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Cancer Research|August 17, 2002
CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3Marina Kochetkova, Olivia L D McKenzie, Anthony J Bais, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2025
Lysosome-dependent nutrient scavenging underlies stress adaptation during epithelial-to-mesenchymal transitionMichal J Nagiec, Paola M Cavaliere, Friederike Dundar, et al.
Cancer Research|May 11, 2017
Noninvasive Interrogation of DLL3 Expression in Metastatic Small Cell Lung CancerSai Kiran Sharma, Jacob Pourat, Dalya Abdel-Atti, et al.
American Journal of Human Genetics|May 10, 2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaMark A Corbett, Michael Schwake, Melanie Bahlo, et al.
BMJ Open|May 6, 2021
Relative effectiveness and safety of pharmacotherapeutic agents for patent ductus arteriosus (PDA) in preterm infants: a protocol for a multicentre comparative effectiveness study (CANRxPDA)Souvik Mitra, Amish Jain, Joseph Y Ting, et al.
Human Mutation|April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityMichael J Field, Raman Kumar, Anna Hackett, et al.
BMC Proceedings|June 25, 2020
Proceedings of the 4th BEAT-PCD Conference and 5th PCD Training SchoolLaura E Gardner, Katie L Horton, Amelia Shoemark, et al.
Neurology|May 26, 2021
Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures PlusSarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
Human Mutation|June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variantsDuyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Biorxiv : the Preprint Server for Biology|January 9, 2026
Anatomical White Matter Tracts Span the Cortical Hierarchy to Support Cognitive DiversityJoëlle Bagautdinova, Golia Shafiei, Audrey C Luo, et al.
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