Genetic predisposition to peripheral nerve neoplasia: Diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes

Por Rodriguez, Fausto J., Stratakis, Constantine A., Evans, D Gareth
Publicado em 2011

Identification of a gene set to evaluate the potential effects of loud sounds from seismic surveys on the ears of fishes: a study with Salmo salar

Por Andrews, C D, Payne, J F, Rise, M L
Publicado no J Fish Biol (2014)

A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?

Por Murray, A J, Hughes, T A T, Neal, J W, Howard, E, Evans, D G R, Harper, P S
Publicado em 2006

BTG1, a member of a new family of antiproliferative genes.

Por Rouault, J P, Rimokh, R, Tessa, C, Paranhos, G, Ffrench, M, Duret, L, Garoccio, M, Germain, D, Samarut, J, Magaud, J P
Publicado em 1992

Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient

Por McColgan, P., Viegas, S., Gandhi, S., Bull, K., Tudor, R., Sheikh, F., Pinney, J., Fontana, M., Rowczenio, D., Gillmore, J. D., Gilbertson, J. A., Whelan, C. J., Shah, S., Jaunmuktane, Z., Holton, J. L., Schott, J. M., Werring, D. J., Hawkins, P. N., Reilly, M. M.
Publicado no J Neurol (2014)

Atrial myxoma: a tumour in search of its origins.

Por Krikler, D M, Rode, J, Davies, M J, Woolf, N, Moss, E
Publicado em 1992

Mass spectrometry analysis reveals non-mutated ApoA1 lumbosacral radiculoplexus amyloidoma

Por Loavenbruck, Adam J., Chaudhry, Vinay, Zeldenrust, Steven R., Spinner, Robert J., Theis, Jason D., Klein, Christopher J.
Publicado em 2012

A Novel Missense Mutation in ADAMTS10 in Norwegian Elkhound Primary Glaucoma

Por Ahonen, Saija J., Kaukonen, Maria, Nussdorfer, Forrest D., Harman, Christine D., Komáromy, András M., Lohi, Hannes
Publicado no PLoS One (2014)

Genetic variation in the HLA region is associated with susceptibility to herpes zoster

Por Crosslin, D R, Carrell, D S, Burt, A, Kim, D S, Underwood, J G, Hanna, D S, Comstock, B A, Baldwin, E, de Andrade, M, Kullo, I J, Tromp, G, Kuivaniemi, H, Borthwick, K M, McCarty, C A, Peissig, P L, Doheny, K F, Pugh, E, Kho, A, Pacheco, J, Hayes, M G, Ritchie, M D, Verma, S S, Armstrong, G, Stallings, S, Denny, J C, Carroll, R J, Crawford, D C, Crane, P K, Mukherjee, S, Bottinger, E, Li, R, Keating, B, Mirel, D B, Carlson, C S, Harley, J B, Larson, E B, Jarvik, G P
Publicado no Genes Immun (2015)

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Por Pham-Dinh, D, Popot, J L, Boespflug-Tanguy, O, Landrieu, P, Deleuze, J F, Boué, J, Jollès, P, Dautigny, A
Publicado em 1991

Expression of FGFR-2 and FGFR-3 in the normal human fetal orbit

Por Khan, S H, Britto, J A, Evans, R D, Nischal, K K
Publicado em 2005

Computational Simulation Expands Understanding of Electrotransfer-Based Gene Augmentation for Enhancement of Neural Interfaces

Por Amr Al Abed, Jeremy L. Pinyon, Evelyn Foster, Frederik Crous, Gary J. Cowin, Gary D. Housley, Nigel H. Lovell
Publicado em 2019-08-01

NTRK-1 fusion in endocervical fibroblastic malignant peripheral nerve sheath tumor marking eligibility for larotrectinib therapy: A case report

Por Wells, A.E., Mallen, A.M., Bui, M.M., Reed, D.R., Apte, S.M.
Publicado no Gynecol Oncol Rep (2019)

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

Por Jongmans, M C J, Admiraal, R J, van der Donk, K P, Vissers, L E L M, Baas, A F, Kapusta, L, van Hagen, J M, Donnai, D, de Ravel, T J, Veltman, J A, van Kessel, A Geurts, De Vries, B B A, Brunner, H G, Hoefsloot, L H, van Ravenswaaij, C M A
Publicado em 2006

Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside

Por Koilkonda, Rajeshwari D., Guy, John
Publicado em 2011

Nerve growth factor regulates gene expression by several distinct mechanisms.

Por Cho, K O, Skarnes, W C, Minsk, B, Palmieri, S, Jackson-Grusby, L, Wagner, J A
Publicado em 1989

Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns.

Por Sekido, Y, Bader, S, Latif, F, Chen, J Y, Duh, F M, Wei, M H, Albanesi, J P, Lee, C C, Lerman, M I, Minna, J D
Publicado em 1996

Regulatory peptides in the respiratory tract of Macaca fascicularis.

Por Ghatei, M A, Springall, D R, Richards, I M, Oostveen, J A, Griffin, R L, Cadieux, A, Polak, J M, Bloom, S R
Publicado em 1987

p53 Protein overexpression in cholangiocarcinoma arising in primary sclerosing cholangitis.

Por Rizzi, P M, Ryder, S D, Portmann, B, Ramage, J K, Naoumov, N V, Williams, R
Publicado em 1996

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy

Por Hall, Thomas E., Bryson-Richardson, Robert J., Berger, Silke, Jacoby, Arie S., Cole, Nicholas J., Hollway, Georgina E., Berger, Joachim, Currie, Peter D.
Publicado em 2007