B-Cells and Antibodies in Old Humans

door Gibson, Kate L., Dunn-Walters, Deborah K.
Gepubliceerd in Handbook on Immunosenescence (2008)

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

door Shannon, Kate, Bright, Vicki, Gibson, Kate, Tyndall, Mark W.
Gepubliceerd in Can J Public Health (2007)

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

door Gibson Kate, Deering Kathleen, Duff Putu, Tyndall Mark, Shannon Kate
Gepubliceerd in 2011-08-01

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

door Duff, Putu, Deering, Kathleen, Gibson, Kate, Tyndall, Mark, Shannon, Kate
Gepubliceerd in 2011

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

door Kim, Rachel, Goldenberg, Shira, Duff, Putu, Nguyen, Paul, Gibson, Kate, Shannon, Kate
Gepubliceerd in Int J Gynaecol Obstet (2014)

Molecular chaperone Hsp27 regulates the Hippo tumor suppressor pathway in cancer

door Vahid, Sepideh, Thaper, Daksh, Gibson, Kate F., Bishop, Jennifer L., Zoubeidi, Amina
Gepubliceerd in Sci Rep (2016)

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

door Shannon, Kate, Bright, Vicki, Allinott, Shari, Alexson, Debbie, Gibson, Kate, Tyndall, Mark W
Gepubliceerd in 2007

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

door Janssen, Patricia A., Gibson, Kate, Bowen, Raven, Spittal, Patricia M., Petersen, Karen L.
Gepubliceerd in 2009

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

door Lazarus, Lisa, Deering, Kathleen N, Nabess, Rose, Gibson, Kate, Tyndall, Mark W, Shannon, Kate
Gepubliceerd in 2011

Screening for pre-clinical disability in different residential settings

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

Screening for pre-clinical disability in different residential settings

door Gibson, Kate, Day, Lesley, Hill, Keith D, Jolley, Damien, Newstead, Stuart, Cicuttini, Flavia, Segal, Leonie, Flicker, Leon
Gepubliceerd in 2010

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

door 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
Gepubliceerd in 2009

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

door 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
Gepubliceerd in 2009

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

door 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.
Gepubliceerd in Mol Genet Genomic Med (2018)

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

door 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
Gepubliceerd in 2009

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

door 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.
Gepubliceerd in Nat Genet (2018)

Clinical and genetic aspects of KBG syndrome

door 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
Gepubliceerd in Am J Med Genet A (2016)

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

door 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
Gepubliceerd in 2010

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

door 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
Gepubliceerd in 2010

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

door 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
Gepubliceerd in 2010