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 2010

Genome editing: A perspective on the application of CRISPR/Cas9 to study human diseases (Review)

por Rodríguez-Rodríguez, Diana Raquel, Ramírez-Solís, Ramiro, Garza-Elizondo, Mario Alberto, De Lourdes Garza-Rodríguez, María, Barrera-Saldaña, Hugo Alberto
Publicado 2019

A staging system for correct phenotype interpretation of mouse embryos harvested on embryonic day 14 (E14.5)

por Geyer, Stefan H., Reissig, Lukas, Rose, Julia, Wilson, Robert, Prin, Fabrice, Szumska, Dorota, Ramirez‐Solis, Ramiro, Tudor, Catherine, White, Jacqui, Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2017

MRNIP interacts with sex body chromatin to support meiotic progression, spermatogenesis, and male fertility in mice

por Kazi, Samina, Castañeda, Julio M., Savolainen, Audrey, Xu, Yiding, Liu, Ning, Qiao, Huanyu, Ramirez‐Solis, Ramiro, Nozawa, Kaori, Yu, Zhifeng, Matzuk, Martin M., Prunskaite‐Hyyryläinen, Renata
Publicado 2022

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 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 2013

Genomic Analysis of a Novel Spontaneous Albino C57BL/6N Mouse Strain

por Ryder, Edward, Wong, Kim, Gleeson, Diane, Keane, Thomas M, Sethi, Debarati, Vyas, Sapna, Wardle-Jones, Hannah, Bussell, James N, Houghton, Richard, Salisbury, Jennifer, Harvey, Nina, Adams, David J, Ramirez-Solis, Ramiro
Publicado 2013

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 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 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 2015

An Orphan CpG Island Drives Expression of a let-7 miRNA Precursor with an Important Role in Mouse Development

por Koerner, Martha V., Chhatbar, Kashyap, Webb, Shaun, Cholewa-Waclaw, Justyna, Selfridge, Jim, De Sousa, Dina, Skarnes, Bill, Rosen, Barry, Thomas, Mark, Bottomley, Joanna, Ramirez-Solis, Ramiro, Lelliott, Christopher, Adams, David J., Bird, Adrian
Publicado 2019

Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse

por DiTommaso, Tia, Jones, Lynelle K., Cottle, Denny L., Gerdin, Anna-Karin, Vancollie, Valerie E., Watt, Fiona M., Ramirez-Solis, Ramiro, Bradley, Allan, Steel, Karen P., Sundberg, John P., White, Jacqueline K., Smyth, Ian M.
Publicado 2014

Rapid-Throughput Skeletal Phenotyping of 100 Knockout Mice Identifies 9 New Genes That Determine Bone Strength

por Bassett, J. H. Duncan, Gogakos, Apostolos, White, Jacqueline K., Evans, Holly, Jacques, Richard M., van der Spek, Anne H., Ramirez-Solis, Ramiro, Ryder, Edward, Sunter, David, Boyde, Alan, Campbell, Michael J., Croucher, Peter I., Williams, Graham R.
Publicado 2012

Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource

por Ryder, Edward, Gleeson, Diane, Sethi, Debarati, Vyas, Sapna, Miklejewska, Evelina, Dalvi, Priya, Habib, Bishoy, Cook, Ross, Hardy, Matthew, Jhaveri, Kalpesh, Bottomley, Joanna, Wardle-Jones, Hannah, Bussell, James N., Houghton, Richard, Salisbury, Jennifer, Skarnes, William C., Ramirez-Solis, Ramiro
Publicado 2013

Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase

por Ryder, Edward, Doe, Brendan, Gleeson, Diane, Houghton, Richard, Dalvi, Priya, Grau, Evelyn, Habib, Bishoy, Miklejewska, Evelina, Newman, Stuart, Sethi, Debarati, Sinclair, Caroline, Vyas, Sapna, Wardle-Jones, Hannah, Bottomley, Joanna, Bussell, James, Galli, Antonella, Salisbury, Jennifer, Ramirez-Solis, Ramiro
Publicado 2013

Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach

por Scavizzi, Ferdinando, Ryder, Edward, Newman, Stuart, Raspa, Marcello, Gleeson, Diane, Wardle-Jones, Hannah, Montoliu, Lluis, Fernandez, Almudena, Dessain, Marie-Laure, Larrigaldie, Vanessa, Khorshidi, Zuzana, Vuolteenaho, Reetta, Soininen, Raija, André, Philippe, Jacquot, Sylvie, Hong, Yi, de Angelis, Martin Hrabe, Ramirez-Solis, Ramiro, Doe, Brendan
Publicado 2015

Highly variable penetrance of abnormal phenotypes in embryonic lethal knockout mice

por Wilson, Robert, Geyer, Stefan H., Reissig, Lukas, Rose, Julia, Szumska, Dorota, Hardman, Emily, Prin, Fabrice, McGuire, Christina, Ramirez-Solis, Ramiro, White, Jacqui, Galli, Antonella, Tudor, Catherine, Tuck, Elizabeth, Mazzeo, Cecilia Icoresi, Smith, James C., Robertson, Elizabeth, Adams, David J., Mohun, Timothy, Weninger, Wolfgang J.
Publicado 2017

Targeting of Slc25a21 Is Associated with Orofacial Defects and Otitis Media Due to Disrupted Expression of a Neighbouring Gene

por Maguire, Simon, Estabel, Jeanne, Ingham, Neil, Pearson, Selina, Ryder, Edward, Carragher, Damian M., Walker, Nicolas, Bussell, James, Chan, Wai-In, Keane, Thomas M., Adams, David J., Scudamore, Cheryl L., Lelliott, Christopher J., Ramírez-Solis, Ramiro, Karp, Natasha A., Steel, Karen P., White, Jacqueline K., Gerdin, Anna-Karin
Publicado 2014

A gene expression resource generated by genome-wide lacZ profiling in the mouse

por Tuck, Elizabeth, Estabel, Jeanne, Oellrich, Anika, Maguire, Anna Karin, Adissu, Hibret A., Souter, Luke, Siragher, Emma, Lillistone, Charlotte, Green, Angela L., Wardle-Jones, Hannah, Carragher, Damian M., Karp, Natasha A., Smedley, Damian, Adams, Niels C., Bussell, James N., Adams, David J., Ramírez-Solis, Ramiro, Steel, Karen P., Galli, Antonella, White, Jacqueline K.
Publicado 2015

Disruption of Mouse Cenpj, a Regulator of Centriole Biogenesis, Phenocopies Seckel Syndrome

por McIntyre, Rebecca E., Lakshminarasimhan Chavali, Pavithra, Ismail, Ozama, Carragher, Damian M., Sanchez-Andrade, Gabriela, Forment, Josep V., Fu, Beiyuan, Del Castillo Velasco-Herrera, Martin, Edwards, Andrew, van der Weyden, Louise, Yang, Fengtang, Ramirez-Solis, Ramiro, Estabel, Jeanne, Gallagher, Ferdia A., Logan, Darren W., Arends, Mark J., Tsang, Stephen H., Mahajan, Vinit B., Scudamore, Cheryl L., White, Jacqueline K., Jackson, Stephen P., Gergely, Fanni, Adams, David J.
Publicado 2012