Skip Header

 

18 results for author:"Baxter L."Drop in Literature Citations

Customize display Download...

Page 1 of 1

Longitudinal modeling of age-related memory decline and the APOE epsilon4 effect.

Caselli R.J., Dueck A.C., Osborne D., Sabbagh M.N., Connor D.J., Ahern G.L., Baxter L.C., Rapcsak S.Z., Shi J., Woodruff B.K. et al.

N. Engl. J. Med. 361:255-263(2009) · Mapped (6)

Gpnmb is a melanoblast-expressed, MITF-dependent gene.

Loftus S.K., Antonellis A., Matera I., Renaud G., Baxter L.L., Reid D., Wolfsberg T.G., Chen Y., Wang C., Prasad M.K. et al.

Pigment Cell Melanoma Res 22:99-110(2009) · Mapped (21)

A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy.

Matera I., Watkins-Chow D.E., Loftus S.K., Hou L., Incao A., Silver D.L., Rivas C., Elliott E.C., Baxter L.L., Pavan W.J.

Hum. Mol. Genet. 17:2118-2131(2008) · Mapped (19)

IGF binding protein-3 regulates hematopoietic stem cell and endothelial precursor cell function during vascular development.

Chang K.H., Chan-Ling T., McFarland E.L., Afzal A., Pan H., Baxter L.C., Shaw L.C., Caballero S., Sengupta N., Li Calzi S. et al.

Proc. Natl. Acad. Sci. U.S.A. 104:10595-10600(2007) · Mapped (4)

Defective cerebellar response to mitogenic Hedgehog signaling in Down syndrome mice.

Roper R.J., Baxter L.L., Saran N.G., Klinedinst D.K., Beachy P.A., Reeves R.H.

Proc. Natl. Acad. Sci. U.S.A. 103:1452-1456(2006) · Mapped (12)

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage.

Hakami R.M., Hou L., Baxter L.L., Loftus S.K., Southard-Smith E.M., Incao A., Cheng J., Pavan W.J.

Mech. Dev. 123:124-134(2006) · Mapped (20)

Expression of vascular endothelial growth factor and its receptors in the central nervous system in amyotrophic lateral sclerosis.

Brockington A., Wharton S.B., Fernando M., Gelsthorpe C.H., Baxter L., Ince P.G., Lewis C.E., Shaw P.J.

J. Neuropathol. Exp. Neurol. 65:26-36(2006) · Mapped (8)

The transcriptional landscape of the mammalian genome.

Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B., Wells C. et al.

Science 309:1559-1563(2005) · UniProtKB (27,424) · Mapped (12,732)

Longitudinal changes in cognition and behavior in asymptomatic carriers of the APOE e4 allele.

Caselli R.J., Reiman E.M., Osborne D., Hentz J.G., Baxter L.C., Hernandez J.L., Alexander G.G.

Neurology 62:1990-1995(2004) · Mapped (6)

Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development.

Baxter L.L., Pavan W.J.

Gene Expr. Patterns 3:703-707(2003) · Mapped (14)

Expression of interleukin-6 and its effects on growth of HP75 human pituitary tumor cells.

Borg S.A., Kerry K.E., Baxter L., Royds J.A., Jones T.H.

J. Clin. Endocrinol. Metab. 88:4938-4944(2003) · Mapped (6)

Apolipoprotein E epsilon 4 affects new learning in cognitively normal individuals at risk for Alzheimer's disease.

Baxter L.C., Caselli R.J., Johnson S.C., Reiman E., Osborne D.

Neurobiol. Aging 24:947-952(2003) · Mapped (6)

Depletion of Langerhans cells in human papillomavirus type 16-infected skin is associated with E6-mediated down regulation of E-cadherin.

Matthews K., Leong C.M., Baxter L., Inglis E., Yun K., Backstrom B.T., Doorbar J., Hibma M.

J. Virol. 77:8378-8385(2003) · Mapped (7)

The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development.

Baxter L.L., Pavan W.J.

Mech. Dev. 116:209-212(2002) · Mapped (7)

Mutation of melanosome protein RAB38 in chocolate mice.

Loftus S.K., Larson D.M., Baxter L.L., Antonellis A., Chen Y., Wu X., Jiang Y., Bittner M., Hammer J.A. III, Pavan W.J.

Proc. Natl. Acad. Sci. U.S.A. 99:4471-4476(2002) · UniProtKB (1) · Mapped (18)

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.

Applebury M.L., Antoch M.P., Baxter L.C., Chun L.Y., Falk J.D., Farhangfar F., Kage K., Krzystolik M.G., Lyass L.A., Robbins J.T.

Neuron 27:513-523(2000) · UniProtKB (2) · Mapped (4)

Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16.

Moore C.S., Lee J.S., Birren B., Stetten G., Baxter L.L., Reeves R.H.

Genomics 59:1-5(1999) · Mapped (12)

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.

Bowes C., Li T., Danciger M., Baxter L.C., Applebury M.L., Farber D.B.

Nature 347:677-680(1990) · UniProtKB (1) · Mapped (6)

Page 1 of 1