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Results 1 - 10 of 162 for Rp -cAMPS
  1. Retinitis pigmentosa 
    ... other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing Registry: Retinitis pigmentosa Cone ... for Rare Disorders (NORD) ClinicalTrials.gov RETINITIS PIGMENTOSA; RP PubMed Daiger SP, Bowne SJ, Sullivan LS. Perspective ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  2. Liddle syndrome 
    ... Y, Canessa C, Iwasaki T, Rossier B, Lifton RP. Hypertension caused by a truncated epithelial sodium channel ... Shimkets R, Nelson-Williams C, Rossier BC, Lifton RP. A de novo missense mutation of the beta ...
    https://medlineplus.gov/genetics/condition/liddle-syndrome - Genetics
  3. Aldosterone-producing adenoma 
    ... G, Akerstrom G, Wang W, Carling T, Lifton RP. K+ channel mutations in adrenal aldosterone-producing adenomas ... P, Carling T, Fahlke C, Hidalgo P, Lifton RP. Somatic and germline CACNA1D calcium channel mutations in ...
    https://medlineplus.gov/.../condition/aldosterone-producing-adenoma - Genetics
  4. JAG1 gene 
    ... Epub 2007 Aug 24. Citation on PubMed Colliton RP, Bason L, Lu FM, Piccoli DA, Krantz ID, ... 45902.69. Citation on PubMed Morrissette JD, Colliton RP, Spinner NB. Defective intracellular transport and processing of ...
    https://medlineplus.gov/genetics/gene/jag1 - Genetics
  5. Pseudohypoaldosteronism type 2 
    ... HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP. Mutations in kelch-like 3 and cullin 3 ... H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. Human hypertension caused by mutations in WNK kinases. ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
  6. WNK4 gene 
    ... MD, Volkman HM, Wilson FH, Hebert SC, Lifton RP. WNK4 regulates activity of the epithelial Na+ channel ... H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. Human hypertension caused by mutations in WNK kinases. ...
    https://medlineplus.gov/genetics/gene/wnk4 - Genetics
  7. Nearsightedness 
    ... Myopia; Burdon KP, Craig JE, Iyengar SK, Igo RP Jr, Lass JH Jr; Fuchs' Genetics Multi-Center ... Biino G, Concas MP, Schwantes-An TH, Igo RP Jr, Cuellar-Partida G, Martin NG, Craig JE, ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  8. KCNJ5 gene 
    ... G, Akerstrom G, Wang W, Carling T, Lifton RP. K+ channel mutations in adrenal aldosterone-producing adenomas ... Dec 27. Citation on PubMed Scholl UI, Lifton RP. New insights into aldosterone-producing adenomas and hereditary ...
    https://medlineplus.gov/genetics/gene/kcnj5 - Genetics
  9. SLC12A3 gene 
    ... A, Finberg K, Burleson L, Gill JR, Lifton RP. Mutations in the Na-Cl cotransporter reduce blood ... Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes ...
    https://medlineplus.gov/genetics/gene/slc12a3 - Genetics
  10. X-linked infantile nystagmus 
    ... S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, ... M, Kumar AS, Farooq SJ, Degg C, Gale RP, Reinecke RD, Woodruff G, Langmann A, Lindner S, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
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