356 results on '"Song, Huai-Dong"'
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2. Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB
3. Lymphocyte infiltration and thyrocyte destruction are driven by stromal and immune cell components in Hashimoto’s thyroiditis
4. TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism
5. Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling
6. Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis
7. Genetic Screening and Functional Analysis of Thyroid Peroxidase Variants in Chinese Patients with Congenital Hypothyroidism.
8. Mutation screening of the TSHR gene in 220 Chinese patients with congenital hypothyroidism
9. Genetic Screening and Functional Analysis of Thyroid Peroxidase Variants in Chinese Patients with Congenital Hypothyroidism
10. Cross-Host Evolution of Severe Acute Respiratory Syndrome Coronavirus in Palm Civet and Human
11. Hematopoietic Gene Expression Profile in Zebrafish Kidney Marrow
12. Influence of two anti-tumor drugs, pazopanib, and axitinib, on the development and thyroid-axis of zebrafish (Danio rerio) embryos/larvae
13. Pathogenic variations inMAML2andMAMLD1contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
14. The isl2a transcription factor regulates pituitary development in zebrafish
15. Large-scale forward genetic screening of zebrafish affecting thyroid development
16. The influence of sunitinib and sorafenib, two tyrosine kinase inhibitors, on development and thyroid system in zebrafish larvae
17. Tpo knockout in zebrafish partially recapitulates clinical manifestations of congenital hypothyroidism and reveals the involvement of TH in proper development of glucose homeostasis
18. Identification of a novel mutation in CYP17A1 gene
19. ITM2A Expands Evidence for Genetic and Environmental Interaction in Graves Disease Pathogenesis
20. Detection of BRAF V600E in Fine-Needle Aspiration Samples of Thyroid Nodules by Droplet Digital PCR
21. Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism
22. Angiotensin-converting enzyme 2 attenuates atherosclerotic lesions by targeting vascular cells
23. Exposure to Fluorene-9-Bisphenol and Bisphenol AF Induces Gonad Injury in Male Zebrafish
24. Thyroid Peroxidase Knockout in Zebrafish Recapitulates the Clinical Manifestations of Congenital Hypothyroidism and Reveals Thyroid Hormone Function to Maintain Glucose Homeostasis
25. Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
26. Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association study
27. The effect of radioiodine treatment on the characteristics of TRAb in Graves’ disease
28. Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects
29. The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women
30. The mutation screening in candidate genes related to thyroid dysgenesis by targeted next‐generation sequencing panel in the Chinese congenital hypothyroidism
31. A five‐gene panel refines differential diagnosis of thyroid nodules
32. Phenotypic Heterogeneity and Fertility Potential of Patients with 17-Hydroxylase/17,20-lyase Deficiency - Supplemental Materials
33. Supplemental Materials.pdf
34. The mechanism of mimecan transcription induced by glucocorticoid in pituitary corticotroph cells
35. Genetic Manipulation on Zebrafish duox Recapitulate the Clinical Manifestations of Congenital Hypothyroidism
36. The expression of mimecan in adrenal tissue plays a role in an organism’s responses to stress
37. Molecular and clinical genetics of the transcription factor GLIS3 in Chinese congenital hypothyroidism
38. Three‐dimensional microscopy and image fusion reconstruction analysis of the thyroid gland during morphogenesis
39. Novel Compound Heterozygous Pathogenic Mutations of SLC5A5 in a Chinese Patient With Congenital Hypothyroidism
40. Interleukin-18 enhances glucose uptake in 3T3-L1 adipocytes
41. Genetic diagnosis of multiple affected tissues in a patient with McCune–Albright syndrome
42. Structure and functional analysis of unclassified genes strongly expressed in human visceral adipose tissue
43. Thyroid Peroxidase Knockout in Zebrafish Recapitulates the Clinical Manifestations of Congenital Hypothyroidism and Reveals Thyroid Hormone Function to Maintain Glucose Homeostasis
44. Urinary Iodine and Genetic Predisposition to Hashimoto's Thyroiditis in a Chinese Han Population: A Case–Control Study
45. Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis
46. Robust evidence for five new Gravesʼ disease risk loci from a staged genome-wide association analysis
47. Dense mapping of IL2RA shows no association with Gravesʼ disease in Chinese Han population
48. An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves’ disease
49. A novel, complex heterozygous mutation within Gsα gene in patient with McCune-albright syndrome
50. Chromosome localization analysis of genes strongly expressed in human visceral adipose tissue
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