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Zhonghua Gan Zang Bing Za Zhi = Zhonghua Ganzangbing Zazhi = Chinese Journal of Hepatology
|
April 27, 2005
[Assays and clinical significance for determination of hepatitis B virus covalently closed circular DNA]
Ke-Kai Zhao, Xiao-Hui Liao
World Journal of Gastroenterology
|
February 24, 2025
New classification of gastric polyps: An in-depth analysis and critical evaluation
Xiao-Hui Liao, Ying-Ming Sun, Hong-Bin Chen
Plos One
|
February 12, 2016
Angiotensin II Type 2 Receptor Decreases Transforming Growth Factor-β Type II Receptor Expression and Function in Human Renal Proximal Tubule Cells
Hui-Lin Guo, Xiao-Hui Liao, Qi Liu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Analysis of the PAX8 gene in congenital hypothyroidism caused by different forms of thyroid dysgenesis in a father and daughter
Abdullah Bereket, Xiao-Hui Liao, Turgut Turoglu, et al.
Endocrinology
|
December 12, 2019
Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice
Haruki Fujisawa, Manassawee Korwutthikulrangsri, Jiao Fu, et al.
Research Square
|
July 18, 2023
Role of GLIS3 in thyroid development and in the regulation of gene expression in thyroid specific Glis3KO mice
Hong Soon Kang, Sara A Grimm, Xiao-Hui Liao, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 28, 2024
GLIS3 expression in the thyroid gland in relation to TSH signaling and regulation of gene expression
Hong Soon Kang, Sara A Grimm, Xiao-Hui Liao, et al.
Renal Failure
|
December 25, 2009
Expression of augmenter of liver regeneration in rats with gentamicin-induced acute renal failure and its protective effect on kidney
Xiao-Hui Liao, Ling Zhang, Xiao-Peng Tang, et al.
Endocrinology
|
October 14, 2017
Thyroid Hormone Metabolism Defects in a Mouse Model of SBP2 Deficiency
Jiao Fu, Haruki Fujisawa, Benjamin Follman, et al.
American Journal of Human Genetics
|
December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
Alexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.
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of 11
Search research articles
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Showing results (1-10 of 107) with videos related to
Sort By:
Page
of 11
Zhonghua Gan Zang Bing Za Zhi = Zhonghua Ganzangbing Zazhi = Chinese Journal of Hepatology
|
April 27, 2005
[Assays and clinical significance for determination of hepatitis B virus covalently closed circular DNA]
Ke-Kai Zhao, Xiao-Hui Liao
World Journal of Gastroenterology
|
February 24, 2025
New classification of gastric polyps: An in-depth analysis and critical evaluation
Xiao-Hui Liao, Ying-Ming Sun, Hong-Bin Chen
Plos One
|
February 12, 2016
Angiotensin II Type 2 Receptor Decreases Transforming Growth Factor-β Type II Receptor Expression and Function in Human Renal Proximal Tubule Cells
Hui-Lin Guo, Xiao-Hui Liao, Qi Liu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Analysis of the PAX8 gene in congenital hypothyroidism caused by different forms of thyroid dysgenesis in a father and daughter
Abdullah Bereket, Xiao-Hui Liao, Turgut Turoglu, et al.
Endocrinology
|
December 12, 2019
Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice
Haruki Fujisawa, Manassawee Korwutthikulrangsri, Jiao Fu, et al.
Research Square
|
July 18, 2023
Role of GLIS3 in thyroid development and in the regulation of gene expression in thyroid specific Glis3KO mice
Hong Soon Kang, Sara A Grimm, Xiao-Hui Liao, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 28, 2024
GLIS3 expression in the thyroid gland in relation to TSH signaling and regulation of gene expression
Hong Soon Kang, Sara A Grimm, Xiao-Hui Liao, et al.
Renal Failure
|
December 25, 2009
Expression of augmenter of liver regeneration in rats with gentamicin-induced acute renal failure and its protective effect on kidney
Xiao-Hui Liao, Ling Zhang, Xiao-Peng Tang, et al.
Endocrinology
|
October 14, 2017
Thyroid Hormone Metabolism Defects in a Mouse Model of SBP2 Deficiency
Jiao Fu, Haruki Fujisawa, Benjamin Follman, et al.
American Journal of Human Genetics
|
December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
Alexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.
Page
of 11