B-Cells and Antibodies in Old Humans

por Gibson, Kate L., Dunn-Walters, Deborah K.
Publicado en Handbook on Immunosenescence (2008)

Sexual and Drug-related Vulnerabilities for HIV Infection Among Women Engaged in Survival Sex Work in Vancouver, Canada

por Shannon, Kate, Bright, Vicki, Gibson, Kate, Tyndall, Mark W.
Publicado en Can J Public Health (2007)

Homelessness among a cohort of women in street-based sex work: the need for safer environment interventions

por Gibson Kate, Deering Kathleen, Duff Putu, Tyndall Mark, Shannon Kate
Publicado 2011-08-01

Homelessness among a cohort of women in street-based sex work: the need for safer environment interventions

por Duff, Putu, Deering, Kathleen, Gibson, Kate, Tyndall, Mark, Shannon, Kate
Publicado 2011

Uptake of a women-only, sex-work-specific drop-in center and links with sexual and reproductive health care for sex workers

por Kim, Rachel, Goldenberg, Shira, Duff, Putu, Nguyen, Paul, Gibson, Kate, Shannon, Kate
Publicado en Int J Gynaecol Obstet (2014)

Molecular chaperone Hsp27 regulates the Hippo tumor suppressor pathway in cancer

por Vahid, Sepideh, Thaper, Daksh, Gibson, Kate F., Bishop, Jennifer L., Zoubeidi, Amina
Publicado en Sci Rep (2016)

Community-based HIV prevention research among substance-using women in survival sex work: The Maka Project Partnership

por Shannon, Kate, Bright, Vicki, Allinott, Shari, Alexson, Debbie, Gibson, Kate, Tyndall, Mark W
Publicado 2007

Peer Support using a Mobile Access Van Promotes Safety and Harm Reduction Strategies among Sex Trade Workers in Vancouver’s Downtown Eastside

por Janssen, Patricia A., Gibson, Kate, Bowen, Raven, Spittal, Patricia M., Petersen, Karen L.
Publicado 2009

Occupational Stigma as a Primary Barrier To Health Care For Street-Based Sex Workers in Canada

por Lazarus, Lisa, Deering, Kathleen N, Nabess, Rose, Gibson, Kate, Tyndall, Mark W, Shannon, Kate
Publicado 2011

Screening for pre-clinical disability in different residential settings

por Newstead Stuart, Jolley Damien, Hill Keith D, Day Lesley, Gibson Kate, Cicuttini Flavia, Segal Leonie, Flicker Leon
Publicado 2010-08-01

Screening for pre-clinical disability in different residential settings

por Gibson, Kate, Day, Lesley, Hill, Keith D, Jolley, Damien, Newstead, Stuart, Cicuttini, Flavia, Segal, Leonie, Flicker, Leon
Publicado 2010

B-cell diversity decreases in old age and is correlated with poor health status

por Gibson, Kate L, Wu, Yu-Chang, Barnett, Yvonne, Duggan, Orla, Vaughan, Robert, Kondeatis, Elli, Nilsson, Bengt-Olof, Wikby, Anders, Kipling, David, Dunn-Walters, Deborah K
Publicado 2009

Novel SOX2 partner-factor domain mutation in a four-generation family

por Mihelec, Marija, Abraham, Peter, Gibson, Kate, Krowka, Renata, Susman, Rachel, Storen, Rebecca, Chen, Yongjuan, Donald, Jenny, Tam, Patrick PL, Grigg, John R, Flaherty, Maree, Gole, Glen A, Jamieson, Robyn V
Publicado 2009

Penetrance and expressivity of the R858H CACNA1C variant in a five‐generation pedigree segregating an arrhythmogenic channelopathy

por Gardner, R. J. McKinlay, Crozier, Ian G., Binfield, Alex L., Love, Donald R., Lehnert, Klaus, Gibson, Kate, Lintott, Caroline J., Snell, Russell G., Jacobsen, Jessie C., Jones, Peter P., Waddell‐Smith, Kathryn E., Kennedy, Martin A., Skinner, Jonathan R.
Publicado en Mol Genet Genomic Med (2018)

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

por Neumann, Thomas E, Allanson, Judith, Kavamura, Ines, Kerr, Bronwyn, Neri, Giovanni, Noonan, Jacqueline, Cordeddu, Viviana, Gibson, Kate, Tzschach, Andreas, Krüger, Gabriele, Hoeltzenbein, Maria, Goecke, Timm O, Kehl, Hans Gerd, Albrecht, Beate, Luczak, Klaudiusz, Sasiadek, Maria M, Musante, Luciana, Laurie, Rohan, Peters, Hartmut, Tartaglia, Marco, Zenker, Martin, Kalscheuer, Vera
Publicado 2009

Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions

por Heyn, Patricia, Logan, Clare V., Fluteau, Adeline, Challis, Rachel C., Auchynnikava, Tatsiana, Martin, Carol-Anne, Marsh, Joseph A., Taglini, Francesca, Kilanowski, Fiona, Parry, David A., Cormier-Daire, Valerie, Fong, Chin-To, Gibson, Kate, Hwa, Vivian, Ibáñez, Lourdes, Robertson, Stephen P., Sebastiani, Giorgia, Rappsilber, Juri, Allshire, Robin C., Reijns, Martin A.M., Dauber, Andrew, Sproul, Duncan, Jackson, Andrew P.
Publicado en Nat Genet (2018)

Clinical and genetic aspects of KBG syndrome

por Low, Karen, Ashraf, Tazeen, Canham, Natalie, Clayton‐Smith, Jill, Deshpande, Charu, Donaldson, Alan, Fisher, Richard, Flinter, Frances, Foulds, Nicola, Fryer, Alan, Gibson, Kate, Hayes, Ian, Hills, Alison, Holder, Susan, Irving, Melita, Joss, Shelagh, Kivuva, Emma, Lachlan, Kathryn, Magee, Alex, McConnell, Vivienne, McEntagart, Meriel, Metcalfe, Kay, Montgomery, Tara, Newbury‐Ecob, Ruth, Stewart, Fiona, Turnpenny, Peter, Vogt, Julie, Fitzpatrick, David, Williams, Maggie, Smithson, Sarah
Publicado en Am J Med Genet A (2016)

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

por van Bon, Bregje W M, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Moloney, Susan, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado 2010

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

por van Bon, Bregje WM, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado 2010

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

por van Bon, Bregje WM, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado 2010