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F-Spondin, expressed in somite regions avoided by neural crest cells, mediates inhibition of distinct somite domains to neural crest migration.
Debby-Brafman A, Burstyn-Cohen T, Klar A, Kalcheim C. Debby-Brafman A, et al. Among authors: klar a. Neuron. 1999 Mar;22(3):475-88. doi: 10.1016/s0896-6273(00)80703-5. Neuron. 1999. PMID: 10197528
Plasmin-mediated release of the guidance molecule F-spondin from the extracellular matrix.
Tzarfaty-Majar V, López-Alemany R, Feinstein Y, Gombau L, Goldshmidt O, Soriano E, Muñoz-Cánoves P, Klar A. Tzarfaty-Majar V, et al. Among authors: klar a. J Biol Chem. 2001 Jul 27;276(30):28233-41. doi: 10.1074/jbc.M102585200. Epub 2001 May 18. J Biol Chem. 2001. PMID: 11359777
F-spondin is a contact-repellent molecule for embryonic motor neurons.
Tzarfati-Majar V, Burstyn-Cohen T, Klar A. Tzarfati-Majar V, et al. Among authors: klar a. Proc Natl Acad Sci U S A. 2001 Apr 10;98(8):4722-7. doi: 10.1073/pnas.081062398. Epub 2001 Apr 3. Proc Natl Acad Sci U S A. 2001. PMID: 11287656 Free PMC article.
F-spondin and mindin: two structurally and functionally related genes expressed in the hippocampus that promote outgrowth of embryonic hippocampal neurons.
Feinstein Y, Borrell V, Garcia C, Burstyn-Cohen T, Tzarfaty V, Frumkin A, Nose A, Okamoto H, Higashijima S, Soriano E, Klar A. Feinstein Y, et al. Among authors: klar a. Development. 1999 Aug;126(16):3637-48. Development. 1999. PMID: 10409509
F-Spondin is required for accurate pathfinding of commissural axons at the floor plate.
Burstyn-Cohen T, Tzarfaty V, Frumkin A, Feinstein Y, Stoeckli E, Klar A. Burstyn-Cohen T, et al. Among authors: klar a. Neuron. 1999 Jun;23(2):233-46. doi: 10.1016/s0896-6273(00)80776-x. Neuron. 1999. PMID: 10399931
Accumulation of F-spondin in injured peripheral nerve promotes the outgrowth of sensory axons.
Burstyn-Cohen T, Frumkin A, Xu YT, Scherer SS, Klar A. Burstyn-Cohen T, et al. Among authors: klar a. J Neurosci. 1998 Nov 1;18(21):8875-85. doi: 10.1523/JNEUROSCI.18-21-08875.1998. J Neurosci. 1998. PMID: 9786993 Free PMC article.
A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency.
Lasry I, Seo YA, Ityel H, Shalva N, Pode-Shakked B, Glaser F, Berman B, Berezovsky I, Goncearenco A, Klar A, Levy J, Anikster Y, Kelleher SL, Assaraf YG. Lasry I, et al. Among authors: klar a. J Biol Chem. 2012 Aug 24;287(35):29348-61. doi: 10.1074/jbc.M112.368159. Epub 2012 Jun 25. J Biol Chem. 2012. PMID: 22733820 Free PMC article. Clinical Trial.
Mitochondrial myopathy, Fanconi syndrome with impaired glycogen and galactose metabolism.
Hurvitz H, Kerem E, Elpeleg ON, Barash V, Klar A, Mor C, Branski D. Hurvitz H, et al. Among authors: klar a. Prog Clin Biol Res. 1989;306:143-8. Prog Clin Biol Res. 1989. PMID: 2740408 No abstract available.
Mapping replication units in animal cells.
Handeli S, Klar A, Meuth M, Cedar H. Handeli S, et al. Among authors: klar a. Cell. 1989 Jun 16;57(6):909-20. doi: 10.1016/0092-8674(89)90329-2. Cell. 1989. PMID: 2544294
Muscular carnitine palmitoyltransferase II deficiency in infancy.
Hurvitz H, Klar A, Korn-Lubetzki I, Wanders RJ, Elpeleg ON. Hurvitz H, et al. Among authors: klar a. Pediatr Neurol. 2000 Feb;22(2):148-50. doi: 10.1016/s0887-8994(99)00125-3. Pediatr Neurol. 2000. PMID: 10738923
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