Analyses of multiple single-nucleotide polymorphisms in the SUMO4/IDDM5 region in affected sib-pair families with type I diabetes

Por Podolsky, R, Linga-Reddy, MV Prasad, She, J-X
Publicado em 2009

Association of LMP2 and LMP7 genes within the major histocompatibility complex with insulin-dependent diabetes mellitus: population and family studies.

Por Deng, G Y, Muir, A, Maclaren, N K, She, J X
Publicado em 1995

Amplification of major histocompatibility complex class II gene diversity by intraexonic recombination.

Por She, J X, Boehme, S A, Wang, T W, Bonhomme, F, Wakeland, E K
Publicado em 1991

Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24.

Por Wang, C Y, Hawkins-Lee, B, Ochoa, B, Walker, R D, She, J X
Publicado em 1997

Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27.

Por Luo, D F, Bui, M M, Muir, A, Maclaren, N K, Thomson, G, She, J X
Publicado em 1995

Independent variation and positive selection in env V1 and V2 domains within maternal-infant strains of human immunodeficiency virus type 1 in vivo.

Por Lamers, S L, Sleasman, J W, She, J X, Barrie, K A, Pomeroy, S M, Barrett, D J, Goodenow, M M
Publicado em 1993

Persistence of multiple maternal genotypes of human immunodeficiency virus type I in infants infected by vertical transmission.

Por Lamers, S L, Sleasman, J W, She, J X, Barrie, K A, Pomeroy, S M, Barrett, D J, Goodenow, M M
Publicado em 1994

Family cell lines available for research--an endangered resource?

Por Lernmark, A, Eisenbarth, G, Ducat, L, Erlich, H A, Faustman, D, Maclaren, N K, Ott, J, Permutt, M A, She, J X, Todd, J
Publicado em 1997

Next-generation sequencing for viruses in children with rapid-onset type 1 diabetes

Por Lee, H-S., Briese, T., Winkler, C., Rewers, M., Bonifacio, E., Hyoty, H., Pflueger, M., Simell, O., She, J. X., Hagopian, W., Lernmark, Å., Akolkar, B., Krischer, J., Ziegler, A. G.
Publicado em 2013

Aberrant prostaglandin synthase 2 expression defines an antigen-presenting cell defect for insulin-dependent diabetes mellitus

Por Litherland, S.A., Xie, X.T., Hutson, A.D., Wasserfall, C., Whittaker, D.S., She, J.-X., Hofig, A., Dennis, M.A., Fuller, K., Cook, R., Schatz, D., Moldawer, L.L., Clare-Salzler, M.J.
Publicado em 1999

Country-specific birth weight and length in type 1 diabetes high-risk HLA genotypes in combination with prenatal characteristics

Por Sterner, Y, Törn, C, Lee, H-S, Larsson, H, Winkler, C, McLeod, W, Lynch, K, Simell, O, Ziegler, A, Schatz, D, Hagopian, W, Rewers, M, She, J-X, Krischer, J P, Akolkar, B, Lernmark, Å
Publicado em 2011

RhoA S-nitrosylation as a regulatory mechanism influencing endothelial barrier function in response to G(+)-bacterial toxins

Por Chen, F., Wang, Y., Rafikov, R., Haigh, S., Zhi, W.B., Kumar, S., Doulias, P.T., Rafikova, O., Pillich, H., Chakraborty, T., Lucas, R., Verin, A.D., Catravas, J.D., She, J.X., Black, S.M., Fulton, D.J.R.
Publicado no Biochem Pharmacol (2016)

Confirmation of novel type 1 diabetes risk loci in families

Por Cooper, J. D., Howson, J. M. M., Smyth, D., Walker, N. M., Stevens, H., Yang, J. H. M., She, J.-X., Eisenbarth, G. S., Rewers, M., Todd, J. A., Akolkar, B., Concannon, P., Erlich, H. A., Julier, C., Morahan, G., Nerup, J., Nierras, C., Pociot, F., Rich, S. S.
Publicado em 2012