H
Helen J. Eyre
Researcher at Boston Children's Hospital
Publications - 78
Citations - 5308
Helen J. Eyre is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Gene & Gene mapping. The author has an hindex of 36, co-authored 78 publications receiving 5121 citations. Previous affiliations of Helen J. Eyre include University of Adelaide & Women's and Children's Hospital.
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Journal ArticleDOI
Fc alpha/mu receptor mediates endocytosis of IgM-coated microbes.
Akira Shibuya,Norihisa Sakamoto,Norihisa Sakamoto,Yoshio Shimizu,Kazuko Shibuya,Kazuko Shibuya,Mitsujiro Osawa,Takashi Hiroyama,Helen J. Eyre,Grant R. Sutherland,Yuichi Endo,Teizo Fujita,Tomoyuki Miyabayashi,Seiji Sakano,Takao Tsuji,Eiichi Nakayama,Joseph H. Phillips,Lewis L. Lanier,Hiromitsu Nakauchi +18 more
TL;DR: A mouse Fc receptor, designated Fcα/μR, and its human homolog, that bind both IgM and IgA with intermediate or high affinity are described that are involved in the primary stages of the immune response to microbes.
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MUC13, a Novel Human Cell Surface Mucin Expressed by Epithelial and Hemopoietic Cells
Stephanie J. Williams,Daniel H. Wreschner,Mai Tran,Helen J. Eyre,Grant R. Sutherland,Michael A. McGuckin +5 more
TL;DR: In situ hybridization in murine tissues revealed expression in intestinal epithelial and lymphoid cells, and Immunohistochemistry demonstrated the human MUC13 protein on the apical membrane of both columnar and goblet cells in the gastrointestinal tract, indicative of secretion in addition to presence on the cell surface.
Journal Article
Two novel mucin genes down-regulated in colorectal cancer identified by differential display.
Stephanie J. Williams,Michael A. McGuckin,David C. Gotley,Helen J. Eyre,Grant R. Sutherland,Toni M. Antalis +5 more
TL;DR: Structural homology of MUC11 with rat, mouse, and human MUC3 and human and rat MUC4/ASGP2 indicate that there is a distinct subfamily of transmembrane mucins with conserved epidermal growth factor domains, and suggests that MUC12 may be involved in epithelial cell growth regulation.
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Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation
Vera M. Kalscheuer,Jiong Tao,A. Donnelly,Georgina Hollway,Eberhard Schwinger,S. Kübart,Corinna Menzel,Maria Hoeltzenbein,Niels Tommerup,Helen J. Eyre,Michael G. Harbord,Eric Haan,Grant R. Sutherland,Hans-Hilger Ropers,Jozef Gecz +14 more
TL;DR: A study of two severely affected female patients with apparently de novo balanced X;autosome translocations, both disrupting the serine-threonine kinase 9 (STK9) gene, shows that STK9 is subject to X-inactivation in normal female somatic cells and is functionally absent in the two patients, because of preferential inactivation of the normal X.
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Identification of SOX3 as an XX male sex reversal gene in mice and humans
Edwina Sutton,James N. Hughes,Stefan J. White,Ryohei Sekido,Jacqueline Tan,Valerie A. Arboleda,Nicholas Rogers,Kevin Christopher Knower,L. Rowley,Helen J. Eyre,Karine Rizzoti,Dale McAninch,João Gonçalves,Jennie Slee,Erin Turbitt,D L Bruno,Henrik Bengtsson,Vincent R. Harley,Eric Vilain,Andrew H. Sinclair,Robin Lovell-Badge,Paul Q. Thomas +21 more
TL;DR: SOX3 and SRY are functionally interchangeable in sex determination and support the notion that SRY evolved from SOX3 via a regulatory mutation that led to its de novo expression in the early gonad.