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Results: 1-21 |
Results: 21
Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva
Authors: Nucci, MR Weremowicz, S Neskey, DM Sornberger, K Tallini, G Morton, CC Quade, BJ
Citation: Mr. Nucci et al., Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva, GENE CHROM, 32(2), 2001, pp. 172-176
STK25 is a candidate gene for pseudopseudohypoparathyroidism
Authors: Davids, MS Crawford, E Weremowicz, S Morton, CC Copeland, NG Gilbert, DJ Jenkins, NA Phelan, MC Comb, MJ Melnick, MB
Citation: Ms. Davids et al., STK25 is a candidate gene for pseudopseudohypoparathyroidism, GENOMICS, 77(1-2), 2001, pp. 2-4
Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases
Authors: Weremowicz, S Sandstrom, DJ Morton, CC Niedzwiecki, CA Sandstrom, MM Bieber, FR
Citation: S. Weremowicz et al., Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases, PRENAT DIAG, 21(4), 2001, pp. 262-269
Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57(KIP2)
Authors: Castrillon, DH Sun, DQ Weremowicz, S Fisher, RA Crum, CP Genest, DR
Citation: Dh. Castrillon et al., Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57(KIP2), AM J SURG P, 25(10), 2001, pp. 1225-1230
Mutations in the protein kinase A Rl alpha regulatory subunit cause familial cardiac myxomas and Carney complex (vol 106, pg R31, 2000)
Authors: Casey, M Vaughan, CJ He, J Hatcher, CJ Winter, JM Weremowicz, S Montgomery, K Kucherlapati, R Morton, CC Basson, CT
Citation: M. Casey et al., Mutations in the protein kinase A Rl alpha regulatory subunit cause familial cardiac myxomas and Carney complex (vol 106, pg R31, 2000), J CLIN INV, 107(2), 2001, pp. 235-235
A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis
Authors: Vaughan, CJ Weremowicz, S Goldstein, MM Casey, M Hart, M Hahn, RT Devereux, RB Girardi, L Schoen, FJ Fletcher, JA Morton, CC Basson, CT
Citation: Cj. Vaughan et al., A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis, GENE CHROM, 28(2), 2000, pp. 133-137
Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14
Authors: Pedeutour, F Quade, BJ Sornberger, K Tallini, G Ligon, AH Weremowicz, S Morton, CC
Citation: F. Pedeutour et al., Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14, GENE CHROM, 27(2), 2000, pp. 209-215
SMARCAD1, a novel human helicase family-defining member associated with genetic instability: Cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases
Authors: Adra, CN Donato, JL Badovinac, R Syed, F Kheraj, R Cai, HB Moran, C Kolker, MT Turner, H Weremowicz, S Shirakawa, T Morton, CC Schnipper, LE Drews, R
Citation: Cn. Adra et al., SMARCAD1, a novel human helicase family-defining member associated with genetic instability: Cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases, GENOMICS, 69(2), 2000, pp. 162-173
A novel conserved cochlear gene, OTOR: Identification, expression analysis, and chromosomal mapping
Authors: Robertson, NG Heller, S Lin, JS Resendes, BL Weremowicz, S Denis, CS Bell, AM Hudspeth, AJ Morton, CC
Citation: Ng. Robertson et al., A novel conserved cochlear gene, OTOR: Identification, expression analysis, and chromosomal mapping, GENOMICS, 66(3), 2000, pp. 242-248
Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: Sequence, expression, alternative splicing, and chromosomal localization
Authors: Guo, L Schreiber, TH Weremowicz, S Morton, CC Lee, C Zhou, J
Citation: L. Guo et al., Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: Sequence, expression, alternative splicing, and chromosomal localization, GENOMICS, 64(3), 2000, pp. 241-251
Mutations in the protein kinase A R1 alpha regulatory subunit cause familial cardiac myxomas and Carney complex
Authors: Casey, M Vaughan, CJ He, J Hatcher, CJ Winter, JM Weremowicz, S Montgomery, K Kucherlapati, R Morton, CC Basson, CT
Citation: M. Casey et al., Mutations in the protein kinase A R1 alpha regulatory subunit cause familial cardiac myxomas and Carney complex, J CLIN INV, 106(5), 2000, pp. R31-R38
Human calcium transport protein CaT1
Authors: Peng, JB Chen, XZ Berger, UV Weremowicz, S Morton, CC Vassilev, PM Brown, EM Hediger, MA
Citation: Jb. Peng et al., Human calcium transport protein CaT1, BIOC BIOP R, 278(2), 2000, pp. 326-332
Human vitamin C (L-ascorbic acid) transporter SVCT1
Authors: Wang, YX Mackenzie, B Tsukaguchi, H Weremowicz, S Morton, CC Hediger, MA
Citation: Yx. Wang et al., Human vitamin C (L-ascorbic acid) transporter SVCT1, BIOC BIOP R, 267(2), 2000, pp. 488-494
Primary parauterine leiomyoma with a t(6;14)
Authors: Dal Cin, P Quade, BJ Weremowicz, S Morton, CC Pauwels, P Van den Berghe, H
Citation: P. Dal Cin et al., Primary parauterine leiomyoma with a t(6;14), GENE CHROM, 26(4), 1999, pp. 383-384
Is HMGIC rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas?
Authors: Weremowicz, S Morton, CC
Citation: S. Weremowicz et Cc. Morton, Is HMGIC rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas?, GENE CHROM, 24(2), 1999, pp. 172-173
The thrombospondin-4 gene
Authors: Newton, G Weremowicz, S Morton, CC Jenkins, NA Gilbert, DJ Copeland, NG Lawler, J
Citation: G. Newton et al., The thrombospondin-4 gene, MAMM GENOME, 10(10), 1999, pp. 1010-1016
Functional and molecular characterization of the human neutral solute channel aquaporin-9
Authors: Tsukaguchi, H Weremowicz, S Morton, CC Hediger, MA
Citation: H. Tsukaguchi et al., Functional and molecular characterization of the human neutral solute channel aquaporin-9, AM J P-REN, 277(5), 1999, pp. F685-F696
Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6
Authors: Sornberger, KS Weremowicz, S Williams, AJ Quade, BJ Ligon, AH Pedeutour, F Vanni, R Morton, CC
Citation: Ks. Sornberger et al., Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6, CANC GENET, 114(1), 1999, pp. 9-16
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations
Authors: Basson, CT Huang, TS Lin, RC Bachinsky, DR Weremowicz, S Vaglio, A Bruzzone, R Quadrelli, R Lerone, M Romeo, G Silengo, M Pereira, A Krieger, J Mesquita, SF Kamisago, M Morton, CC Pierpont, MEM Muller, CW Seidman, JG Seidman, CE
Citation: Ct. Basson et al., Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations, P NAS US, 96(6), 1999, pp. 2919-2924
Balanced translocation of 10q and 13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome
Authors: Ahmed, SF Marsh, DJ Weremowicz, S Morton, CC Williams, DM Eng, C
Citation: Sf. Ahmed et al., Balanced translocation of 10q and 13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome, J CLIN END, 84(12), 1999, pp. 4665-4670
Novel isoform of lymphoid adaptor FYN-T-binding protein (FYB-130) interacts with SLP-76 and up-regulates interleukin 2 production
Authors: Veale, M Raab, M Li, ZW da Silva, AJ Kraeft, SK Weremowicz, S Morton, CC Rudd, CE
Citation: M. Veale et al., Novel isoform of lymphoid adaptor FYN-T-binding protein (FYB-130) interacts with SLP-76 and up-regulates interleukin 2 production, J BIOL CHEM, 274(40), 1999, pp. 28427-28435
Risultati: 1-21 |