30 results on '"Rao, Chunbao"'
Search Results
2. Raised SPINK1 levels play a role in angiogenesis and the transendothelial migration of ALL cells
3. A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct
4. A novel variant in the CDH23 gene is associated with non-syndromic hearing loss in a Chinese family
5. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family
6. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct
7. Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant
8. Microphthalmia-associated transcription factor regulates skin melanoblast migration by repressing the melanoma cell adhesion molecule
9. Regulation of pigmentation by microRNAs: MITF-dependent microRNA-211 targets TGF-β receptor 2
10. A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome
11. A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.
12. Molecular epidemiological and hematological profile of thalassemia in the Dongguan Region of Guangdong Province, Southern China
13. Differential expression of peptides serves as an indicator of IgA nephropathy in pediatric patients
14. A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat‐Wilson syndrome
15. Identification of pathogenic variants ofERLEC1in individuals with Class III malocclusion by exome sequencing
16. A molecular‐beacon‐based asymmetric PCR assay for detecting polymorphisms related to folate metabolism
17. A targeted gene capture next-generation sequencing panel for genetic screening of newborns
18. A novel homozygous initiation codon variant associated with infantile alpha‐Bcrystallinopathy in a Chinese family
19. BVVLS2 overlooked for 3 years in a pediatric patient caused by novel compound heterozygous mutations in SLC52A2 gene
20. Molecular epidemiological and hematological profile of thalassemia in the Dongguan Region of Guangdong Province, Southern China.
21. Identification of pathogenic variants of ERLEC1 in individuals with Class III malocclusion by exome sequencing.
22. Mutational Screening of GLI3, SHH, and SHH ZRS in 78 Chinese Children with Nonsyndromic Polydactyly
23. Regulation of cell proliferation in the retinal pigment epithelium: Differential regulation of the death-associated protein like-1 DAPL1 by alternative MITF splice forms
24. Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese Family
25. Regulation of cell proliferation in the retinal pigment epithelium: Differential regulation of the death‐associated protein like‐1 DAPL1 by alternative MITF splice forms.
26. Microphthalmia-associated transcription factor regulates skin melanoblast migration by repressing the melanoma cell adhesion molecule
27. Regulation of pigmentation by microRNAs: MITF-dependent microRNA-211 targets TGF-βreceptor 2
28. BMP4 is required for the initial expression of MITF in melanocyte precursor differentiation from embryonic stem cells
29. Regulation of pigmentation by micro RNAs: MITF-dependent micro RNA-211 targets TGF- β receptor 2.
30. A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.