657 results on '"Tsui, Lap-Chee"'
Search Results
2. Severe Acute Respiratory Syndrome Coronavirus-Like Virus in Chinese Horseshoe Bats
3. Human Chromosome 7: DNA Sequence and Biology
4. Molecular Characterization of a Common Fragile Site (FRA7H) on Human Chromosome 7 by the Cloning of a Simian Virus 40 Integration Site
5. Regulation of Meiotic Chromatin Loop Size by Chromosomal Position
6. Type II Citrullinemia (Citrin Deficiency): A Mysterious Disease caused by a Defect of Calcium-Binding Mitochondrial Carrier Protein
7. Genome-Wide Association Study Identifies NRG1 as a Susceptibility Locus for Hirschsprung's Disease
8. Addenda
9. Biochemical and Molecular Genetics of Cystic Fibrosis
10. A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome
11. γ -crystallin Family of the Mouse Lens: Structural and Evolutionary Relationships
12. Phosphatase Inhibitors Activate Normal and Defective CFTR Chloride Channels
13. Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene
14. High-Resolution Mapping of Mammalian Genes by In situ Hybridization to Free Chromatin
15. Identification of the Cystic Fibrosis Gene: Genetic Analysis
16. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
17. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
18. Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker
19. Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results
20. Additional file 1 of Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence
21. Complex two-gene modulation of lung disease severity in children with cystic fibrosis
22. Citrin/Mitochondrial Glycerol-3-phosphate Dehydrogenase Double Knock-out Mice Recapitulate Features of Human Citrin Deficiency
23. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis
24. Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency
25. Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis
26. Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout mice
27. Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice
28. The International HapMap Project
29. Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to Chromosome 16 but is distinct from the lpd (lipid defect) locus
30. Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice
31. The Human Genome Project
32. Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly
33. A Novel Locus of Ectodermal Dysplasia Maps to Chromosome 10q24.32–q25.1
34. Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping
35. Gene structure of the human MET proto-oncogene
36. Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly
37. Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas
38. Chromosomal mapping of the second humanCD8B gene locus
39. Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X
40. Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse
41. Mutations in the Cystic Fibrosis Transmembrane Regulator Gene and In Vivo Transepithelial Potentials
42. Organization of heterologous DNA inserts on the mouse meiotic chromosome core
43. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
44. Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions
45. Mapping the midkine family of developmentally regulated signaling molecules
46. Modes of DAPI banding and simultaneous in situ hybridization
47. Altered expression and deletion of RMO1 in osteosarcoma
48. MADR2 maps to 18q21 and encodes a TGF beta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma
49. Regulation of meiotic chromatin loop size by chromosomal position
50. Characterization of the segmental duplication LCR7-20 in the human genome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.