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Results: 1-17 |
Results: 17
The Bsml vitamin D receptor gene polymorphism in Israeli populations and in perimenopausal and osteoporotic Ashkenazi women
Authors: Pollak, RD Blumenfeld, A Bejarano-Achache, I Idelson, M Hochner, DC
Citation: Rd. Pollak et al., The Bsml vitamin D receptor gene polymorphism in Israeli populations and in perimenopausal and osteoporotic Ashkenazi women, AM J NEPHR, 21(3), 2001, pp. 185-188
An improved procedure for the lateral lithiation of ethyl 4-acetyl-5-methyl-3-isoxazolyl carboxylate
Authors: Burkhart, DJ Zhou, PW Blumenfeld, A Twamley, B Natale, NR
Citation: Dj. Burkhart et al., An improved procedure for the lateral lithiation of ethyl 4-acetyl-5-methyl-3-isoxazolyl carboxylate, TETRAHEDRON, 57(38), 2001, pp. 8041-8048
Interferon beta-1 a for optic neuritis patients at high risk for multiple sclerosis
Authors: O'Connor, P Fleming, P Gray, T Jacobs, L Miller, C Munschauer, F Kinkel, RP Bolibrush, D Cohen, J Freedman, M Webb, U Rabinowicz, H Metz, LM Patry, D Yeung, M Peters, S Hashimoto, S Morrison, W Oger, J Panitch, H Costello, K Bever, C Stuart, W Court, D Stuart, D Tornatore, C Bartlett, D Richert, J Duquette, P Dubois, R Bernier, G Scott, T Pappert, L Brillman, J Felton, W Anderson, T Astruc, J Rose, J Kline, J Burns, J Murray, T Weldon, P Bhan, V Maxner, CE Wall, M Vining, L Grabowski, T Apatoff, B Arapello, K Friedman, J Galetta, S Pfohl, D Liu, G Rice, G Bental, T Mandalfino, P Eggenberger, E Snider, D Kaufman, D Guarnaccia, J Shepard, M Goldstein, J Reiss, M Carter, E Glista, G Rolak, L Scheller, L Jacobson, D Warner, J Goodman, A Petrie, M Mattson, D Karlin, K Wallin, A Stefoski, D Brod, S Cerretta, E Wolinsky, J Arnold, D Arnoutelis, R Durcan, L Kupersmith, M Cappolino, L Herbert, J Rosenberg, J McHugh, D Blumenfeld, A Smith, C Kuder, D Hamilton, S Thurston, S McGee, J O'Bannon, J Kaufman, M Butler, M Putnam, S Rammohan, K Siffort, A Lynn, J Selhorst, J Holzemer, E Hayat, G Tselis, A Coon, C Lisak, R Wray, S Sexton, P Lehrich, J Cook, S Jotkowitz, A Bansil, S Newman, N Brown, J Pennell, P Gilmore, J Carter, J Buckner, J Caselli, R Kerson, L Camasso, M Donneief, G Cooper, J Richardson, B Kung, C Goodwin, J Johnson, T Gulati, A Hedges, T Yardley, C Tran, T Brown, W Ehrenberg, B Horowitz, S Bonnett, A Burger, R Javerbaum, J Griffin, C Whaley, RJ Jeffery, D Jackson, SE Bastings, E Kasper, L Ryan, K Bernat, J Mass, M Hanel, SC Bourdette, D Guy, J Wilson, M Greer, M Lucchinetti, C Botten, M Noseworthy, J Walker, A Muntz, B Tyor, W Simon, J Meyer, M Leek, R Gustafson, C Singel, D Quandt, B Miller, DE Coombs, B Cajade-Law, A Lajaunie, M Escott, E Miller, A Richert, J Cohen, J Vollmer, T Oger, J Jacobs, L Beck, R Kinkel, RP Brownscheidle, C Murray, TJ Simon, J Antel, J Myers, L Birnbaum, G Reingold, S Burde, R Sibley, W Ware, J Blanchard, N Lloyd, K Park, H Sandrock, A Simonian, N Slasor, P Votruba, F White, K Beck, R Chandler, DL Cole, S Felton, W Galetta, S Jacobs, L Kinkel, RP Kupersmith, M Murray, TJ Newman, N Sandrock, A Simon, J Simonian, N
Citation: P. O'Connor et al., Interferon beta-1 a for optic neuritis patients at high risk for multiple sclerosis, AM J OPHTH, 132(4), 2001, pp. 463-471
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia
Authors: Slaugenhaupt, SA Blumenfeld, A Gill, SP Leyne, M Mull, J Cuajungco, MP Liebert, CB Chadwick, B Idelson, M Reznik, L Robbins, CM Makalowska, I Brownstein, MJ Krappmann, D Scheidereit, C Maayan, C Axelrod, FB Gusella, JF
Citation: Sa. Slaugenhaupt et al., Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia, AM J HU GEN, 68(3), 2001, pp. 598-605
Traumatic adrenal injury in children
Authors: Schwarz, M Horev, G Freud, E Ziv, N Blumenfeld, A Steinberg, R Kornreich, L
Citation: M. Schwarz et al., Traumatic adrenal injury in children, ISR MED ASS, 2(2), 2000, pp. 132-134
Ethnic differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Israeli populations
Authors: Pollak, RD Friedlander, Y Pollak, A Idelson, M Bejarano-Achache, I Blumenfeld, A
Citation: Rd. Pollak et al., Ethnic differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Israeli populations, GENET TEST, 4(3), 2000, pp. 309-311
Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31
Authors: Chadwick, BP Leyne, M Gill, S Liebert, CB Mull, J Mezey, E Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, M Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31, MAMM GENOME, 11(1), 2000, pp. 81-83
Infrared and NMR spectroscopic studies of n-alkanethiols chemically grafted on dimethylzinc-modified silica surfaces
Authors: Boiadjiev, V Blumenfeld, A Gutow, J Tysoe, WT
Citation: V. Boiadjiev et al., Infrared and NMR spectroscopic studies of n-alkanethiols chemically grafted on dimethylzinc-modified silica surfaces, CHEM MATER, 12(9), 2000, pp. 2604-2613
A simple method of intraoperative confirmation of intestinal patency
Authors: Steinberg, R Freud, E Simhi, E Blumenfeld, A Zer, M
Citation: R. Steinberg et al., A simple method of intraoperative confirmation of intestinal patency, PEDIAT SURG, 16(7), 2000, pp. 538-539
Bone mineral metabolism in adults with beta-thalassaemia major and intermedia
Authors: Pollak, RD Rachmilewitz, E Blumenfeld, A Idelson, M Goldfarb, AW
Citation: Rd. Pollak et al., Bone mineral metabolism in adults with beta-thalassaemia major and intermedia, BR J HAEM, 111(3), 2000, pp. 902-907
The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) geneand vascular dementia
Authors: Pollak, RD Pollak, A Idelson, M Bejarano-Achache, I Doron, D Blumenfeld, A
Citation: Rd. Pollak et al., The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) geneand vascular dementia, J AM GER SO, 48(6), 2000, pp. 664-668
Prenatal diagnosis of oculocutaneous albinism type I: Review and personal experience
Authors: Rosenmann, E Rosenmann, A Ne'eman, Z Lewin, A Bejarano-Achache, I Blumenfeld, A
Citation: E. Rosenmann et al., Prenatal diagnosis of oculocutaneous albinism type I: Review and personal experience, PEDIATR D P, 2(5), 1999, pp. 404-414
On the reaction pathway for the formation of benzene from acetylene catalyzed by palladium
Authors: Kaltchev, M Stacchiola, D Molero, H Wu, G Blumenfeld, A Tysoe, WT
Citation: M. Kaltchev et al., On the reaction pathway for the formation of benzene from acetylene catalyzed by palladium, CATAL LETT, 60(1-2), 1999, pp. 11-14
Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31
Authors: Chadwick, BP Mull, J Helbling, LA Gill, S Leyne, M Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, N Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31, GENOMICS, 58(3), 1999, pp. 302-309
Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene
Authors: Chadwick, BP Gill, S Leyne, M Mull, J Liebert, CB Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, M Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene, GENE, 240(1), 1999, pp. 67-73
Ovarian masses in children
Authors: Freud, E Golinsky, D Steinberg, RM Blumenfeld, A Yaniv, I Zer, M
Citation: E. Freud et al., Ovarian masses in children, CLIN PEDIAT, 38(10), 1999, pp. 573-577
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31
Authors: Blumenfeld, A Slaugenhaupt, SA Liebert, CB Temper, V Maayan, C Gill, S Lucente, DE Idelson, M MacCormack, K Monahan, MA Mull, J Leyne, M Mendillo, M Schiripo, T Mishori, E Breakefield, X Axelrod, FB Gusella, JF
Citation: A. Blumenfeld et al., Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31, AM J HU GEN, 64(4), 1999, pp. 1110-1118
Risultati: 1-17 |