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1
The effects of Aurora Kinase inhibition on thyroid cancer growth and sensitivity to MAPK-directed therapies
The effects of Aurora Kinase inhibition on thyroid cancer growth and sensitivity to MAPK-directed therapies
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The effects of Aurora Kinase inhibition on thyroid cancer growth and sensitivity to MAPK-directed therapies

Hicks, Hannah M ; Nassar, Veronica L ; Lund, Jane ; Rose, Madison M ; Schweppe, Rebecca E

Cancer biology & therapy, 2024-12, Vol.25 (1), p.2332000-2332000 [Periódico revisado por pares]

United States: Taylor & Francis

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2
KATANIN-mediated microtubule severing is required for MTOC organisation and function in Marchantia polymorpha
KATANIN-mediated microtubule severing is required for MTOC organisation and function in Marchantia polymorpha
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KATANIN-mediated microtubule severing is required for MTOC organisation and function in Marchantia polymorpha

Attrill, Sarah T ; Dolan, Liam

Development (Cambridge), 2024-10, Vol.151 (20) [Periódico revisado por pares]

England: The Company of Biologists Ltd

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3
The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration
The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration
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The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration

Karloski, Eve ; Dudley, Beth ; Diergaarde, Brenda ; Blanco, Amie ; Everett, Jessica N. ; Levinson, Elana ; Rangarajan, Tara ; Stanich, Peter P. ; Childers, Kimberly ; Brown, Sandra ; Drogan, Christine ; Cavestro, Giulia Martina ; Gordon, Kelly ; Singh, Aparajita ; Simeone, Diane M. ; Reich, Hannah ; Kastrinos, Fay ; Zakalik, Dana ; Hampel, Heather ; Pearlman, Rachel ; Gordon, Ora K. ; Kupfer, Sonia S. ; Puzzono, Marta ; Zuppardo, Raffaella Alessia ; Brand, Randall E.

Cancer, 2024-10, Vol.130 (19), p.3297-3304 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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4
Polygenic risk scores for genomics and population screening
Polygenic risk scores for genomics and population screening
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Polygenic risk scores for genomics and population screening

Perrott, Sarah L ; Kar, Siddhartha P

The Lancet (British edition), 2024-09, Vol.404 (10456), p.935-936 [Periódico revisado por pares]

London: Elsevier Ltd

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5
Single-cell chromatin accessibility reveals malignant regulatory programs in primary human cancers
Single-cell chromatin accessibility reveals malignant regulatory programs in primary human cancers
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Single-cell chromatin accessibility reveals malignant regulatory programs in primary human cancers

Sundaram, Laksshman ; Kumar, Arvind ; Zatzman, Matthew ; Salcedo, Adriana ; Ravindra, Neal ; Shams, Shadi ; Louie, Brian H. ; Bagdatli, S. Tansu ; Myers, Matthew A. ; Sarmashghi, Shahab ; Choi, Hyo Young ; Choi, Won-Young ; Yost, Kathryn E. ; Zhao, Yanding ; Granja, Jeffrey M. ; Hinoue, Toshinori ; Hayes, D. Neil ; Cherniack, Andrew ; Felau, Ina ; Choudhry, Hani ; Zenklusen, Jean C. ; Farh, Kyle Kai-How ; McPherson, Andrew ; Curtis, Christina ; Laird, Peter W. ; Corces, M. Ryan ; Chang, Howard Y. ; Greenleaf, William J. ; Demchok, John A. ; Yang, Liming ; Tarnuzzer, Roy ; Caesar-Johnson, Samantha J. ; Wang, Zhining ; Doane, Ashley S. ; Khurana, Ekta ; Castro, Mauro A. A. ; Lazar, Alexander J. ; Broom, Bradley M. ; Weinstein, John N. ; Akbani, Rehan ; Kumar, Shwetha V. ; Raphael, Benjamin J. ; Wong, Christopher K. ; Stuart, Joshua M. ; Safavi, Rojin ; Benz, Christopher C. ; Johnson, Benjamin K. ; Kyi, Cindy ; Shen, Hui

Science (American Association for the Advancement of Science), 2024-09, Vol.385 (6713), p.eadk9217 [Periódico revisado por pares]

Washington: The American Association for the Advancement of Science

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6
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis
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Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis

Grassano, Maurizio ; Canosa, Antonio ; D’Alfonso, Sandra ; Corrado, Lucia ; Brodini, Giorgia ; Koumantakis, Emanuele ; Cugnasco, Paolo ; Manera, Umberto ; Vasta, Rosario ; Palumbo, Francesca ; Mazzini, Letizia ; Gallone, Salvatore ; Moglia, Cristina ; Dewan, Ramita ; Chia, Ruth ; Ding, Jinhui ; Dalgard, Clifton ; Gibbs, Raphael J ; Scholz, Sonja ; Calvo, Andrea ; Traynor, Bryan ; Chio, Adriano

Journal of neurology, neurosurgery and psychiatry, 2024-09, p.jnnp-2024-333998 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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7
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline
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SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline

Wood, Katherine A ; Tong, R Spencer ; Motta, Marialetizia ; Cordeddu, Viviana ; Scimone, Eleanor R ; Bush, Stephen J ; Maxwell, Dale W ; Giannoulatou, Eleni ; Caputo, Viviana ; Traversa, Alice ; Mancini, Cecilia ; Ferrero, Giovanni Battista ; Benedicenti, Francesco ; Grammatico, Paola ; Melis, Daniela ; Steindl, Katharina ; Brunetti-Pierri, Nicola ; Trevisson, Eva ; Wilkie, Andrew OM ; Lin, Angela E ; Cormier-Daire, Valérie ; Twigg, Stephen RF ; Tartaglia, Marco ; Goriely, Anne

Elsevier 2024-09

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8
Adrenal tumours in patients with pathogenic APC mutations: a retrospective study
Adrenal tumours in patients with pathogenic APC mutations: a retrospective study
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Adrenal tumours in patients with pathogenic APC mutations: a retrospective study

Lin, Lyman ; Beshay, Victoria ; Macrae, Finlay

Hereditary cancer in clinical practice, 2024-09, Vol.22 (1), p.1-7, Article 17 [Periódico revisado por pares]

London: BioMed Central

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9
Resolving unsolved whole-genome sequencing data in paediatric neurological disorders: a cohort study
Resolving unsolved whole-genome sequencing data in paediatric neurological disorders: a cohort study
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Resolving unsolved whole-genome sequencing data in paediatric neurological disorders: a cohort study

Chi, Ching-Shiang ; Tsai, Chi-Ren ; Lee, Hsiu-Fen

Archives of disease in childhood, 2024-09, Vol.109 (9), p.730-735 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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10
Diagnostic utility of genetic alterations in distinguishing IDH‐wildtype glioblastoma from lower‐grade gliomas: Insight from next‐generation sequencing analysis of 479 cases
Diagnostic utility of genetic alterations in distinguishing IDH‐wildtype glioblastoma from lower‐grade gliomas: Insight from next‐generation sequencing analysis of 479 cases
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Diagnostic utility of genetic alterations in distinguishing IDH‐wildtype glioblastoma from lower‐grade gliomas: Insight from next‐generation sequencing analysis of 479 cases

Lee, Boram ; Hwang, Soohyun ; Bae, Hyunsik ; Choi, Kyue‐Hee ; Suh, Yeon‐Lim

Brain pathology (Zurich, Switzerland), 2024-09, Vol.34 (5), p.e13234-n/a [Periódico revisado por pares]

Switzerland: John Wiley & Sons, Inc

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