Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Minjing Zou

Showing results (31-40 of 38) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 38 results.
Cancer Research|March 1, 2017
<i>Cyp24a1</i> Attenuation Limits Progression of <i>Braf<sup>V600E</sup></i> -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAF<sup>V600E</sup> Inhibitor PLX4720Minjing Zou, Essa Y Baitei, Huda A BinEssa, et al.
Clinical Endocrinology|June 2, 2011
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotypeHussein Raef, Minjing Zou, Essa Y Baitei, et al.
Clinical Endocrinology|April 7, 2017
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic ricketsAyla Guven, Roua A Al-Rijjal, Huda A BinEssa, et al.
Clinical Endocrinology|October 25, 2011
Molecular characterization of a novel p.R118C mutation in the insulin receptor gene from patients with severe insulin resistanceAli S Alzahrani, Minjing Zou, Essa Y Baitei, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 7, 2015
KRAS(G12D)-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1Minjing Zou, Essa Y Baitei, Roua A Al-Rijjal, et al.
Molecular Cancer Therapeutics|July 5, 2021
β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAF<sup>V600E</sup>-Driven Thyroid Cancer Animal ModelMinjing Zou, Huda A BinEssa, Yousif H Al-Malki, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2018
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid DyshormonogenesisMinjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.
Plos One|March 6, 2018
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3Sezer Acar, Huda A BinEssa, Korcan Demir, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Cancer Research|March 1, 2017
<i>Cyp24a1</i> Attenuation Limits Progression of <i>Braf<sup>V600E</sup></i> -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAF<sup>V600E</sup> Inhibitor PLX4720Minjing Zou, Essa Y Baitei, Huda A BinEssa, et al.
Clinical Endocrinology|June 2, 2011
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotypeHussein Raef, Minjing Zou, Essa Y Baitei, et al.
Clinical Endocrinology|April 7, 2017
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic ricketsAyla Guven, Roua A Al-Rijjal, Huda A BinEssa, et al.
Clinical Endocrinology|October 25, 2011
Molecular characterization of a novel p.R118C mutation in the insulin receptor gene from patients with severe insulin resistanceAli S Alzahrani, Minjing Zou, Essa Y Baitei, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 7, 2015
KRAS(G12D)-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1Minjing Zou, Essa Y Baitei, Roua A Al-Rijjal, et al.
Molecular Cancer Therapeutics|July 5, 2021
β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAF<sup>V600E</sup>-Driven Thyroid Cancer Animal ModelMinjing Zou, Huda A BinEssa, Yousif H Al-Malki, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2018
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid DyshormonogenesisMinjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.
Plos One|March 6, 2018
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3Sezer Acar, Huda A BinEssa, Korcan Demir, et al.
Pageof 4