1991 - Fellow, The World Academy of Sciences
1991 - Fellow of the Royal Society, United Kingdom
Genetics, Molecular biology, Cystic fibrosis, Gene and Cystic fibrosis transmembrane conductance regulator are his primary areas of study. His is involved in several facets of Genetics study, as is seen by his studies on Human genome, Segmental duplication, Locus, Chromosome 7 and Gene mapping. His Molecular biology study integrates concerns from other disciplines, such as Positional cloning, In situ hybridization, Somatostatin receptor, Kinase and Gene isoform.
The concepts of his Cystic fibrosis study are interwoven with issues in Endocrinology, Mutation and Polymerase chain reaction. In general Gene, his work in Coding region, Gene expression, Exon and Alternative splicing is often linked to Substitution linking many areas of study. His Cystic fibrosis transmembrane conductance regulator research is multidisciplinary, relying on both Dephosphorylation, Mutation, Phenotype, Frameshift mutation and Chloride channel.
His main research concerns Genetics, Molecular biology, Gene, Cystic fibrosis and Gene mapping. His is involved in several facets of Genetics study, as is seen by his studies on Exon, Locus, Chromosome 7, Genetic marker and Chromosome. His Molecular biology research includes themes of Recombinant DNA, Transfection, DNA, Complementary DNA and Fluorescence in situ hybridization.
In his research on the topic of Cystic fibrosis, Gene mutation is strongly related with Endocrinology. His Cystic fibrosis transmembrane conductance regulator study incorporates themes from Phenotype and Chloride channel. His studies deal with areas such as Gastroenterology and Allele as well as Internal medicine.
His primary areas of study are Genetics, Internal medicine, Cystic fibrosis, Endocrinology and Exon. His Genetics research focuses on Gene, Locus, Segmental duplication, Human genome and Genome. He is interested in Cystic fibrosis transmembrane conductance regulator, which is a branch of Cystic fibrosis.
Lap-Chee Tsui has included themes like Cell culture and Allele in his Endocrinology study. His research integrates issues of RNA splicing and Intron in his study of Exon. The study incorporates disciplines such as Molecular biology and Single-nucleotide polymorphism in addition to Complementary DNA.
His scientific interests lie mostly in Genetics, Cystic fibrosis, Segmental duplication, Human genome and Internal medicine. His Cystic fibrosis research focuses on Cystic fibrosis transmembrane conductance regulator in particular. Lap-Chee Tsui focuses mostly in the field of Segmental duplication, narrowing it down to matters related to Chromosome 22 and, in some cases, DNA sequencing, Chromosome 7, Chromosome 21 and Chromosome 19.
His Human genome study combines topics in areas such as Chromosome regions, Chromosome, Structural variation and Copy-number variation. His work deals with themes such as Heterozygote advantage, Endocrinology, Genotyping and Gastroenterology, which intersect with Internal medicine. His Exon research focuses on Missense mutation and how it connects with Allele.
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Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
L. Schmidt;F.-M. Duh;F. Chen;T. Kishida.
Nature Genetics (1997)
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
Erich Roessler;Elena Belloni;Karin Gaudenz;Philippe Jay.
Nature Genetics (1996)
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene.
P. A. Marsden;H. H. Q. Heng;S. W. Scherer;R. J. Stewart.
Journal of Biological Chemistry (1993)
MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinoma
Kolja Eppert;Stephen W Scherer;Hilmi Ozcelik;Rosa Pirone.
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).
Eitan Kerem;Mary Corey;Bat-sheva Kerem;Johanna Rommens.
The New England Journal of Medicine (1990)
A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11
Brian F. O'Dowd;Michael Heiber;Audrey Chan;Henry H.Q. Heng.
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
Mitchell L. Drumm;Heidi A. Pope;William H. Cliff;Johanna M. Rommens.
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E. Belloni;M. Muenke;E. Roessler;G. Traverso.
Nature Genetics (1996)
High-resolution mapping of mammalian genes by in situ hybridization to free chromatin.
H. H. Q. Heng;J. Squire;Lap-Chee Tsui.
Proceedings of the National Academy of Sciences of the United States of America (1992)
Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development.
R. Mo;A. M. Freer;D. L. Zinyk;M. A. Crackower.
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