Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gare Hoon, Yeo"'
Autor:
Byrappa Venkatesh, Ethylin Wang Jabs, Felicia S.H. Cheah, Christoph Winkler, Gare Hoon Yeo, Samuel S. Chong
Publikováno v:
Development Genes and Evolution. 219:289-300
Four members of the twist gene family (twist1a, 1b, 2, and 3) are found in the zebrafish, and they are thought to have arisen through three rounds of gene duplication, two of which occurred prior to the tetrapod-fish split. Phylogenetic analysis grou
Publikováno v:
Developmental Dynamics. 237:2466-2474
Tol1 is a DNA-based transposable element first identified from an albino mutant medaka fish. It has been demonstrated to function as an efficient gene transfer vector in mammalian cells. We now demonstrate Tol1 germline transgenesis in zebrafish. A c
Publikováno v:
Development Genes and Evolution. 217:783-789
TWIST1 encodes a transcription factor that contains a highly conserved basic helix-loop-helix DNA-binding domain and a WR motif. We have isolated a full-length complementary DNA of the zebrafish ortholog of TWIST1 and determined its genomic organizat
Autor:
Josephine M.S. Lum, Stacey K.H. Tay, Youyou Zhou, Jennifer S.H. Kiing, Samuel S. Chong, Gare Hoon Yeo
Publikováno v:
Clinical Chemistry. 52:1492-1500
Background: Fragile X syndrome (FXS), the most common cause of inherited mental impairment, is most commonly related to hyperexpansion and hypermethylation of a polymorphic CGG trinucleotide repeat in the 5′ untranslated region of the FMR1 gene. So
Autor:
Seo Yi Chng, Kian Chung Ong, Lynette Pei-Chi Shek, Daniel Y.T. Goh, Denise L.M. Goh, Gare Hoon Yeo, Samuel S. Chong, Nicola Ngiam
Publikováno v:
Journal of Cystic Fibrosis. 5(3):159-164
BackgroundLittle is known about the relationship between cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asian patients and severe asthma or idiopathic bronchiectasis. We investigated this potential relationship in the Si
Publikováno v:
Clinical Chemistry. 49:209-218
Background: β-Thalassemia is endemic to many regions in Southeast Asia and India, and Methods: Gap-PCR was used to simultaneously amplify the β-globin gene from genomic DNA and to detect the Δ619bp deletion mutation. Multiplex minisequencing was t
Autor:
Seong Feei, Loh, Peng Cheang, Wong, Boran, Jiang, Gare Hoon, Yeo, Arnold S C, Tan, Ethiraj Balaji, Prasath, Joyce, Mathew, Melinda L H, Chan, Wei Chin, Tan, Mahesh, Choolani, Christine H A, Yap, Samuel S, Chong
Publikováno v:
Singapore medical journal. 53(10)
We aimed to develop and implement a short tandem repeat (STR) polymerase chain reaction alternative to fluorescence in situ hybridisation (FISH) for the preimplantation genetic diagnosis (PGD) of chromosomal translocations.Selected informative STRs l
Autor:
Seong Feei Loh, Melinda L. H. Chan, Wei Chin Tan, Ethiraj B. Prasath, Angela Ho, Sherry S.Y. Ho, Boran Jiang, Mui Nee Lim, Arnold S. C. Tan, Joyce Mathew, Gare Hoon Yeo, Mahesh Choolani, Christine Yap, Samuel S. Chong, Peng Cheang Wong, Wen Wang
Publikováno v:
Reproductive biomedicine online. 21(5)
The high incidence of double-gene deletions in α-thalassaemia increases the risk of having pregnancies with homozygous α(0)-thalassaemia, the cause of the lethal haemoglobin (Hb) Bart's hydrops fetalis syndrome. Preimplantation genetic diagnosis (P
Publikováno v:
SPIE Proceedings.
In this paper, fiber optic spectroscopy is developed to detect and quantify recombinant green (EGFP) and red (DsRED) fluorescent proteins in vitro and in vivo. The bacterial expression vectors carrying the coding regions of EGFP and DsRED were introd
Autor:
Gare Hoon Yeo, Cheah, Felicia S. H., Winkler, Christoph, Jabs, Ethylin Wang, Venkatesh, Byrappa, Chong, Samuel S.
Publikováno v:
Development Genes & Evolution; Jun2009, Vol. 219 Issue 6, p289-300, 12p, 4 Color Photographs, 2 Diagrams, 1 Chart, 1 Graph