Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Diana Ishak"'
Autor:
Rose Wai-Yee Fok, Cheryl Siow Bin Ong, Désirée Lie, Diana Ishak, Si Ming Fung, Wern Ee Tang, Shirley Sun, Helen Smith, Joanne Yuen Yie Ngeow
Publikováno v:
BMC Family Practice, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background Genetic screening (GS), defined as the clinical testing of a population to identify asymptomatic individuals with the aim of providing those identified as high risk with prevention, early treatment, or reproductive options. Geneti
Externí odkaz:
https://doaj.org/article/af364dd311264fd3a3ee8fa108fdc06b
Autor:
Jace Ming Xuan Chia, Zack Zhong Sheng Goh, Zi Yang Chua, Kennedy Yao Yi Ng, Diana Ishak, Si Ming Fung, Joanne Yuen Yie Ngeow, Konstadina Griva
Publikováno v:
BMJ Open, Vol 11, Iss 1 (2021)
Objectives Having to access life-sustaining treatment during the emerging COVID-19 outbreak has placed patients with cancer at an especially vulnerable position notwithstanding their immunocompromised condition. The present study aimed to elucidate c
Externí odkaz:
https://doaj.org/article/8b6edf9345304c01b37a85af750b13f3
Publikováno v:
Journal of Mechanical Engineering. 18:233-245
One of the important airline services that can influence the passengers’ loyalty is the in-flight meal service. In this study, the conceptual design process of new in-flight food delivery and waste collection system is carried out using the standar
Autor:
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
Publikováno v:
BMC Family Practice
BMC Family Practice, Vol 22, Iss 1, Pp 1-10 (2021)
BMC Family Practice, Vol 22, Iss 1, Pp 1-10 (2021)
Background Genetic screening (GS), defined as the clinical testing of a population to identify asymptomatic individuals with the aim of providing those identified as high risk with prevention, early treatment, or reproductive options. Genetic screeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::460dca28f0679c25c8a3d8c709bcdac8
https://hdl.handle.net/10356/153955
https://hdl.handle.net/10356/153955
Autor:
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
Publikováno v:
Familial cancer. 19(4)
Neurofibromatosis type 1 (NF1) is a multisystem disorder caused by germline heterozygous NF1 loss-of-function variants. The NF1 gene encodes neurofibromin, a RAS GTPase-activating protein, which functions by down-regulating RAS/RAF/MAPK-signalling pa
Autor:
Soo-Chin Lee, Weng Khong Lim, Zoe Li Ting Ang, Arun Mouli Kolinjivadi, Diana Ishak, Jianbang Chiang, Sock Hoai Chan, Haresh Sankar, Tarryn Shaw, Jing Xian Teo, Eliza Courtney, Siao Ting Chong, Marie Loh, Hui-Yuan Yeh, Joanne Ngeow, Li Zhou, Shao-Tzu Li
Publikováno v:
International journal of cancerREFERENCES. 148(3)
Identification of ancestry-specific pathogenic variants is imperative for diagnostic, treatment, management and prevention strategies, and to understand penetrance/modifiers on risk. Our study aimed to determine the clinical significance of a recurre
Autor:
Si Ming Fung, Zack Zhong Sheng Goh, Diana Ishak, Zi Yang Chua, Jace Ming Xuan Chia, Joanne Ngeow, Konstadina Griva, Kennedy Yao Yi Ng
Publikováno v:
BMJ Open
BMJ Open, Vol 11, Iss 1 (2021)
BMJ Open, Vol 11, Iss 1 (2021)
ObjectivesHaving to access life-sustaining treatment during the emerging COVID-19 outbreak has placed patients with cancer at an especially vulnerable position notwithstanding their immunocompromised condition. The present study aimed to elucidate ca
Autor:
Tarryn Shaw, Joanne Ngeow, Desiree Lie, Sapna Menon, Eliza Courtney, Shao-Tzu Li, Diana Ishak
Publikováno v:
Psycho-oncology. 27(12)
Objective Malays comprise an Asian cultural group reported to have low breast cancer screening uptake rates and poor cancer outcomes. Little is known about Malay cultural factors influencing beliefs and practice of cancer screening and genetic testin
Publikováno v:
Human Genome Variation, Vol 5, Iss 1, Pp 1-5 (2018)
Human Genome Variation
Human Genome Variation
Pallister-Hall syndrome is a rare autosomal dominant condition that is associated with polydactyly and hypothalamic hamartoma and is caused predominantly by frameshift or nonsense pathogenic variants in the GLI3 gene. The majority of cases are identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01f0a06df2322ab0fde98479ebd9b5a6
https://hdl.handle.net/10356/142078
https://hdl.handle.net/10356/142078
Publikováno v:
IOP Conference Series: Materials Science and Engineering. 152:012040
Increased competition in the commercial air transportation industry has made service quality of the airlines as one of the key competitive measures to attract passengers against their rivals. In-flight services, particularly food delivery and waste c