Lifton, Richard P.
Richard P. Lifton American biochemist and president of Rockefeller University
Richard P. Lifton American biochemist
VIAF ID: 271376104 (Personal)
Permalink: http://viaf.org/viaf/271376104
Preferred Forms
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100 1 _ ‡a Lifton, Richard P.
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100 1 _ ‡a Lifton, Richard P.
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100 1 _
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Lifton, Richard P.
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100 1 _ ‡a Lifton, Richard P. (sparse)
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100 1 _ ‡a Lifton, Richard P.
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100 1 _
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Lifton, Richard P.
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100 1 _
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Lifton, Richard P.
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Richard P. Lifton
‡c
American biochemist
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100 0 _
‡a
Richard P. Lifton
‡c
American biochemist and president of Rockefeller University
4xx's: Alternate Name Forms (11)
5xx's: Related Names (1)
Works
| Title | Sources |
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| ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment |
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| Angiotensin II signaling increases activity of the renal Na-Cl cotransporter through a WNK4-SPAK-dependent pathway |
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| Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease |
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| The B1-subunit of the H(+) ATPase is required for maximal urinary acidification |
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| DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling |
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| Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens |
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| Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome |
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| A form of the metabolic syndrome associated with mutations in DYRK1B |
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| Genes and environment in neonatal intraventricular hemorrhage |
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| The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities |
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| Genetic diagnosis by whole exome capture and massively parallel DNA sequencing |
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| Genetic diseases of the kidney / ed. by Richard P. Lifton. - Amsterdam, 2009. |
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| Genetic studies of body mass index yield new insights for obesity biology |
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| Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae |
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| Genome-wide association study of intracranial aneurysm identifies three new risk loci |
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| High bone density due to a mutation in LDL-receptor-related protein 5 |
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| Increased Levels of Macrophage Inflammatory Proteins Result in Resistance to R5-Tropic HIV-1 in a Subset of Elite Controllers. |
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| Individual exome analysis in diagnosis and management of paediatric liver failure of indeterminate aetiology |
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| Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4 |
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| KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein |
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| Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis |
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| Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy |
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| Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13 |
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| Mice lacking the B1 subunit of H+ -ATPase have normal hearing |
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| Molecular cloning and characterization of Atp6v1b1, the murine vacuolar H+-ATPase B1-subunit |
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| Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders |
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| Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4 |
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| Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism |
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| Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome |
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| Mutations in SEC63 cause autosomal dominant polycystic liver disease |
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| Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development |
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| Of hearts and hypertension, 1998: |
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| Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis |
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| A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum |
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| Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. |
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| Rare independent mutations in renal salt handling genes contribute to blood pressure variation |
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| Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome |
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| Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension |
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| Sequence variants in SLITRK1 are associated with Tourette's syndrome |
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| An SGK1 site in WNK4 regulates Na+ channel and K+ channel activity and has implications for aldosterone signaling and K+ homeostasis |
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| Skint-1 is a highly specific, unique selecting component for epidermal T cells |
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| Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal gammadelta T cells |
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| Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi |
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| Susceptibility loci for intracranial aneurysm in European and Japanese populations |
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| Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations |
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| WNK3 kinase is a positive regulator of NKCC2 and NCC, renal cation-Cl- cotransporters required for normal blood pressure homeostasis |
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| WNK4 regulates apical and basolateral Cl- flux in extrarenal epithelia |
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| WNK4 regulates the balance between renal NaCl reabsorption and K+ secretion |
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