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Results:
1-9
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Results: 9
Authors:
Mandel, H
Szargel, R
Labay, V
Elpeleg, O
Saada, A
Shalata, A
Anbinder, Y
Berkowitz, D
Hartman, C
Barak, M
Eriksson, S
Cohen, N
Citation: H. Mandel et al., The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA (vol 29, pg 337, 2001), NAT GENET, 29(4), 2001, pp. 491-491
Authors:
Mandel, H
Szargel, R
Labay, V
Elpeleg, O
Saada, A
Shalata, A
Anbinder, Y
Berkowitz, D
Hartman, C
Barak, M
Eriksson, S
Cohen, N
Citation: H. Mandel et al., The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA, NAT GENET, 29(3), 2001, pp. 337-341
Authors:
Sprecher, E
Bergman, R
Richard, G
Lurie, R
Shalev, S
Petronius, D
Shalata, A
Anbinder, Y
Leibu, R
Perlman, I
Cohen, N
Szargel, R
Citation: E. Sprecher et al., Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin, NAT GENET, 29(2), 2001, pp. 134-136
Authors:
Shalata, A
Mittova, V
Volokita, M
Guy, M
Tal, M
Citation: A. Shalata et al., Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: The root antioxidative system, PHYSL PLANT, 112(4), 2001, pp. 487-494
Authors:
Shalata, A
Neumann, PM
Citation: A. Shalata et Pm. Neumann, Exogenous ascorbic acid (vitamin C) increases resistance to salt stress and reduces lipid peroxidation, J EXP BOT, 52(364), 2001, pp. 2207-2211
Authors:
Naveh, Y
Shalata, A
Shenker, L
Coleman, R
Citation: Y. Naveh et al., Absorption of iron in rats with experimental enteritis, BIOMETALS, 13(1), 2000, pp. 29-35
Authors:
Shalata, A
Mandel, H
Dorche, C
Zabot, MT
Shalev, S
Hugeirat, Y
Arieh, D
Ronit, Z
Reiss, J
Anbinder, Y
Cohen, N
Citation: A. Shalata et al., Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in Northern Israel using polymorphic DNA markers, PRENAT DIAG, 20(1), 2000, pp. 7-11
Authors:
Sprecher, E
Shalata, A
Dabhah, K
Futerman, B
Lin, S
Szargel, R
Bergman, R
Friedman-Birnbaum, R
Cohen, N
Citation: E. Sprecher et al., Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene, J AM ACAD D, 42(6), 2000, pp. 978-982
Authors:
Labay, V
Raz, T
Baron, D
Mandel, H
Williams, H
Barrett, T
Szargel, R
McDonald, L
Shalata, A
Nosaka, K
Gregory, S
Cohen, N
Citation: V. Labay et al., Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness, NAT GENET, 22(3), 1999, pp. 300-304
Risultati:
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