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1. Epigenetic activation of SOX11 is associated with recurrence and progression of ductal carcinoma in situ to invasive breast cancer

Author

Treekitkarnmongkol, Warapen, Shah, Vandna, Kai, Kazuharu, Katayama, Hiroshi, Wong, Justin, Ladha, Farah A., Nguyen, Tristian, Menegaz, Brian, Lu, Wei, Yang, Fei, Mino, Barbara, Tang, Ximing, Gagea, Mihai, Batra, Harsh, Raso, Maria Gabriela, Wistuba, Ignacio I., Krishnamurthy, Savitri, Pinder, Sarah E., Sawyer, Elinor J., Thompson, Alastair M., and Sen, Subrata

Published
2024
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5. The presentation, management and outcome of patients with ductal carcinoma in situ (DCIS) with microinvasion (invasion ≤1 mm in size)—results from the UK Sloane Project

Author

Shaaban, Abeer M., Hilton, Bridget, Clements, Karen, Dodwell, David, Sharma, Nisha, Kirwan, Cliona, Sawyer, Elinor, Maxwell, Anthony, Wallis, Matthew, Stobart, Hilary, Mylvaganam, Senthurun, Litherland, Janet, Brace-McDonnell, Samantha, Dulson-Cox, Joanne, Kearins, Olive, Provenzano, Elena, Ellis, Ian O., Pinder, Sarah E., and Thompson, Alastair M.

Published
2022
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9. Atypia detected during breast screening and subsequent development of cancer: observational analysis of the Sloane atypia prospective cohort in England

Author

Freeman, Karoline, primary, Jenkinson, David, additional, Clements, Karen, additional, Wallis, Matthew G, additional, Pinder, Sarah E, additional, Provenzano, Elena, additional, Stobart, Hilary, additional, Stallard, Nigel, additional, Kearins, Olive, additional, Sharma, Nisha, additional, Shaaban, Abeer, additional, Kirwan, Cliona Clare, additional, Hilton, Bridget, additional, Thompson, Alastair M, additional, and Taylor-Phillips, Sian, additional

Published
2024
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10. Evidence-informed recommendations on managing breast screening atypia: perspectives from an expert panel consensus meeting reviewing results from the Sloane atypia project

Author

Freeman, Karoline, primary, Mansbridge, Alice, additional, Stobart, Hilary, additional, Clements, Karen, additional, Wallis, Matthew G, additional, Pinder, Sarah E, additional, Kearins, Olive, additional, Shaaban, Abeer M, additional, Kirwan, Cliona C, additional, Wilkinson, Louise S, additional, Webb, Sharon, additional, O’Sullivan, Emma, additional, Jenkins, Jacquie, additional, Wright, Suzanne, additional, Taylor, Kathryn, additional, Bailey, Claire, additional, Holcombe, Chris, additional, Wyld, Lynda, additional, Edwards, Kim, additional, Jenkinson, David J, additional, Sharma, Nisha, additional, Provenzano, Elena, additional, Hilton, Bridget, additional, Stallard, Nigel, additional, Thompson, Alastair M, additional, and Taylor-Phillips, Sian, additional

Published
2023
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11. Development and quality appraisal of a new English breast screening linked data set as part of the age, test threshold, and frequency of mammography screening (ATHENA-M) study

Author

Brettschneider, Julia, primary, Morrison, Breanna, additional, Jenkinson, David, additional, Freeman, Karoline, additional, Walton, Jackie, additional, Sitch, Alice, additional, Hudson, Sue, additional, Kearins, Olive, additional, Mansbridge, Alice, additional, Pinder, Sarah E, additional, Given-Wilson, Rosalind, additional, Wilkinson, Louise, additional, Wallis, Matthew G, additional, Cheung, Shan, additional, and Taylor-Phillips, Sian, additional

Published
2023
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13. Predictors of pathological complete response to neoadjuvant treatment and changes to post-neoadjuvant HER2 status in HER2-positive invasive breast cancer

Author

Katayama, Ayaka, Miligy, Islam M., Shiino, Sho, Toss, Michael S., Eldib, Karim, Kurozumi, Sasagu, Quinn, Cecily M., Badr, Nahla, Murray, Ciara, Provenzano, Elena, Callagy, Grace, Martyn, Cian, Millican-Slater, Rebecca, Purdie, Colin, Purnell, Dave, Pinder, Sarah E., Oyama, Tetsunari, Shaaban, Abeer M., Ellis, Ian, Lee, Andrew H.S., and Rakha, Emad A.

Published
2021
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14. Somatic mutations reveal asymmetric cellular dynamics in the early human embryo.

Author

Ju, Young Seok, Martincorena, Inigo, Gerstung, Moritz, Petljak, Mia, Alexandrov, Ludmil B, Rahbari, Raheleh, Wedge, David C, Davies, Helen R, Ramakrishna, Manasa, Fullam, Anthony, Martin, Sancha, Alder, Christopher, Patel, Nikita, Gamble, Steve, O'Meara, Sarah, Giri, Dilip D, Sauer, Torril, Pinder, Sarah E, Purdie, Colin A, Borg, Åke, Stunnenberg, Henk, van de Vijver, Marc, Tan, Benita KT, Caldas, Carlos, Tutt, Andrew, Ueno, Naoto T, van 't Veer, Laura J, Martens, John WM, Sotiriou, Christos, Knappskog, Stian, Span, Paul N, Lakhani, Sunil R, Eyfjörd, Jórunn Erla, Børresen-Dale, Anne-Lise, Richardson, Andrea, Thompson, Alastair M, Viari, Alain, Hurles, Matthew E, Nik-Zainal, Serena, Campbell, Peter J, and Stratton, Michael R

Subjects
Blood Cells, Humans, Mutagenesis, Cell Lineage, Embryonic Development, Mutation, Mosaicism, Germ-Line Mutation, Genome, Human, Adult, Embryo, Mammalian, Mutation Rate, Embryo, Mammalian, Genome, Human, General Science & Technology
Abstract

Somatic cells acquire mutations throughout the course of an individual's life. Mutations occurring early in embryogenesis are often present in a substantial proportion of, but not all, cells in postnatal humans and thus have particular characteristics and effects. Depending on their location in the genome and the proportion of cells they are present in, these mosaic mutations can cause a wide range of genetic disease syndromes and predispose carriers to cancer. They have a high chance of being transmitted to offspring as de novo germline mutations and, in principle, can provide insights into early human embryonic cell lineages and their contributions to adult tissues. Although it is known that gross chromosomal abnormalities are remarkably common in early human embryos, our understanding of early embryonic somatic mutations is very limited. Here we use whole-genome sequences of normal blood from 241 adults to identify 163 early embryonic mutations. We estimate that approximately three base substitution mutations occur per cell per cell-doubling event in early human embryogenesis and these are mainly attributable to two known mutational signatures. We used the mutations to reconstruct developmental lineages of adult cells and demonstrate that the two daughter cells of many early embryonic cell-doubling events contribute asymmetrically to adult blood at an approximately 2:1 ratio. This study therefore provides insights into the mutation rates, mutational processes and developmental outcomes of cell dynamics that operate during early human embryogenesis.

Published
2017

15. Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases

Author

Rakha, Emad A., Miligy, Islam M., Quinn, Cecily M., Provenzano, Elena, Shaaban, Abeer M., Marchiò, Caterina, Toss, Michael S., Gallagy, Grace, Murray, Ciara, Walshe, Janice, Katayama, Ayaka, Eldib, Karim, Badr, Nahla, Tanchel, Bruce, Millican-Slater, Rebecca, Purdie, Colin, Purnell, Dave, Pinder, Sarah E., Ellis, Ian O., and Lee, Andrew H. S.

Published
2021
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19. Figure 4 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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20. Figure 2 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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21. Supplementary Figure S1 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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22. Table 1 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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23. Supplementary Table S3 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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24. Data from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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25. Figure 3 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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26. Figure 5 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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27. Figure 1 from Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, primary, Parker, Joel S., primary, Hoadley, Katherine A., primary, Quist, Jelmar, primary, Kernaghan, Sarah, primary, Kilburn, Lucy, primary, Salgado, Roberto, primary, Loi, Sherene, primary, Kennedy, Richard D., primary, Roxanis, Ioannis, primary, Gazinska, Patrycja, primary, Pinder, Sarah E., primary, Bliss, Judith, primary, Perou, Charles M., primary, Haider, Syed, primary, Grigoriadis, Anita, primary, Tutt, Andrew, primary, and Cheang, Maggie Chon U., primary

Published
2023
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28. Ductal Carcinoma in Situ

Author

Carter, Stacey A., Pinder, Sarah E., Thompson, Alastair M., Wyld, Lynda, editor, Markopoulos, Christos, editor, Leidenius, Marjut, editor, and Senkus-Konefka, Elżbieta, editor

Published
2018
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30. Management and 5-year outcomes in 9938 women with screen-detected ductal carcinoma in situ: the UK Sloane Project

Author

Thompson, Alastair, Francis, Adele, Sibbering, Mark, Bishop, Hugh, Carpenter, Robert, George, W.D., Lee, Martin, Nicholson, Stewart, Dobson, Hilary, Evans, Andy, Maxwell, Anthony, Wallis, Matthew, Dodwell, David, Sawyer, Elinor, Adlard, Julian, Dewar, John, Ross, Gillian, Wilcox, Maggie, Hanby, Andrew, Pinder, Sarah, Speirs, Valerie, Thomas, Jeremy, Ellis, Ian, Lakhani, Sunil, Macartney, James, Tomlinson, Ian, Cheung, Shan, Lawrence, Gill, Ball, Graham, Clements, Karen, Hilton, Bridget, Kearins, Olive, Wheaton, Margot, Thompson, Alastair M., Pinder, Sarah E., Ball, Graham R., Thomas, Jeremy St J., Maxwell, Anthony J., Wallis, Matthew G., and Dodwell, David J.

Published
2018
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31. Evidence-informed recommendations on managing breast screening atypia: perspectives from an expert panel consensus meeting reviewing results from the Sloane atypia project.

Author

Freeman, Karoline, Mansbridge, Alice, Stobart, Hilary, Clements, Karen, Wallis, Matthew G, Pinder, Sarah E, Kearins, Olive, Shaaban, Abeer M, Kirwan, Cliona C, Wilkinson, Louise S, Webb, Sharon, O'Sullivan, Emma, Jenkins, Jacquie, Wright, Suzanne, Taylor, Kathryn, Bailey, Claire, Holcombe, Chris, Wyld, Lynda, Edwards, Kim, and Jenkinson, David J

Subjects
BREAST, EARLY detection of cancer, EVIDENCE gaps, RESEARCH personnel, DATA integrity, MAMMOGRAMS
Abstract

Evidence-based clinical guidelines are essential to maximize patient benefit and to reduce clinical uncertainty and inconsistency in clinical practice. Gaps in the evidence base can be addressed by data acquired in routine practice. At present, there is no international consensus on management of women diagnosed with atypical lesions in breast screening programmes. Here, we describe how routine NHS breast screening data collected by the Sloane atypia project was used to inform a management pathway that maximizes early detection of cancer and minimizes over-investigation of lesions with uncertain malignant potential. A half-day consensus meeting with 11 clinical experts, 1 representative from Independent Cancer Patients' Voice, 6 representatives from NHS England (NHSE) including from Commissioning, and 2 researchers was held to facilitate discussions of findings from an analysis of the Sloane atypia project. Key considerations of the expert group in terms of the management of women with screen detected atypia were: (1) frequency and purpose of follow-up; (2) communication to patients; (3) generalizability of study results; and (4) workforce challenges. The group concurred that the new evidence does not support annual surveillance mammography for women with atypia, irrespective of type of lesion, or woman's age. Continued data collection is paramount to monitor and audit the change in recommendations. [ABSTRACT FROM AUTHOR]

Published
2024
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32. Development and quality appraisal of a new English breast screening linked data set as part of the age, test threshold, and frequency of mammography screening (ATHENA-M) study.

Author

Brettschneider, Julia, Morrison, Breanna, Jenkinson, David, Freeman, Karoline, Walton, Jackie, Sitch, Alice, Hudson, Sue, Kearins, Olive, Mansbridge, Alice, Pinder, Sarah E, Given-Wilson, Rosalind, Wilkinson, Louise, Wallis, Matthew G, Cheung, Shan, and Taylor-Phillips, Sian

Subjects
BREAST, MEDICAL screening, AGE groups, MAMMOGRAMS, DATA integrity, EARLY detection of cancer
Abstract

Objectives To build a data set capturing the whole breast cancer screening journey from individual breast cancer screening records to outcomes and assess data quality. Methods Routine screening records (invitation, attendance, test results) from all 79 English NHS breast screening centres between January 1, 1988 and March 31, 2018 were linked to cancer registry (cancer characteristics and treatment) and national mortality data. Data quality was assessed using comparability, validity, timeliness, and completeness. Results Screening records were extracted from 76/79 English breast screening centres, 3/79 were not possible due to software issues. Data linkage was successful from 1997 after introduction of a universal identifier for women (NHS number). Prior to 1997 outcome data are incomplete due to linkage issues, reducing validity. Between January 1, 1997 and March 31, 2018, a total of 11 262 730 women were offered screening of whom 9 371 973 attended at least one appointment, with 139 million person-years of follow-up (a median of 12.4 person years for each woman included) with 73 810 breast cancer deaths and 1 111 139 any-cause deaths. Comparability to reference data sets and internal validity were demonstrated. Data completeness was high for core screening variables (>99%) and main cancer outcomes (>95%). Conclusions The ATHENA-M project has created a large high-quality and representative data set of individual women's screening trajectories and outcomes in England from 1997 to 2018, data before 1997 are lower quality. Advances in knowledge This is the most complete data set of English breast screening records and outcomes constructed to date, which can be used to evaluate and optimize screening. [ABSTRACT FROM AUTHOR]

Published
2024
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34. Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727)

Author

Tovey, Holly, primary, Sipos, Orsolya, additional, Parker, Joel S., additional, Hoadley, Katherine A., additional, Quist, Jelmar, additional, Kernaghan, Sarah, additional, Kilburn, Lucy, additional, Salgado, Roberto, additional, Loi, Sherene, additional, Kennedy, Richard D., additional, Roxanis, Ioannis, additional, Gazinska, Patrycja, additional, Pinder, Sarah E., additional, Bliss, Judith, additional, Perou, Charles M., additional, Haider, Syed, additional, Grigoriadis, Anita, additional, Tutt, Andrew, additional, and Cheang, Maggie Chon U., additional

Published
2023
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40. Microcalcification crystallography as a potential marker of DCIS recurrence

Author

Gosling, Sarah B, Arnold, Emily L, Davies, Samantha K, Cross, Hannah, Bouybayoune, Ihssane, Calabrese, Doriana, Nallala, Jayakrupakar, Pinder, Sarah E, Fu, Liping, Lips, Esther H, King, Lorraine, Marks, Jeffrey, Hall, Allison, Grimm, Lars J, Lynch, Thomas, Pinto, Donna, Stobart, Hilary, Hwang, E Shelley, Wesseling, Jelle, Geraki, Kalotina, Stone, Nicholas, Lyburn, Iain D, Greenwood, Charlene, Rogers, Keith D, Grand Challenge PRECISION Consortium, Gosling, Sarah B [0000-0002-7034-6547], Arnold, Emily L [0000-0001-5469-2071], Davies, Samantha K [0000-0002-1819-1904], Cross, Hannah [0000-0002-5339-4432], Bouybayoune, Ihssane [0000-0002-7185-1991], Calabrese, Doriana [0000-0002-3868-9830], Nallala, Jayakrupakar [0000-0002-9473-5782], and Apollo - University of Cambridge Repository

Subjects
Carcinoma, Intraductal, Noninfiltrating, Crystallography, Carcinoma, Ductal, Breast, Tumor Microenvironment, Humans, Calcinosis, Female, Breast Neoplasms, Neoplasm Recurrence, Local
Abstract

Ductal carcinoma in-situ (DCIS) accounts for 20-25% of all new breast cancer diagnoses. DCIS has an uncertain risk of progression to invasive breast cancer and a lack of predictive biomarkers may result in relatively high levels (~ 75%) of overtreatment. To identify unique prognostic biomarkers of invasive progression, crystallographic and chemical features of DCIS microcalcifications have been explored. Samples from patients with at least 5-years of follow up and no known recurrence (174 calcifications in 67 patients) or ipsilateral invasive breast cancer recurrence (179 microcalcifications in 57 patients) were studied. Significant differences were noted between the two groups including whitlockite relative mass, hydroxyapatite and whitlockite crystal maturity and, elementally, sodium to calcium ion ratio. A preliminary predictive model for DCIS to invasive cancer progression was developed from these parameters with an AUC of 0.797. These results provide insights into the differing DCIS tissue microenvironments, and how these impact microcalcification formation.

Published
2023

43. Multiscale deep learning framework captures systemic immune features in lymph nodes predictive of triple negative breast cancer outcome in large‐scale studies

Author

Verghese, Gregory, primary, Li, Mengyuan, additional, Liu, Fangfang, additional, Lohan, Amit, additional, Kurian, Nikhil Cherian, additional, Meena, Swati, additional, Gazinska, Patrycja, additional, Shah, Aekta, additional, Oozeer, Aasiyah, additional, Chan, Terry, additional, Opdam, Mark, additional, Linn, Sabine, additional, Gillett, Cheryl, additional, Alberts, Elena, additional, Hardiman, Thomas, additional, Jones, Samantha, additional, Thavaraj, Selvam, additional, Jones, J Louise, additional, Salgado, Roberto, additional, Pinder, Sarah E, additional, Rane, Swapnil, additional, Sethi, Amit, additional, and Grigoriadis, Anita, additional

Published
2023
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44. Data from RORγt+ Innate Lymphoid Cells Promote Lymph Node Metastasis of Breast Cancers

Author

Irshad, Sheeba, primary, Flores-Borja, Fabian, primary, Lawler, Katherine, primary, Monypenny, James, primary, Evans, Rachel, primary, Male, Victoria, primary, Gordon, Peter, primary, Cheung, Anthony, primary, Gazinska, Patrycja, primary, Noor, Farzana, primary, Wong, Felix, primary, Grigoriadis, Anita, primary, Fruhwirth, Gilbert O., primary, Barber, Paul R., primary, Woodman, Natalie, primary, Patel, Dominic, primary, Rodriguez-Justo, Manuel, primary, Owen, Julie, primary, Martin, Stewart G., primary, Pinder, Sarah E., primary, Gillett, Cheryl E., primary, Poland, Simon P., primary, Ameer-Beg, Simon, primary, McCaughan, Frank, primary, Carlin, Leo M., primary, Hasan, Uzma, primary, Withers, David R., primary, Lane, Peter, primary, Vojnovic, Borivoj, primary, Quezada, Sergio A., primary, Ellis, Paul, primary, Tutt, Andrew N.J., primary, and Ng, Tony, primary

Published
2023
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47. Video S2, Related to Figure 2 from RORγt+ Innate Lymphoid Cells Promote Lymph Node Metastasis of Breast Cancers

Author

Irshad, Sheeba, primary, Flores-Borja, Fabian, primary, Lawler, Katherine, primary, Monypenny, James, primary, Evans, Rachel, primary, Male, Victoria, primary, Gordon, Peter, primary, Cheung, Anthony, primary, Gazinska, Patrycja, primary, Noor, Farzana, primary, Wong, Felix, primary, Grigoriadis, Anita, primary, Fruhwirth, Gilbert O., primary, Barber, Paul R., primary, Woodman, Natalie, primary, Patel, Dominic, primary, Rodriguez-Justo, Manuel, primary, Owen, Julie, primary, Martin, Stewart G., primary, Pinder, Sarah E., primary, Gillett, Cheryl E., primary, Poland, Simon P., primary, Ameer-Beg, Simon, primary, McCaughan, Frank, primary, Carlin, Leo M., primary, Hasan, Uzma, primary, Withers, David R., primary, Lane, Peter, primary, Vojnovic, Borivoj, primary, Quezada, Sergio A., primary, Ellis, Paul, primary, Tutt, Andrew N.J., primary, and Ng, Tony, primary

Published
2023
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50. Supplementary Figures & Tables from RORγt+ Innate Lymphoid Cells Promote Lymph Node Metastasis of Breast Cancers

Author

Irshad, Sheeba, primary, Flores-Borja, Fabian, primary, Lawler, Katherine, primary, Monypenny, James, primary, Evans, Rachel, primary, Male, Victoria, primary, Gordon, Peter, primary, Cheung, Anthony, primary, Gazinska, Patrycja, primary, Noor, Farzana, primary, Wong, Felix, primary, Grigoriadis, Anita, primary, Fruhwirth, Gilbert O., primary, Barber, Paul R., primary, Woodman, Natalie, primary, Patel, Dominic, primary, Rodriguez-Justo, Manuel, primary, Owen, Julie, primary, Martin, Stewart G., primary, Pinder, Sarah E., primary, Gillett, Cheryl E., primary, Poland, Simon P., primary, Ameer-Beg, Simon, primary, McCaughan, Frank, primary, Carlin, Leo M., primary, Hasan, Uzma, primary, Withers, David R., primary, Lane, Peter, primary, Vojnovic, Borivoj, primary, Quezada, Sergio A., primary, Ellis, Paul, primary, Tutt, Andrew N.J., primary, and Ng, Tony, primary

Published
2023
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