نتائج البحث - "Diana Ishak"

العلاقة: MOH-000232; MOH-000144; MOH-000248; NRF2016NRF-NSFC001–057; NMRC/CSA-INV/0017/2017; npj Genomic Medicine; Hong, J. H., Chong, S. T., Lee, P.-H., Tan, J., Heng, H. L., Nur Diana Ishak, . . . Ngeow, J. (2020). Functional characterisation guides classification of novel BAP1 germline variants. npj Genomic Medicine, 5(1), 50-. doi:10.1038/s41525-020-00157-6; orcid:0000-0002-2173-9192; orcid:0000-0002-9002-350X; orcid:0000-0003-1514-1124; orcid:0000-0003-1558-3627; https://hdl.handle.net/10356/146677Test; 2-s2.0-85096327255

الإتاحة: https://doi.org/10.1038/s41525-020-00157-6Test
https://hdl.handle.net/10356/146677Test

View record in BASE

النص الكامل

5

دورية أكاديمية

Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation

المؤلفون: Chan, Jason Yongsheng, Toh, Ming Ren, Chong, Siao Ting, Nur Diana Ishak, Kolinjivadi, Arun Mouli, Chan, Sock Hoai, Lee, Elizabeth, Boot, Arnoud, Shao-Tzu, Li, Chew, Min-Hoe, Ngeow, Joanne

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), Institute of Molecular and Cellular Biology, A*STAR

مصطلحات موضوعية: Science::Medicine, Cancer Genetics, Genetics Research

وصف الملف: application/pdf

العلاقة: npj Genomic Medicine; Chan, J. Y., Toh, M. R., Chong, S. T., Nur Diana Ishak, Kolinjivadi, A. M., Chan, S. H., . . . Ngeow, J. (2020). Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation. npj Genomic Medicine, 5(1), 39-. doi:10.1038/s41525-020-00146-9; orcid:0000-0002-4801-3703; orcid:0000-0002-9002-350X; orcid:0000-0002-7717-7416; orcid:0000-0003-1558-3627; https://hdl.handle.net/10356/146678Test; 2-s2.0-85091195244

الإتاحة: https://doi.org/10.1038/s41525-020-00146-9Test
https://hdl.handle.net/10356/146678Test

View record in BASE

النص الكامل

6

Design Selection for New In-Flight Food Delivery and Waste Collection System of Commercial Passenger Transport Aircraft using TOPSIS

المؤلفون: Farah Diana Ishak, Fairuz Izzuddin Romli

المصدر: Journal of Mechanical Engineering. 18:233-245

مصطلحات موضوعية: Mechanical Engineering

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0e9b0051640a4c58186916eaa019e3fbTest
https://doi.org/10.24191/jmeche.v18i3.15429Test

7

How practice setting affects family physicians' views on genetic screening: a qualitative study

المؤلفون: Si Ming Fung, Wern Ee Tang, Rose Wai-Yee Fok, Joanne Ngeow, Diana Ishak, Cheryl Siow Bin Ong, Desiree Lie, Shirley Hsiao-Li Sun, Helen Smith

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), School of Social Sciences, National Cancer Centre Singapore, National University Singapore

المصدر: BMC Family Practice
BMC Family Practice, Vol 22, Iss 1, Pp 1-10 (2021)

مصطلحات موضوعية: medicine.medical_specialty, Medicine (General), media_common.quotation_subject, Family physicians, Population, education, Resistance (psychoanalysis), Literacy, 03 medical and health sciences, 0302 clinical medicine, R5-920, Genetic screening, Relevance (law), Medicine, Humans, Medicine [Science], 030212 general & internal medicine, Genetic Testing, Socioeconomic status, Qualitative Research, Primary Care, media_common, 0303 health sciences, education.field_of_study, Motivation, business.industry, Genetic Screening, Research, 030305 genetics & heredity, Public sector, Physicians, Family, General [Social sciences], Public, Primary care, Private, Family medicine, Attitudes, Family Practice, business, Autonomy, Qualitative research, Specialization

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::460dca28f0679c25c8a3d8c709bcdac8Test
https://hdl.handle.net/10356/153955Test

8

Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1

المؤلفون: Felicia Hui Xian Chin, Joanne Ngeow, Tarryn Shaw, Wen Yee Chay, Shao Tzu Li, Eliza Courtney, Sock Hoai Chan, Diana Ishak, Wai Loong Wong, Adele Wong, Khurshid Merchant

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), Cancer Genetics Services, Division of Medical Oncology, National Cancer Centre Singapore, Department of Pathology and Laboratory, KK Women's and Children's Hospital, KK Gynaecological Cancer Centre

المصدر: Familial cancer. 19(4)

مصطلحات موضوعية: 0301 basic medicine, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Neurofibromatosis 1, Loss of Heterozygosity, 030105 genetics & heredity, Germline, Neurofbromatosis, 03 medical and health sciences, 0302 clinical medicine, Genes, Neurofibromatosis 1, Genetics, Medicine, Humans, Genetic Testing, Allele, Neurofibromatosis, neoplasms, Genetics (clinical), Germ-Line Mutation, Ovarian Neoplasms, biology, business.industry, Biological sciences [Science], Cancer, Middle Aged, Neurofbromin, medicine.disease, Neurofibromin 1, Penetrance, eye diseases, nervous system diseases, Pedigree, Serous fluid, Oncology, 030220 oncology & carcinogenesis, biology.protein, Cancer research, Female, business, Ovarian cancer