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Results: 1-25 | 26-46
Results: 1-25/46
Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice
Authors: Scacheri, PC Crabtree, JS Novotny, EA Garrett-Beal, L Chen, A Edgemon, KA Marx, SJ Spiegel, AM Chandrasekharappa, SC Collins, FS
Citation: Pc. Scacheri et al., Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice, GENESIS, 30(4), 2001, pp. 259-263
Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns
Authors: Mohlke, KL Lange, EM Valle, TT Ghosh, S Magnuson, VL Silander, K Watanabe, RM Chines, PS Bergman, RN Tuomilehto, A Collins, FS Boehnke, M
Citation: Kl. Mohlke et al., Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns, GENOME RES, 11(7), 2001, pp. 1221-1226
Contemplating the end of the beginning
Authors: Collins, FS
Citation: Fs. Collins, Contemplating the end of the beginning, GENOME RES, 11(5), 2001, pp. 641-643
Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers
Authors: Lipkin, SM Wang, V Stoler, DL Anderson, GR Kirsch, I Hadley, D Lynch, HT Collins, FS
Citation: Sm. Lipkin et al., Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers, HUM MUTAT, 17(5), 2001, pp. 389-396
The tumor suppressor protein menin interacts with NF-kappa B proteins and inhibits NF-kappa B-mediated transactivation
Authors: Heppner, C Bilimoria, KY Agarwal, SK Kester, MB Whitty, LJ Guru, SC Chandrasekharappa, SC Collins, FS Spiegel, AM Marx, SJ Burns, AL
Citation: C. Heppner et al., The tumor suppressor protein menin interacts with NF-kappa B proteins and inhibits NF-kappa B-mediated transactivation, ONCOGENE, 20(36), 2001, pp. 4917-4925
Characterization of a MEN1 ortholog from Drosophila melanogaster
Authors: Guru, SC Prasad, NB Shin, EJ Hemavathy, K Lu, JN Ip, YT Agarwal, SK Marx, SJ Spiegel, AM Collins, FS Oliver, B Chandrasekharappa, SC
Citation: Sc. Guru et al., Characterization of a MEN1 ortholog from Drosophila melanogaster, GENE, 263(1-2), 2001, pp. 31-38
Genetics moves into the medical mainstream
Authors: Collins, FS Guttmacher, AE
Citation: Fs. Collins et Ae. Guttmacher, Genetics moves into the medical mainstream, J AM MED A, 286(18), 2001, pp. 2322-2324
Implications of the Human Genome Project for medical science
Authors: Collins, FS McKusick, VA
Citation: Fs. Collins et Va. Mckusick, Implications of the Human Genome Project for medical science, J AM MED A, 285(5), 2001, pp. 540-544
Translation of genomic research into health care - Reply
Authors: Collins, FS McKusick, VA
Citation: Fs. Collins et Va. Mckusick, Translation of genomic research into health care - Reply, J AM MED A, 285(19), 2001, pp. 2447-2448
A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors
Authors: Crabtree, JS Scacheri, PC Ward, JM Garrett-Beal, L Emmert-Buck, MR Edgemon, KA Lorang, D Libutti, SK Chandrasekharappa, SC Marx, SJ Spiegel, AM Collins, FS
Citation: Js. Crabtree et al., A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors, P NAS US, 98(3), 2001, pp. 1118-1123
The peroxisome poliferator-activated receptor-gamma 2 Pro12Ala variant - Association with type 2 diabetes and trait differences
Authors: Douglas, JA Erdos, MR Watanabe, RM Braun, A Johnston, CL Oeth, P Mohlke, KL Valle, TT Ehnholm, C Buchanan, TA Bergman, RN Collins, FS Boehnke, M Tuomilehto, J
Citation: Ja. Douglas et al., The peroxisome poliferator-activated receptor-gamma 2 Pro12Ala variant - Association with type 2 diabetes and trait differences, DIABETES, 50(4), 2001, pp. 886-890
The human genome project: Revealing the shared inheritance of all humankind
Authors: Collins, FS Mansoura, MK
Citation: Fs. Collins et Mk. Mansoura, The human genome project: Revealing the shared inheritance of all humankind, CANCER, 91(1), 2001, pp. 221-225
The human genome project: Revealing the shared inheritance of all humankind
Authors: Collins, FS Mansoura, MK
Citation: Fs. Collins et Mk. Mansoura, The human genome project: Revealing the shared inheritance of all humankind, CANC CYTOP, 91(1), 2001, pp. 221-225
Genetics resources on the Web (GROW)
Authors: Guttmacher, AE Collins, FS
Citation: Ae. Guttmacher et Fs. Collins, Genetics resources on the Web (GROW), GENET MED, 2(5), 2000, pp. 296-299
Of genes and genomes: What lies between the base pairs
Authors: Collins, FS Haseltine, WA
Citation: Fs. Collins et Wa. Haseltine, Of genes and genomes: What lies between the base pairs, J INVES MED, 48(5), 2000, pp. 295-301
MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability
Authors: Lipkin, SM Wang, V Jacoby, R Banerjee-Basu, S Baxevanis, AD Lynch, HT Elliott, RM Collins, FS
Citation: Sm. Lipkin et al., MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability, NAT GENET, 24(1), 2000, pp. 27-35
Oligonucleotide microarray based detection of repetitive sequence changes
Authors: Hacia, JG Edgemon, K Fang, N Mayer, RA Sudano, D Hunt, N Collins, FS
Citation: Jg. Hacia et al., Oligonucleotide microarray based detection of repetitive sequence changes, HUM MUTAT, 16(4), 2000, pp. 354-363
MENI gene mutation analysis of high-grade neuroendocrine lung carcinoma
Authors: Debelenko, LV Swalwell, JI Kelley, MJ Brambilla, E Manickam, P Baibakov, G Agarwal, SK Spiegel, AM Marx, SJ Chandrasekharappa, SC Collins, FS Travis, WD Emmert-Buck, MR
Citation: Lv. Debelenko et al., MENI gene mutation analysis of high-grade neuroendocrine lung carcinoma, GENE CHROM, 28(1), 2000, pp. 58-65
Identification and characterization of JunD missense mutants that lack menin binding
Authors: Knapp, JI Heppner, C Hickman, AB Burns, AL Chandrasekharappa, SC Collins, FS Marx, SJ Spiegel, AM Agarwal, SK
Citation: Ji. Knapp et al., Identification and characterization of JunD missense mutants that lack menin binding, ONCOGENE, 19(41), 2000, pp. 4706-4712
Isolation, characterization, expression and functional analysis of the zebrafish ortholog MEN1
Authors: Manickam, P Vogel, AM Agarwal, SK Oda, T Spiegel, AM Marx, SJ Collins, FS Weinstein, BM Chandrasekharappa, SC
Citation: P. Manickam et al., Isolation, characterization, expression and functional analysis of the zebrafish ortholog MEN1, MAMM GENOME, 11(6), 2000, pp. 448-454
Complete maternal isodisomy of chromosome 8 in an individual with an early-onset ileal carcinoid turner
Authors: Karanjawala, ZE Kaariainen, H Ghosh, S Tannenbaum, J Martin, C Ally, D Tuomilehto, J Valle, T Collins, FS
Citation: Ze. Karanjawala et al., Complete maternal isodisomy of chromosome 8 in an individual with an early-onset ileal carcinoid turner, AM J MED G, 93(3), 2000, pp. 207-210
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes
Authors: Ghosh, S Watanabe, RM Valle, TT Hauser, ER Magnuson, VL Langefeld, CD Ally, DS Mohlke, KL Silander, K Kohtamaki, K Chines, P Balow, J Birznieks, G Chang, J Eldridge, W Erdos, MR Karanjawala, ZE Knapp, JI Kudelko, K Martin, C Morales-Mena, A Musick, A Musick, T Pfahl, C Porter, R Rayman, JB Rha, D Segal, L Shapiro, S Sharaf, R Shurtleff, B So, A Tannenbaum, J Te, C Tovar, J Unni, A Welch, C Whiten, R Witt, A Blaschak-Harvan, J Douglas, JA Duren, WL Epstein, MP Fingerlin, TE Kaleta, HS Lange, EM Li, C McEachin, RC Stringham, HM Trager, E White, PP Eriksson, J Toivanen, L Vidgren, G Nylund, SJ Tuomilehto-Wolf, E Ross, EH Demirchyan, E Hagopian, WA Buchanan, TA Tuomilehto, J Bergman, RN Collins, FS Boehnke, M
Citation: S. Ghosh et al., The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes, AM J HU GEN, 67(5), 2000, pp. 1174-1185
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci
Authors: Watanabe, RM Ghosh, S Langefeld, CD Valle, TT Hauser, ER Magnuson, VL Mohlke, KL Silander, K Ally, DS Chines, P Blaschak-Harvan, J Douglas, JA Duren, WL Epstein, MP Fingerlin, TE Kaleta, HS Lange, EM Li, C McEachin, RC Stringham, HM Trager, E White, PP Balow, J Birznieks, G Chang, J Eldridge, W Erdos, MR Karanjawala, ZE Knapp, JI Kudelko, K Martin, C Morales-Mena, A Musick, A Musick, T Pfahl, C Porter, R Rayman, JB Rha, D Segal, L Shapiro, S Sharaf, R Shurtleff, B So, A Tannenbaum, J Te, C Tovar, J Unni, A Welch, C Whiten, R Witt, A Kohtamaki, K Ehnholm, C Eriksson, J Toivanen, L Vidgren, G Nylund, SJ Tuomilehto-Wolf, E Ross, EH Demirchyan, E Hagopian, WA Buchanan, TA Tuomilehto, J Bergman, RN Collins, FS Boehnke, M
Citation: Rm. Watanabe et al., The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci, AM J HU GEN, 67(5), 2000, pp. 1186-1200
The gene for multiple endocrine neoplasia type 1: Recent findings
Authors: Marx, SJ Agarwal, SK Heppner, C Kim, YS Kester, MB Goldsmith, PK Skarulis, MC Spiegel, AM Burns, AL Debelenko, LV Zhuang, Z Lubensky, IA Liotta, LA Emmert-Buck, MR Guru, SC Manickam, P Crabtree, JS Collins, FS Chandrasekharappa, SC
Citation: Sj. Marx et al., The gene for multiple endocrine neoplasia type 1: Recent findings, BONE, 25(1), 1999, pp. 119-122
A DNA polymorphism discovery resource for research on human genetic variation (vol 8, pg 1229, 1998)
Authors: Collins, FS Brooks, LD Chakravarti, A
Citation: Fs. Collins et al., A DNA polymorphism discovery resource for research on human genetic variation (vol 8, pg 1229, 1998), GENOME RES, 9(2), 1999, pp. 210-210
Risultati: 1-25 | 26-46