AAAAAA

   
Results: 1-8 |
Results: 8
SOCS1 deficiency results in accelerated mammary gland development and rescues lactation in prolactin receptor-deficient mice
Authors: Lindeman, GJ Wittlin, S Lada, H Naylor, MJ Santamaria, M Zhang, JG Starr, R Hilton, DJ Alexander, WS Ormandy, CJ Visvader, J
Citation: Gj. Lindeman et al., SOCS1 deficiency results in accelerated mammary gland development and rescues lactation in prolactin receptor-deficient mice, GENE DEV, 15(13), 2001, pp. 1631-1636
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
Authors: Boycott, KM Maybaum, TA Naylor, MJ Weleber, RG Robitaille, J Miyake, Y Bergen, AAB Pierpont, ME Pearce, WG Bech-Hansen, NT
Citation: Km. Boycott et al., A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants, HUM GENET, 108(2), 2001, pp. 91-97
Identification of canine coronavirus strains from feces by S gene nested PCR and molecular characterization of a new Australian isolate
Authors: Naylor, MJ Harrison, GA Monckton, RP McOrist, S Lehrbach, PR Deane, EM
Citation: Mj. Naylor et al., Identification of canine coronavirus strains from feces by S gene nested PCR and molecular characterization of a new Australian isolate, J CLIN MICR, 39(3), 2001, pp. 1036-1041
Canine caronavirus in Australian dogs
Authors: Naylor, MJ Monckton, RP Lehrbach, PR Deane, EM
Citation: Mj. Naylor et al., Canine caronavirus in Australian dogs, AUST VET J, 79(2), 2001, pp. 116-119
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, causeX-linked complete congenital stationary night blindness
Authors: Bech-Hansen, NT Naylor, MJ Maybaum, TA Sparkes, RL Koop, B Birch, DG Bergen, AAB Prinsen, CFM Polomeno, RC Gal, A Drack, AV Musarella, MA Jacobson, SG Young, RSL Weleber, RG
Citation: Nt. Bech-hansen et al., Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, causeX-linked complete congenital stationary night blindness, NAT GENET, 26(3), 2000, pp. 319-323
Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness
Authors: Naylor, MJ Rancourt, DE Bech-Hansen, NT
Citation: Mj. Naylor et al., Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness, GENOMICS, 66(3), 2000, pp. 324-327
Optimization of phase formation and microstructure in Tl-1223 thick films
Authors: Moore, JC Naylor, MJ Grovenor, CRM
Citation: Jc. Moore et al., Optimization of phase formation and microstructure in Tl-1223 thick films, IEEE APPL S, 9(2), 1999, pp. 1787-1790
Melt processing of Bi-2212 on MgO and MgO-buffered substrates
Authors: Naylor, MJ Grovenor, CRM
Citation: Mj. Naylor et Crm. Grovenor, Melt processing of Bi-2212 on MgO and MgO-buffered substrates, IEEE APPL S, 9(2), 1999, pp. 1860-1863
Risultati: 1-8 |