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Search Results - Leon, Thomas Y.Y
Search Results - Leon, Thomas Y.Y
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Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3
by
Leon, Thomas Y.Y
,
Ngan, Elly S.W
,
Poon, Hiu-Ching
,
So, Man-Ting
,
Lui, Vincent C.H
,
Tam, Paul K.H
,
Garcia-Barcelo, Maria Mercedes
Published in
Journal of pediatric surgery
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TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease
by
Garcia-Barcelo, Mercè
,
Ganster, Raymond W.
,
Lui, Vincent C.H.
,
Leon, Thomas Y.Y.
,
So, Man-Ting
,
Lau, Anson M.F.
,
Fu, Ming
,
Sham, Mai-Har
,
Knight, Joanne
,
Zannini, Maria Stella
,
Sham, Pak C.
,
Tam, Paul K.H.
Published in
Human molecular genetics
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MXD1 regulates the H9N2 and H1N1 influenza A virus–induced chemokine expression and their replications in human macrophage
by
Yim, Howard C. H.
,
Leon, Thomas Y. Y.
,
Li, James C. B.
Published in
Journal of leukocyte biology
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A Germline Mutation (A339V) in Thyroid Transcription Factor-1 (TITF-1/NKX2.1) in Patients With Multinodular Goiter and Papillary Thyroid Carcinoma
by
Ngan, Elly S. W.
,
Lang, Brian H. H.
,
Liu, Tingting
,
Shum, Cathy K. Y.
,
So, Man-Ting
,
Lau, Danny K. C.
,
Leon, Thomas Y. Y.
,
Cherny, Stacey S.
,
Tsai, Sophia Y.
,
Lo, Chung-Yau
,
Khoo, Ui-Soon
,
Tam, Paul K. H.
,
Garcia-Barceló, Maria-Mercè
Published in
JNCI : Journal of the National Cancer Institute
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Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population
by
Cornes, Belinda K
,
Tang, Clara S
,
Leon, Thomas Y Y
,
Hui, Kenneth J W S
,
So, Man-Ting
,
Miao, Xiaoping
,
Cherny, Stacey S
,
Sham, Pak C
,
Tam, Paul K H
,
Garcia-Barcelo, Maria-Merce
Published in
PloS one
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Functional analyses of RET mutations in Chinese hirschsprung disease patients
by
Leon, Thomas Y.Y.
,
So, Man-Ting
,
Lui, Vincent C.H.
,
Hofstra, Robert M.W.
,
Tam, Paul K.H.
,
Ngan, Elly S.W.
,
Garcia-Barceló, Maria-Mercè
Published in
Birth defects research. A Clinical and molecular teratology
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Novel RET mutation produces a truncated ret receptor lacking the intracellular signaling domain in a 3-generation family with hirschsprung disease
by
LUI, Vincent C. H
,
LEON, Thomas Y. Y
,
GARCIA- BARCELO, Maria-Mercedes
,
GANSTER, Raymond W
,
CHEN, Benedict L. S
,
HUTSON, John M
,
TAM, Paul K. H
Published in
Clinical chemistry (Baltimore, Md.)
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Birth Defects Research
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Birth Defects Research. A Clinical And Molecular Teratology
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Clinical Chemistry
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Hum Mol Genet
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Human Molecular Genetics
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Human Molecular Genetics Online/Human Molecular Genetics
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Jnci : Journal Of The National Cancer Institute
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Journal Of Leukocyte Biology
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Journal Of Pediatric Surgery
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Journal Of The National Cancer Institute
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Hirschsprung Disease - Genetics
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Polymorphism, Single Nucleotide
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Proto-Oncogene Proteins C-Ret - Genetics
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Receptor Protein-Tyrosine Kinases - Genetics
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