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5. Imprinted cell memory in glycogen storage disorder 1a

8. The Ammiad experiment

14. Abstracts of papers presented at the 15th conference of the weed science society of Israel

15. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling

19. Genome size in natural and synthetic autopolyploids and in a natural segmental allopolyploid of several Triticeae species

21. Nuclear DNA amount and genome downsizing in natural and synthetic allopolyploids of the genera Aegilops and Triticum

25. Genome size and genome evolution in diploid Triticeae species

30. Abstracts of Presentations at the 19th Congress of the Israeli Phytopathological Society: February 16–17, 1998 ARO, the Volcani Center, Bet Dagan, Israel

32. The 18th congress of the israeli phytopathological society: February 3-4, 1997

35. Abstracts of papers presented at the 8th conference of the Entomological Society of Israel Abstracts of papers presented at the 17th congress of the Israeli Phytopathological Society: January 18, 1996 ARO, The Volcani Center, Bet Dagan, Israel February 19–20, 1996 ARO, The Volcani Center, Bet Dagan, Israel

36. Abstracts of papers presented at the 16th Congress of the Israeli Phytopathological Society: February 20–21, 1995 ARO, The Volcani Center, Bet Dagan, Israel

41. DNAJC12: A molecular chaperone involved in proteostasis, PKU, biogenic amines metabolism and beyond?

43. Clinically Distinct Phenotypes of Canavan Disease Correlate with Residual Aspartoacylase Enzyme Activity

44. A novel inborn error of the Coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-Methyltransferase deficiency

46. Endemic and panglobal genetic groups, and divergence of host-associated forms in worldwide collections of the wheat leaf rust fungus Puccinia triticinaas determined by genotyping by sequencing

47. Evidence that rab27a mutations are associated with neurological involvement, not simply the hemophagocytic syndrome, in patients with Griscelli syndrome

48. Mutations in a novel gene, SUTAL, cause a unique form of Hermansky-Pudlak syndrome, HPS-3

50. The CTNS promter and its mutations causing cystinosis

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