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Results: 1-17 |
Results: 17
Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus (vol 11, pg 208, 2001)
Authors: Edelmann, L Stankiewicz, P Spiteri, E Pandita, RK Shaffer, L Lupski, J Morrow, BE
Citation: L. Edelmann et al., Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus (vol 11, pg 208, 2001), GENOME RES, 11(3), 2001, pp. 503-503
Two function copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus
Authors: Edelmann, L Stankiewicz, P Spiteri, E Pandita, RK Shaffer, L Lupski, J Morrow, BE
Citation: L. Edelmann et al., Two function copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus, GENOME RES, 11(2), 2001, pp. 208-217
Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects
Authors: Funke, B Epstein, JA Kochilas, LK Lu, MM Pandita, RK Liao, J Bauerndistel, R Schuler, T Schorle, H Brown, MC Adams, J Morrow, BE
Citation: B. Funke et al., Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects, HUM MOL GEN, 10(22), 2001, pp. 2549-2556
Characterization of ataxia telangiectasia fibroblasts with extended life-span through telomerase expression
Authors: Wood, LD Halvorsen, TL Dhar, S Baur, JA Pandita, RK Wright, WE Hande, MP Calaf, G Hei, TK Levine, F Shay, JW Wang, JJY Pandita, TK
Citation: Ld. Wood et al., Characterization of ataxia telangiectasia fibroblasts with extended life-span through telomerase expression, ONCOGENE, 20(3), 2001, pp. 278-288
Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11
Authors: Funke, B Pandita, RK Morrow, BE
Citation: B. Funke et al., Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11, GENOMICS, 73(3), 2001, pp. 264-271
TBX1 is responsible for cardiovascular defects in Velo-Cardio-Facial/DiGeorge syndrome
Authors: Merscher, S Funke, B Epstein, JA Heyer, J Puech, A Lu, MM Xavier, RJ Demay, MB Russell, RG Factor, S Tokooya, K Jore, BS Lopez, M Pandita, RK Lia, M Carrion, D Xu, H Schorle, H Kobler, JB Scambler, P Wynshaw-Boris, A Skoultchi, AI Morrow, BE Kucherlapati, R
Citation: S. Merscher et al., TBX1 is responsible for cardiovascular defects in Velo-Cardio-Facial/DiGeorge syndrome, CELL, 104(4), 2001, pp. 619-629
Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome
Authors: Maldonado-Saldivia, J Funke, B Pandita, RK Schuler, T Morrow, BE Schorle, H
Citation: J. Maldonado-saldivia et al., Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome, MECH DEVEL, 96(1), 2000, pp. 121-124
Functional characteristics of urinary tract smooth muscles in mice lackingcGMP protein kinase type I
Authors: Persson, K Pandita, RK Aszodi, A Ahmad, M Pfeifer, A Fassler, R Andersson, KE
Citation: K. Persson et al., Functional characteristics of urinary tract smooth muscles in mice lackingcGMP protein kinase type I, AM J P-REG, 279(3), 2000, pp. R1112-R1120
Cystometric evaluation of bladder function in nonanesthetized mice with and without bladder outlet obstruction
Authors: Pandita, RK Fujiwara, M Alm, P Andersson, KE
Citation: Rk. Pandita et al., Cystometric evaluation of bladder function in nonanesthetized mice with and without bladder outlet obstruction, J UROL, 164(4), 2000, pp. 1385-1389
Intravesical oxyhemoglobin initiates bladder overactivity in conscious, normal rats
Authors: Pandita, RK Mizusawa, H Andersson, KE
Citation: Rk. Pandita et al., Intravesical oxyhemoglobin initiates bladder overactivity in conscious, normal rats, J UROL, 164(2), 2000, pp. 545-550
A common molecular basis for rearrangement disorders on chromosome 22q11
Authors: Edelmann, L Pandita, RK Spiteri, E Funke, B Goldberg, R Palanisamy, N Chaganti, RSK Magenis, E Shprintzen, RJ Morrow, BE
Citation: L. Edelmann et al., A common molecular basis for rearrangement disorders on chromosome 22q11, HUM MOL GEN, 8(7), 1999, pp. 1157-1167
Atm inactivation results in aberrant telomere clustering during meiotic prophase (vol 19, pg 5096, 1999)
Authors: Pandita, TK Westphal, CH Anger, M Sawant, SG Geard, CR Pandita, RK Scherthan, H
Citation: Tk. Pandita et al., Atm inactivation results in aberrant telomere clustering during meiotic prophase (vol 19, pg 5096, 1999), MOL CELL B, 19(9), 1999, pp. 6469-6469
Atm inactivation results in aberrant telomere clustering during meiotic prophase
Authors: Pandita, TK Westphal, CH Anger, M Sawant, SG Geard, CR Pandita, RK Scherthan, H
Citation: Tk. Pandita et al., Atm inactivation results in aberrant telomere clustering during meiotic prophase, MOL CELL B, 19(7), 1999, pp. 5096-5105
Effects of intravesical administration of the K+ channel opener, ZD6169, in conscious rats with and without bladder outflow obstruction
Authors: Pandita, RK Andersson, KE
Citation: Rk. Pandita et Ke. Andersson, Effects of intravesical administration of the K+ channel opener, ZD6169, in conscious rats with and without bladder outflow obstruction, J UROL, 162(3), 1999, pp. 943-948
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation
Authors: Edelmann, L Spiteri, E McCain, N Goldberg, R Pandita, RK Duong, S Fox, J Blumenthal, D Lalani, SR Shaffer, LG Morrow, BE
Citation: L. Edelmann et al., A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation, AM J HU GEN, 65(6), 1999, pp. 1608-1616
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome
Authors: Edelmann, L Pandita, RK Morrow, BE
Citation: L. Edelmann et al., Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome, AM J HU GEN, 64(4), 1999, pp. 1076-1086
Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a1.5-Mb region of overlap on chromosome 22q11
Authors: Funke, B Edelmann, L McCain, N Pandita, RK Ferreira, J Merscher, S Zohouri, M Cannizzaro, L Shanske, A Morrow, BE
Citation: B. Funke et al., Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a1.5-Mb region of overlap on chromosome 22q11, AM J HU GEN, 64(3), 1999, pp. 747-758
Risultati: 1-17 |