Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Min-Hwee Yong"'
Autor:
Mei Yoke Chan, Yvonne F. L. Yong, Derrick W. Q. Lian, Zhi Xiong Chen, Enrica E. K. Tan, Michaela S. F. Seng, Sharon Ling, Min Hwee Yong, Prasad Iyer, Yong Chen, Eileen H. Q. Ng, Yong Wei Chua, Esther Hee, Meng Kang Wong, Joyce Ching Mei Lam, Muhammad Fahmy Syed, Mee Hiong Ren, Amos Hong Pheng Loh, Sharon Y.Y. Low, Tony Kiat Hon Lim, Chik Hong Kuick, Kenneth Tou En Chang, Sudhanshi Jain, Sheng Hui Tan, Zhang'e Choo, Shui Yen Soh, Ah Moy Tan, Nurfarhanah Bte Syed Sulaiman
Publikováno v:
Cancer Science
Ex vivo evaluation of personalized models can facilitate individualized treatment selection for patients, and advance the discovery of novel therapeutic options. However, for embryonal malignancies, representative primary cultures have been difficult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9fde4a6da673b06ad27d2e50b075f8b
https://doi.org/10.1111/cas.14610
https://doi.org/10.1111/cas.14610
Autor:
Enrica E K Tan, Mui Li Tan, Chik Hong Kuick, Min Hwee Yong, Sharon Y Y Low, Kenneth T E Chang, Char Loo Tan
Publikováno v:
Neuro-Oncology. 24:i123-i123
INTRODUCTION: The four molecular groups (WNT, SHH, Group 3 and Group 4) in medulloblastoma have been well established for the past decade. New subgroups within the four principal molecular groups have recently been discovered and recognized by WHO cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50a9a74bfb4cd1eafdfd4192477a7b9f
https://doi.org/10.1093/neuonc/noac079.446
https://doi.org/10.1093/neuonc/noac079.446
Autor:
Paula Chiam, Cheryl Jia En Lim, John C. Allen, Kenneth Chang, Min Hwee Yong, Nguan Soon Tan, Thiam Chye Tan, Chee Wai Ku
Fetal genetic aberrations constitute up to 50% of all early miscarriages, with aneuploidies accounting for the majority. Serum progesterone is useful in triaging women presenting with threatened miscarriage, and a low progesterone level has been asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c918c2e9f3d6e39b402b36d9655d5473
https://doi.org/10.21203/rs.3.rs-367747/v1
https://doi.org/10.21203/rs.3.rs-367747/v1
Autor:
Guat Lian Peh, Amos Hong Pheng Loh, Alwin Hwai Liang Loh, Chik Hong Kuick, Shui Yen Soh, Shi Wang, Puay Hoon Tan, Min Hwee Yong, Sharon Ling, Kenneth T E Chang, Derrick W. Q. Lian, Sze Jet Aw
Publikováno v:
Pediatric and Developmental Pathology. 18:297-304
Pathological diagnosis of clear cell sarcoma of the kidney (CCSK) is challenging as it resembles blastemal Wilms tumor (WT) and other pediatric sarcomas, and does not have any distinctive immunophenotype. The YWHAE-FAM22 translocation t(10;17)(q22;p1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9989a7813984138f6230aa297272a9a
https://doi.org/10.2350/14-12-1581-oa.1
https://doi.org/10.2350/14-12-1581-oa.1
Autor:
Chi Kuen Lee, Malcolm Lim, Shui Yen Soh, Diana Lim, Benedict Yan, Sharon Y.Y. Low, Min Hwee Yong, Kenneth Tou En Chang, David C.Y. Low, Chik Hong Kuick
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 23
Medulloblastomas are the most common pediatric malignant primary brain tumor. To our knowledge, there are no known critical and druggable tyrosine kinases in medulloblastomas, precluding the use of established tyrosine kinase inhibitors that have sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59c7f0aa880b719e47f8fdfae6c05a44
https://pubmed.ncbi.nlm.nih.gov/26474502
https://pubmed.ncbi.nlm.nih.gov/26474502
Publikováno v:
Cancer Genetics and Cytogenetics. 104:153-156
A 63-year-old man with chronic myeloid leukemia (CML) was found to have a new complex Philadelphia translocation. All of the bone marrow cells had a rearrangement of a five-way translocation, t(9;22;10;12;1), involving a single chromosome 9. The pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6187d0dc893f4d5dfb73f10d7f11bbcc
https://doi.org/10.1016/s0165-4608(97)00451-2
https://doi.org/10.1016/s0165-4608(97)00451-2
Publikováno v:
American journal of medical genetics. Part A. (7)
We report on a pair of twins with trisomy 12p diagnosed postnatally. The girls were referred for dysmorphism and global developmental delay and have been followed from 10 months of age. They have different levels of mosaicism for both buccal cells an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33f55e461babe5edabaea5ef02b9f4ce
https://pubmed.ncbi.nlm.nih.gov/23686734
https://pubmed.ncbi.nlm.nih.gov/23686734
Publikováno v:
Gene. 517(1)
We describe a boy with a de novo deletion of 15.67 Mb spanning 3q22.1q24. He has bilateral micropthalmia, ptosis, cleft palate, global developmental delay and brain, skeletal and cardiac abnormalities. In addition, he has bilateral inguinal hernia an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e88c61ec62d5a5c646083a2aba3a5390
https://pubmed.ncbi.nlm.nih.gov/23313878
https://pubmed.ncbi.nlm.nih.gov/23313878
Gene expression of TRK neurotrophin receptors in advanced neuroblastomas in Singapore--a pilot study
Autor:
Winnie, Fung, Muhammed Yaser, Hasan, Amos Hong Pheng, Loh, Joyce Horng Yiing, Chua, Min Hwee, Yong, Yong Min, Hwee, Louise, Knight, Wei Sek, Hwang, Hwang Wei, Sek, Mei Yoke, Chan, Chan Mei, Yoke, Wan Tew, Seow, Seow Wan, Tew, Anette S, Jacobsen, Chan Hon, Chui, Chui Chan, Hon
Publikováno v:
Pediatric hematology and oncology. 28(7)
The clinical hallmark of neuroblastoma is heterogeneity. Biologically, ploidy and N-Myc amplification are currently the only 2 features used to define risk group and to determine therapy. Tyrosine kinase neurotrophin receptors (Trks, including TrkA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c17e8319c387349d5cf7f5208265449
https://pubmed.ncbi.nlm.nih.gov/21728718
https://pubmed.ncbi.nlm.nih.gov/21728718
Autor:
Kenneth Kwek, Edward T H Tan, Doreen Tsai Hia Tan, Xing Wei, F. M. Lai, George Seow Heong Yeo, Padma Lata, Min Hwee Yong
Publikováno v:
Fetal diagnosis and therapy. 32(3)
Introduction: The aim of this study is to describe the performance of first trimester screening (FTS) for trisomy 21 using maternal age, serum biochemistry and fetal nuchal translucency (NT) in a single center and to evaluate the effect of nasal bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ba437c9f9eb5d8ba0be124f18ece62
https://pubmed.ncbi.nlm.nih.gov/22710343
https://pubmed.ncbi.nlm.nih.gov/22710343