Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics

Por Karp, Natasha A., Heller, Ruth, Yaacoby, Shay, White, Jacqueline K., Benjamini, Yoav
Publicado no Genetics (2017)

Incomplete glycosylation and defective intracellular targeting of mutant solute carrier family 11 member 1 (Slc11a1)

Por White, Jacqueline K., Stewart, Abigail, Popoff, Jean-Francois, Wilson, Shona, Blackwell, Jenefer M.
Publicado em 2004

The mouse genetics toolkit: revealing function and mechanism

Por van der Weyden, Louise, White, Jacqueline K, Adams, David J, Logan, Darren W
Publicado em 2011

Slc11a1, Formerly Nramp1, Is Expressed in Dendritic Cells and Influences Major Histocompatibility Complex Class II Expression and Antigen-Presenting Cell Function

Por Stober, Carmel B., Brode, Sven, White , Jacqueline K., Popoff, Jean-François, Blackwell, Jenefer M.
Publicado em 2007

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1

Por Bosman, Erika A., Estabel, Jeanne, Ismail, Ozama, Podrini, Christine, White, Jacqueline K., Steel, Karen P.
Publicado em 2012

Reporting phenotypes in mouse models when considering body size as a potential confounder

Por Oellrich, Anika, Meehan, Terrence F., Parkinson, Helen, Sarntivijai, Sirarat, White, Jacqueline K., Karp, Natasha A.
Publicado no J Biomed Semantics (2016)

The fallacy of Ratio Correction to address confounding factors

Por Karp, Natasha A, Segonds-Pichon, Anne, Gerdin, Anna-Karin B, Ramírez-Solis, Ramiro, White, Jacqueline K
Publicado em 2012

Optimising experimental design for high-throughput phenotyping in mice: a case study

Por Karp, Natasha A., Baker, Lauren A., Gerdin, Anna-Karin B., Adams, Niels C., Ramírez-Solis, Ramiro, White, Jacqueline K.
Publicado em 2010

Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies

Por Karp, Natasha A., Speak, Anneliese O., White, Jacqueline K., Adams, David J., Hrabé de Angelis, Martin, Hérault, Yann, Mott, Richard F.
Publicado em 2014

Mouse Slc9a8 Mutants Exhibit Retinal Defects Due to Retinal Pigmented Epithelium Dysfunction

Por Jadeja, Shalini, Barnard, Alun R., McKie, Lisa, Cross, Sally H., White, Jacqueline K., Robertson, Morag, Budd, Peter S., MacLaren, Robert E., Jackson, Ian J.
Publicado no Invest Ophthalmol Vis Sci (2015)

SLC11A1 (formerly NRAMP1) and disease resistance

Por Blackwell, Jenefer M., Goswami, Tapasree, Evans, Carlton A. W., Sibthorpe, Dean, Papo, Natalie, White, Jacqueline K., Searle, Susan, Miller, E. Nancy, Peacock, Christopher S., Mohammed, Hiba, Ibrahim, Muntaser
Publicado em 2001

Modeling Partial Monosomy for Human Chromosome 21q11.2-q21.1 Reveals Haploinsufficient Genes Influencing Behavior and Fat Deposition

Por Migdalska, Anna M., van der Weyden, Louise, Ismail, Ozama, White, Jacqueline K., Project, Sanger Mouse Genetics, Sánchez-Andrade, Gabriela, Logan, Darren W., Arends, Mark J., Adams, David J.
Publicado em 2012

Correction: Modeling Partial Monosomy for Human Chromosome 21q11.2-q21.1 Reveals Haploinsufficient Genes Influencing Behavior and Fat Deposition

Por Migdalska, Anna M., van der Weyden, Louise, Ismail, Ozama, White, Jacqueline K., Sanger Mouse Genetics Project, Sánchez-Andrade, Gabriela, Logan, Darren W., Arends, Mark J., Adams, David J.
Publicado em 2012

Experimental and husbandry procedures as potential modifiers of the results of phenotyping tests

Por Gerdin, Anna-Karin, Igosheva, Natalia, Roberson, Laura-Anne, Ismail, Ozama, Karp, Natasha, Sanderson, Mark, Cambridge, Emma, Shannon, Carl, Sunter, David, Ramirez-Solis, Ramiro, Bussell, James, White, Jacqueline K.
Publicado em 2012

High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice

Por Podrini, Christine, Cambridge, Emma L., Lelliott, Christopher J., Carragher, Damian M., Estabel, Jeanne, Gerdin, Anna-Karin, Karp, Natasha A., Scudamore, Cheryl L., Ramirez-Solis, Ramiro, White, Jacqueline K.
Publicado em 2013

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

Por Ingham, Neil J., Carlisle, Francesca, Pearson, Selina, Lewis, Morag A., Buniello, Annalisa, Chen, Jing, Isaacson, Rivka L., Pass, Johanna, White, Jacqueline K., Dawson, Sally J., Steel, Karen P.
Publicado no Sci Rep (2016)

Generation of the Sotos syndrome deletion in mice

Por Migdalska, Anna M., van der Weyden, Louise, Ismail, Ozama, Rust, Alistair G., Rashid, Mamunur, White, Jacqueline K., Sánchez-Andrade, Gabriela, Lupski, James R., Logan, Darren W., Arends, Mark J., Adams, David J.
Publicado em 2012

Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen

Por Liakath-Ali, Kifayathullah, Vancollie, Valerie E., Heath, Emma, Smedley, Damian P., Estabel, Jeanne, Sunter, David, DiTommaso, Tia, White, Jacqueline K., Ramirez-Solis, Ramiro, Smyth, Ian, Steel, Karen P., Watt, Fiona M.
Publicado em 2014

Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia

Por Salsbury, Grace, Cambridge, Emma L., McIntyre, Zoe, Arends, Mark J., Karp, Natasha A., Isherwood, Christopher, Shannon, Carl, Hooks, Yvette, Ramirez-Solis, Ramiro, Adams, David J., White, Jacqueline K., Speak, Anneliese O.
Publicado no Exp Hematol (2014)

Corrigendum to “Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia” [Experimental Hematology, Vol. 42, Issue 12, p1053–1058.e1]

Por Salsbury, Grace, Cambridge, Emma L., McIntyre, Zoe, Arends, Mark J., Karp, Natasha A., Isherwood, Christopher, Shannon, Carl, Hooks, Yvette, Ramirez-Solis, Ramiro, Adams, David J., White, Jacqueline K., Speak, Anneliese O.
Publicado no Exp Hematol (2015)