgarian, Richard P. Lifton

Structure of the 5'-flanking regulatory region and gene for the human growth factor-activatable Na/H exchanger NHE-1 door R. Tyler Miller, Laurent Counillon, Gilles Pagès, Richard P. Lifton, Claude Sardet, Jacques Pouysségur

Identification of a PY motif in the epithelial Na channel subunits as a target sequence for mutations causing channel activation found in Liddle syndrome. door Laurent Schild, Yin Lu, Ivan Gautschi, Estelle Schneeberger, Richard P. Lifton, Bernard C. Rossier

Exclusion of the Na(+)-H+ antiporter as a candidate gene in human essential hypertension. door Richard P. Lifton, Steven C. Hunt, R R Williams, Jacques Pouysségur, Jean-Marc Lalouel

Evaluation of the Dexamethasone Suppression Test for the Diagnosis of Glucocorticoid-Remediable Aldosteronism1 door W. Reid Litchfield, Maria I. New, Caroline Coolidge, Richard P. Lifton, Robert G. Dluhy

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl <sup>−</sup> -transporting epithelia door Keith A. Choate, Kristopher T. Kahle, Frederick H. Wilson, Carol Nelson‐Williams, Richard P. Lifton

Intracranial Aneurysm and Hemorrhagic Stroke in Glucocorticoid-remediable Aldosteronism door W. Reid Litchfield, Bruce F. Anderson, Ruediger J. Weiss, Richard P. Lifton, Robert G. Dluhy

Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life door Dinna N. Cruz, Andrea J. Shaer, Margaret J. Bia, Richard P. Lifton, David B. Simon

Potassium depletion stimulates Na-Cl cotransporter via phosphorylation and inactivation of the ubiquitin ligase Kelch-like 3 door Kenichi Ishizawa, Ning Xu, Johannes Loffing, Richard P. Lifton, Toshiro Fujita, Shunya Uchida, Shigeru Shibata

Serial exome analysis of disease progression in premalignant gammopathies door Siming Zhao, Hojung Choi, Christoph Heuck, Shrikant Mane, B Barlogie, Richard P. Lifton, Madhav V. Dhodapkar

Genetic Influence on Neurodevelopment in Nonsyndromic Craniosynostosis door Andrew T. Timberlake, Alexandra Junn, Roberto L. Flores, David A. Staffenberg, Richard P. Lifton, John A. Persing

An SGK1 site in WNK4 regulates Na <sup>+</sup> channel and K <sup>+</sup> channel activity and has implications for aldosterone signaling and K <sup>+</sup> homeostasis door Aaron M. Ring, Qiang Leng, Jesse Rinehart, Frederick H. Wilson, Kristopher T. Kahle, Steven Hébert, Richard P. Lifton

Regression of Chemotherapy-Resistant Polymerase ϵ (POLE) Ultra-Mutated and MSH6 Hyper-Mutated Endometrial Tumors with Nivolumab door Alessandro D. Santin, Stefania Bellone, Natália Buza, Jungmin Choi, Peter E. Schwartz, Joseph Schlessinger, Richard P. Lifton

Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing door M. Kyle Cromer, Lee F. Starker, Murim Choi, Robert Udelsman, Carol Nelson‐Williams, Richard P. Lifton, Tobias Carling

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