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:
Hebert, JR
Peterson, KE
Hurley, TG
Stoddard, AM
Cohen, N
Field, AE
Sorensen, G
Citation: Jr. Hebert et al., The effect of social desirability trait on self-reported dietary measures among multi-ethnic female health center employees, ANN EPIDEMI, 11(6), 2001, pp. 417-427
Authors:
Cohen, N
Betts, DR
Trakhtenbrot, L
Niggli, FK
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Brok-Simoni, F
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Meitar, D
Citation: N. Cohen et al., Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY), GENE CHROM, 31(3), 2001, pp. 201-208
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Cohen, N
Sharma, M
Kentsis, A
Perez, JM
Strudwick, S
Borden, KLB
Citation: N. Cohen et al., PML RING suppresses oncogenic transformation by reducing the affinity of eIF4E for mRNA, EMBO J, 20(16), 2001, pp. 4547-4559
Citation: N. Cohen et Pm. Wassarman, Association of egg zone pellucida glycoprotein mZP3 with sperm protein sp56 during fertilization in mice, INT J DEV B, 45(3), 2001, pp. 569-576
Authors:
Gorelik, O
Almoznino-Sarafian, D
Alon, I
Rapoport, MJ
Goltsman, G
Herbert, M
Modai, D
Cohen, N
Citation: O. Gorelik et al., Acute inflammatory myopathy with severe subcutaneous edema, a new variant?Report of two cases and review of the literature, RHEUM INTL, 20(4), 2001, pp. 163-166
Authors:
Cohen, N
Rozenfeld-Granot, G
Hardan, I
Brok-Simoni, F
Amariglio, N
Rechavi, G
Trakhtenbrot, L
Citation: N. Cohen et al., Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis, CANC GENET, 128(2), 2001, pp. 114-119
Authors:
Cohen, N
Almoznino-Sarafian, D
Alon, I
Gorelik, O
Koopfer, M
Chachashvily, S
Shteinshnaider, M
Litvinjuk, V
Modai, D
Citation: N. Cohen et al., Adequacy of anticoagulation in patients with atrial fibrillation: Effect of various parameters, CLIN CARD, 24(5), 2001, pp. 380-384
Authors:
Averbukh, Z
Modai, D
Sandbank, J
Berman, S
Cohn, M
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Cohen, N
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Weissgarten, J
Citation: Z. Averbukh et al., Red eye syndrome: Clinical and experimental experience in a new aspect of diffuse eosinophilic infiltration?, ARTIF ORGAN, 25(6), 2001, pp. 437-440
Authors:
Siegel, C
Laska, E
Haugland, G
O'Neill, D
Cohen, N
Lesser, M
Citation: C. Siegel et al., The construction of community indexes of mental health and social and mental well-being and their application to New York City (vol 23, pg 315, 2000), EVAL PROG P, 24(4), 2001, pp. 451-451
Authors:
Parasol, N
Cohen, N
Zemishlany, Z
Lerer, B
Kosower, NS
Citation: N. Parasol et al., Duffy antigen/receptor for chemokines (DARC): Genotypes in Ashkenazi and non-Ashkenazi Jews in Israel, HUMAN BIOL, 73(2), 2001, pp. 307-313
Authors:
Rusch, L
Oakley, J
Miller, F
Speidel, R
Barnett, R
Gabriel, H
Scott, R
Hillebrand, G
Cohen, N
Silber, N
Feinman, J
Hellman, D
Braucher, J
Neff, S
Citation: L. Rusch et al., Questions and answers, HAST LAW J, 52(3), 2001, pp. 691-701
Authors:
Robert, J
Menoret, A
Basu, S
Cohen, N
Srivastava, PK
Citation: J. Robert et al., Phylogenetic conservation of the molecular and immunological properties ofthe chaperones gp96 and hsp70, EUR J IMMUN, 31(1), 2001, pp. 186-195
Authors:
Raz, T
Labay, V
Baron, D
Szargel, R
Anbinder, Y
Barrett, T
Rabl, W
Viana, MB
Mandel, H
Baruchel, A
Cayuela, JM
Cohen, N
Citation: T. Raz et al., The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families, HUM MUTAT, 16(1), 2000, pp. 37-42