Henry H.Q. Heng mainly investigates Molecular biology, Genetics, Gene, Chromatin and Genome. His Molecular biology research is multidisciplinary, incorporating elements of genomic DNA, G protein-coupled receptor, In situ hybridization, Somatostatin receptor and Gene mapping. Genetics is frequently linked to Cell biology in his study.
His Gene study deals with Receptor intersecting with Adenine nucleotide and Nucleotide. His Chromatin study integrates concerns from other disciplines, such as Chromosome and Histone. His Genome study incorporates themes from Genetic heterogeneity and Computational biology.
His primary areas of study are Genetics, Molecular biology, Genome, Gene and Computational biology. His Genetics research focuses on Gene mapping, Chromosome, Chromatin, Karyotype and Gene mutation. His Chromosome research includes themes of Prophase and Cell biology.
His Molecular biology study combines topics in areas such as Nucleic acid sequence, In situ hybridization, Complementary DNA, Pseudogene and Fluorescence in situ hybridization. His Genome research incorporates themes from Evolutionary biology, Cancer and Genome instability. His research in Computational biology intersects with topics in Disease, Inheritance, Genetic heterogeneity, Epigenetics and Cancer genome sequencing.
Henry H.Q. Heng mostly deals with Computational biology, Genome, Genetics, Mechanism and Cancer. His research integrates issues of Cellular adaptation, Gene, Human genetics, Chromothripsis and Disease in his study of Computational biology. A large part of his Gene studies is devoted to Gene mutation.
His studies deal with areas such as Karyotype, Genome instability, Inheritance and Somatic evolution in cancer as well as Genome. His work on Chromosome and Chromosome instability as part of general Genetics research is often related to Theology, thus linking different fields of science. His biological study spans a wide range of topics, including Alternative medicine, Cancer research, Aneuploidy and Oncology.
Genome, Computational biology, Genetics, Mechanism and Inheritance are his primary areas of study. His Genome research is multidisciplinary, incorporating elements of Karyotype, Chromothripsis, Genome instability, Gene mutation and Somatic evolution in cancer. Henry H.Q. Heng has researched Karyotype in several fields, including Transcriptome and Chromosome instability.
As a part of the same scientific study, Henry H.Q. Heng usually deals with the Genome instability, concentrating on Cancer and frequently concerns with Alternative medicine and Oncology. His work on Chromosome and Epigenetics as part of general Genetics research is frequently linked to Stress, thereby connecting diverse disciplines of science. As a member of one scientific family, Henry H.Q. Heng mostly works in the field of Inheritance, focusing on Human genetics and, on occasion, Aneuploidy, Complex adaptive system, Cytogenetics and Identification.
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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)
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.
Gene (1993)
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E. Belloni;M. Muenke;E. Roessler;G. Traverso.
Nature Genetics (1996)
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.
Development (1997)
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)
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria
D. Leclerc;A. Wilson;R. Dumas;C. Gafuik.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Modes of DAPI banding and simultaneous in situ hybridization
Henry H. Q. Heng;Lap-Chee Tsui.
Chromosoma (1993)
Identification and cloning of three novel human G protein-coupled receptor genes GPR52, ΨGPR53 and GPR55: GPR55 is extensively expressed in human brain
Marek Sawzdargo;Tuan Nguyen;Dennis K Lee;Kevin R Lynch.
Molecular Brain Research (1999)
HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor
Audrey H. Wang;Nicholas R. Bertos;Marko Vezmar;Nadine Pelletier.
Molecular and Cellular Biology (1999)
Discovery of three novel G-protein-coupled receptor genes
Brian F. O'Dowd;Tuan Nguyen;Adriano Marchese;Regina Cheng.
Genomics (1998)
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