Tamara Potikha
Affiliations: | 1993-1997 | Plant Sciences | Institute of Life Sciences, The Hebrew University of Jerusalem |
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"Tamara Potikha"Parents
Sign in to add mentor| Deborah P. Delmer | post-doc | 1993-1997 | Institute of Life Sciences, The Hebrew University of Jerusalem |
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| Horev L, Tosti A, Rosen I, et al. (2009) Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair. Journal of the American Academy of Dermatology. 61: 813-8 |
| Horev L, Potikha T, Ayalon S, et al. (2005) A novel splice-site mutation in ECM-1 gene in a consanguineous family with lipoid proteinosis. Experimental Dermatology. 14: 891-7 |
| Potikha T, Kassem S, Haber EP, et al. (2005) p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas. Laboratory Investigation; a Journal of Technical Methods and Pathology. 85: 364-75 |
| Tornovsky S, Crane A, Cosgrove KE, et al. (2004) Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity. The Journal of Clinical Endocrinology and Metabolism. 89: 6224-34 |
| Hinderlich S, Salama I, Eisenberg I, et al. (2004) The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy. Febs Letters. 566: 105-9 |
| Eisenberg I, Avidan N, Potikha T, et al. (2001) The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nature Genetics. 29: 83-7 |
| Potikha T, Delmer DP. (1995) A mutant of Arabidopsis thaliana displaying altered patterns of cellulose deposition The Plant Journal. 7: 453-460 |