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Minjing Zou

Showing results (21-30 of 38) with videos related to

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Thyroid : Official Journal of the American Thyroid Association|May 7, 2014
Concomitant RAS, RET/PTC, or BRAF mutations in advanced stage of papillary thyroid carcinomaMinjing Zou, Essa Y Baitei, Ali S Alzahrani, et al.
Plos One|July 2, 2015
Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1AKorcan Demir, Walaa E Kattan, Minjing Zou, et al.
Bone|May 19, 2019
Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic ricketsHuda A BinEssa, Minjing Zou, Anwar F Al-Enezi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinomaHussein Raef, Roua Al-Rijjal, Sameerah Al-Shehri, et al.
International Journal of Endocrinology|August 13, 2015
A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible CardiomyopathyMohammad A Alqahtani, Ayed A Shati, Minjing Zou, et al.
Orphanet Journal of Rare Diseases|February 26, 2021
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostosesZayed Al-Zayed, Roua A Al-Rijjal, Lamya Al-Ghofaili, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
The Journal of Clinical Endocrinology and Metabolism|December 11, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic RicketsAyşe Nurcan Cebeci, Minjing Zou, Huda A BinEssa, et al.
Frontiers in Endocrinology|February 25, 2025
Genome-wide transcriptome analysis and drug target discovery reveal key genes and pathways in thyroid cancer metastasisMinjing Zou, Amal Qattan, Monther Al-Alwan, et al.
Frontiers in Immunology|July 24, 2023
β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in <i>Braf</i>-driven thyroid cancer cellsMinjing Zou, Suhad Al-Yahya, Monther Al-Alwan, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Thyroid : Official Journal of the American Thyroid Association|May 7, 2014
Concomitant RAS, RET/PTC, or BRAF mutations in advanced stage of papillary thyroid carcinomaMinjing Zou, Essa Y Baitei, Ali S Alzahrani, et al.
Plos One|July 2, 2015
Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1AKorcan Demir, Walaa E Kattan, Minjing Zou, et al.
Bone|May 19, 2019
Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic ricketsHuda A BinEssa, Minjing Zou, Anwar F Al-Enezi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinomaHussein Raef, Roua Al-Rijjal, Sameerah Al-Shehri, et al.
International Journal of Endocrinology|August 13, 2015
A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible CardiomyopathyMohammad A Alqahtani, Ayed A Shati, Minjing Zou, et al.
Orphanet Journal of Rare Diseases|February 26, 2021
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostosesZayed Al-Zayed, Roua A Al-Rijjal, Lamya Al-Ghofaili, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
The Journal of Clinical Endocrinology and Metabolism|December 11, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic RicketsAyşe Nurcan Cebeci, Minjing Zou, Huda A BinEssa, et al.
Frontiers in Endocrinology|February 25, 2025
Genome-wide transcriptome analysis and drug target discovery reveal key genes and pathways in thyroid cancer metastasisMinjing Zou, Amal Qattan, Monther Al-Alwan, et al.
Frontiers in Immunology|July 24, 2023
β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in <i>Braf</i>-driven thyroid cancer cellsMinjing Zou, Suhad Al-Yahya, Monther Al-Alwan, et al.
Pageof 4