158 results on '"Cheng, Ruhong"'
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2. Molecular evolution, diversification, and expression assessment of MADS gene family in Setaria italica, Setaria viridis, and Panicum virgatum
3. Haplotype variation and KASP markers for SiPSY1 – A key gene controlling yellow kernel pigmentation in foxtail millet
4. Structural, functional and mechanistic insights uncover the role of starch in foxtail millet cultivars with different congee-making quality
5. Effects of temperature and microwave on the stability of the blast effector complex APikL2A/sHMA25 as determined by molecular dynamics analyses
6. ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
7. Genetic control and phenotypic characterization of panicle architecture and grain yield-related traits in foxtail millet (Setaria italica)
8. High-depth resequencing of 312 accessions reveals the local adaptation of foxtail millet
9. Factors associated with persistence of early-onset atopic dermatitis up to the age of 12 years: a prospective cohort study in China
10. Nearly Optimal Probabilistic Coverage for Roadside Advertisement Dissemination in Urban VANETs
11. Deep-intronic and frameshift DSG1 variants associated with atypical severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome in a Chinese family
12. Diseases with Underlining Internal Conditions
13. Nearly Optimal Probabilistic Coverage for Roadside Data Dissemination in Urban VANETs
14. Correction to: High‑depth resequencing of 312 accessions reveals the local adaptation of foxtail millet
15. Filaggrin Gene Mutations in Asian Races
16. Effect of the treatment by slightly acidic electrolyzed water on the accumulation of γ-aminobutyric acid in germinated brown millet
17. Effects of temperature and light on the stability of the blast effector complex APikL2A/sHMA25 as determined by molecular dynamic analyses
18. Diseases with Underlining Internal Conditions
19. The temperature and light-dependent molecular dynamic investigation on foxtail millet’s blast effector APikL2A/sHMA25
20. Exploring the SiCCT Gene Family and Its Role in Heading Date in Foxtail Millet
21. The first case of Chinese phacomatosis pigmentokeratotica diagnosed by a missenseHRASmosaicism
22. Expansion of the genotypic and phenotypic spectrum of xeroderma pigmentosum in Chinese population
23. S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome
24. Nearly Optimal Probabilistic Coverage for Roadside Data Dissemination in Urban VANETs
25. Lidocaine inhibits staphylococcal enterotoxin-stimulated activation of peripheral blood mononuclear cells from patients with atopic dermatitis
26. Interactions between FLG mutations and allergens in atopic dermatitis
27. Effects of lidocaine on regulatory T cells in atopic dermatitis
28. Protein Isolates from Raw and Cooked Foxtail Millet Attenuate Development of Type 2 Diabetes in Streptozotocin‐Induced Diabetic Mice
29. Hypoglycemic Effect of Prolamin from Cooked Foxtail Millet (Setaria italic) on Streptozotocin-Induced Diabetic Mice
30. Novel small‐insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis
31. The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra‐Deep Sequence
32. Next‐generation sequencing through multi‐gene panel testing for diagnosis of hereditary ichthyosis in Chinese
33. Ankyloblepharon–ectodermal dysplasia–clefting syndrome misdiagnosed as epidermolysis bullosa and congenital ichthyosiform erythroderma: Case report and review of published work
34. Genetic Diversity and Population Structure of Elite Foxtail Millet [Setaria italica(L.) P. Beauv.] Germplasm in China
35. Online Task Assignment for Crowdsensing in Predictable Mobile Social Networks
36. Clinical profiles of pediatric patients with GPP alone and with different IL36RN genotypes
37. Report of Chinese family with severe dermatitis, multiple allergies and metabolic wasting syndrome caused by novel homozygous desmoglein-1 gene mutation
38. Nagashima-type palmoplantar keratosis in a Chinese Han population
39. Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome
40. Prevalence of Atopic Dermatitis in Chinese Children aged 1–7 ys
41. Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome
42. A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome
43. A novel recombinant lineage’s contribution to the outbreak of coxsackievirus A6-associated hand, foot and mouth disease in Shanghai, China, 2012-2013
44. Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population
45. Genome Sequence of a Novel Recombinant Coxsackievirus A6 Strain from Shanghai, China, 2013
46. Innovation of the New Superior Quality Foxtail Millet [Setaria italica (L.) P.Beauv] Variety-Jigu32 with Characteristics of Stress Resistance, Stable and High Yield and Its Physiological Mechanism
47. Prevalent and Rare Mutations in IL-36RN Gene in Chinese Patients with Generalized Pustular Psoriasis and Psoriasis Vulgaris
48. Three novel mutations in the SLCO2A1 gene in two Chinese families with primary hypertrophic osteoarthropathy
49. Mutations in POFUT1, Encoding Protein O-fucosyltransferase 1, Cause Generalized Dowling-Degos Disease
50. Common FLG Mutation K4671X Not Associated with Atopic Dermatitis in Han Chinese in a Family Association Study
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