Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M H, Yong"'
Autor:
Cristina Colomer-Winter, Adeline M H Yong, Kelvin K L Chong, Mark Veleba, Pei Yi Choo, Iris Hanxing Gao, Artur Matysik, Foo Kiong Ho, Swaine L Chen, Kimberly A Kline
Publikováno v:
PLoS Genetics, Vol 20, Iss 8, p e1011071 (2024)
Sortase-assembled pili contribute to virulence in many Gram-positive bacteria. In Enterococcus faecalis, the endocarditis and biofilm-associated pilus (Ebp) is polymerized on the membrane by sortase C (SrtC) and attached to the cell wall by sortase A
Externí odkaz:
https://doaj.org/article/94e93fc96b7446b68e1975cb4094025a
Autor:
M H, Yong, J, Che Hamzah
Publikováno v:
The Medical journal of Malaysia. 75(4)
The aim of this study was to investigate the clinical effectiveness, health related quality of life (HRQoL) and cost effectiveness of selective laser trabeculoplasty (SLT) compared to topical anti-glaucoma medications in step-up treatment of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f5cba6726eb96a77c3947350031bc74
https://pubmed.ncbi.nlm.nih.gov/32723992
https://pubmed.ncbi.nlm.nih.gov/32723992
Autor:
Siok Bian Ng, Leendert H. J. Looijenga, Victor Kwan Min Lee, M H Yong, H. Stoop, S Nadarajah, L A Knight
Publikováno v:
Histopathology. 52:644-646
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::511e29dfcd603bf0d8bc80ee67d9b5ab
https://doi.org/10.1111/j.1365-2559.2008.02988.x
https://doi.org/10.1111/j.1365-2559.2008.02988.x
Akademický článek
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Publikováno v:
Singapore medical journal. 50(11)
Neuroblastoma is the most common extracranial solid tumour in children, accounting for about 5.3 percent of all childhood cancers in Singapore. Several genetic abnormalities have been reported as prognostic markers, including amplification of the MYC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3917b6e9243b81dd243190b44682f6a4
https://pubmed.ncbi.nlm.nih.gov/19960166
https://pubmed.ncbi.nlm.nih.gov/19960166
Publikováno v:
Annals of the Academy of Medicine, Singapore. 26(3)
Williams syndrome first described in 1961 is generally characterised by mental deficiency, gregarious personality, unusual "elfin" facies, supravalvular aortic stenosis and idiopathic infantile hypercalcaemia. Patients with Williams syndrome show a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2518f7a688d6000c496780df10e2738f
https://pubmed.ncbi.nlm.nih.gov/9285033
https://pubmed.ncbi.nlm.nih.gov/9285033
Publikováno v:
Singapore medical journal. 38(2)
This report describes a 5-year 6-month-old Chinese girl with partial monosomy for the long arm of chromosome 22. The karyotype was 46,XX/46,XX,del (22) (q13.2). She presented with global developmental delay. Clinical features include seizures, failur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a4efae58ed4cc9fdd9a75ecae0a2acd2
https://pubmed.ncbi.nlm.nih.gov/9269370
https://pubmed.ncbi.nlm.nih.gov/9269370
Autor:
M, Cuozzo-Davis, M H, Yong, P M, Gilmartin, E, Goyvaerts, C, Kuhlemeier, L, Sarokin, N H, Chua
Publikováno v:
Photochemistry and photobiology. 52(1)
RbcS-3A, the most highly expressed member of the pea multigene family encoding the small subunit of ribulose 1,5-bisphosphate carboxylase, is expressed in a light-dependent and organ-specific manner. In order to further delineate the sequences which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1b58adbf6068f43e8ef78b8c02d32df
https://pubmed.ncbi.nlm.nih.gov/2399285
https://pubmed.ncbi.nlm.nih.gov/2399285
Publikováno v:
Journal of Medical Genetics. 32:994-995
A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08acd2d83f3d10b0eba6ffc266e8bb6
https://doi.org/10.1136/jmg.32.12.994
https://doi.org/10.1136/jmg.32.12.994
Publikováno v:
The EMBO Journal. 7:4035-4044
Nuclear protein factor GT-1 binds to sequence boxes II, III, II* and III* upstream of the light-responsive pea rbcS-3A gene. We have shown previously that box II and box III are required for expression of rbcS-3A when redundant elements upstream of -
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b381b84f4aabcbb8870245a6b4bbd2c7
https://doi.org/10.1002/j.1460-2075.1988.tb03297.x
https://doi.org/10.1002/j.1460-2075.1988.tb03297.x