Resultados de procura - Karthikeyan Radhakrishnan
- Mostrando 1 - 7 Resultados de 7
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Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification por Lars Schlotawa, Laura Adang, Karthikeyan Radhakrishnan, Rebecca C. Ahrens‐Nicklas
Publicado 2020Revisão -
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Comparative Evaluation of pH and In Vitro Cytotoxicity of Zinc Oxide–Ozonated Eugenol and Conventional Zinc Oxide Eugenol as Endodontic Sealers por Ravivarman, Chandramohan, Jeyasenthil, Athikesavan, Ajay, Ranganathan, Nilofernisha, Nasir, Karthikeyan, Radhakrishnan, Rajkumar, Durairaj
Publicado 2020Text -
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4
Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann–Pick C1 disease — Lysosomal storage disorders caused by defects of non-lysosomal proteins por Thomas Dierks, Lars Schlotawa, Marc‐André Frese, Karthikeyan Radhakrishnan, Kurt Von Figura, Bernhard Schmidt
Publicado 2008Revisão -
5
Effect of Green Tea Extract Mouthrinse and Probiotic Mouthrinse on Salivary pH in a Group of Schoolchildren: An In Vivo Study por Manikandan, Saranya, Behera, Subasish, Karthikeyan, Radhakrishnan, Niranjana, Arumugasamy, Bharathan, Rajendran, Mohammed, Omar Farooq Burhanuddin
Publicado 2020Text -
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SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency por Lars Schlotawa, Eva C. Ennemann, Karthikeyan Radhakrishnan, Bernhard Schmidt, Anupam Chakrapani, H.‐J. Christen, Hugo W. Moser, Beat Steinmann, Thomas Dierks, Jutta Gärtner
Publicado 2011Artigo -
7
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease por Laura Adang, Lars Schlotawa, Samuel Groeschel, Christiane Kehrer, K. Harzer, Orna Staretz‐Chacham, Thiago Oliveira Silva, Ida Vanessa Döederlein Schwartz, Jutta Gärtner, Mauricio De Castro, Carrie Costin, Esperanza Font–Montgomery, Thomas Dierks, Karthikeyan Radhakrishnan, Rebecca C. Ahrens‐Nicklas
Publicado 2020Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Gene
Biochemistry
Chemistry
Disease
Enzyme
Medicine
Phenotype
Sulfatase
Cell biology
Internal medicine
Lysosomal storage disease
Pathology
Age of onset
Biogenesis
Cathepsin D
Cell
Cholesterol
Compound heterozygosity
Endosome
Enzyme replacement therapy
Genetics
Genotype
Golgi apparatus
Hurler syndrome
Intracellular
Leukodystrophy
Lysosome
Mannose 6-phosphate receptor
Metachromatic leukodystrophy