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Minjing Zou

Showing results (1-10 of 38) with videos related to

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European Journal of Endocrinology|March 26, 2008
Genotype-phenotype correlation in a family with primary cortisol resistance: possible modulating effect of the ER22/23EK polymorphismHussein Raef, Essa Y Baitei, Minjing Zou, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2006
Clinical case seminar: metastatic follicular thyroid carcinoma arising from congenital goiter as a result of a novel splice donor site mutation in the thyroglobulin geneAli S Alzahrani, Essa Y Baitei, Minjing Zou, et al.
Oncogene|December 21, 2004
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell linesKhaled K Abu-Amero, Ali S Alzahrani, Minjing Zou, et al.
Cancer Gene Therapy|February 22, 2002
Gene therapy of melanoma pulmonary metastasis by intramuscular injection of plasmid DNA encoding tissue inhibitor of metalloproteinases-1Yufei Shi, Ranjit S Parhar, Minjing Zou, et al.
BMC Medical Genetics|July 13, 2018
Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a siblingYılmaz Kor, Minjing Zou, Roua A Al-Rijjal, et al.
Clinical Endocrinology|March 27, 2012
Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1AErdem Durmaz, Minjing Zou, Roua A Al-Rijjal, et al.
Neoplasia (New York, N.Y.)|December 25, 2008
Oncogenic activation of MAP kinase by BRAF pseudogene in thyroid tumorsMinjing Zou, Essa Y Baitei, Ali S Alzahrani, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 30, 2008
Diagnosis by serendipity: Cushing syndrome attributable to cortisol-producing adrenal adenoma as the initial manifestation of multiple endocrine neoplasia type 1 due to a rare splicing site MEN1 gene mutationAli S Alzahrani, Nojoud Al-Khaldi, Yufei Shi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX geneMinjing Zou, Derya Buluş, Roua A Al-Rijjal, et al.
Frontiers in Genetics|December 17, 2020
Molecular Analysis of <i>CYP27B1</i> Mutations in Vitamin D-Dependent Rickets Type 1A: c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing ErrorMinjing Zou, Ayla Guven, Huda A BinEssa, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
European Journal of Endocrinology|March 26, 2008
Genotype-phenotype correlation in a family with primary cortisol resistance: possible modulating effect of the ER22/23EK polymorphismHussein Raef, Essa Y Baitei, Minjing Zou, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2006
Clinical case seminar: metastatic follicular thyroid carcinoma arising from congenital goiter as a result of a novel splice donor site mutation in the thyroglobulin geneAli S Alzahrani, Essa Y Baitei, Minjing Zou, et al.
Oncogene|December 21, 2004
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell linesKhaled K Abu-Amero, Ali S Alzahrani, Minjing Zou, et al.
Cancer Gene Therapy|February 22, 2002
Gene therapy of melanoma pulmonary metastasis by intramuscular injection of plasmid DNA encoding tissue inhibitor of metalloproteinases-1Yufei Shi, Ranjit S Parhar, Minjing Zou, et al.
BMC Medical Genetics|July 13, 2018
Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a siblingYılmaz Kor, Minjing Zou, Roua A Al-Rijjal, et al.
Clinical Endocrinology|March 27, 2012
Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1AErdem Durmaz, Minjing Zou, Roua A Al-Rijjal, et al.
Neoplasia (New York, N.Y.)|December 25, 2008
Oncogenic activation of MAP kinase by BRAF pseudogene in thyroid tumorsMinjing Zou, Essa Y Baitei, Ali S Alzahrani, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 30, 2008
Diagnosis by serendipity: Cushing syndrome attributable to cortisol-producing adrenal adenoma as the initial manifestation of multiple endocrine neoplasia type 1 due to a rare splicing site MEN1 gene mutationAli S Alzahrani, Nojoud Al-Khaldi, Yufei Shi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX geneMinjing Zou, Derya Buluş, Roua A Al-Rijjal, et al.
Frontiers in Genetics|December 17, 2020
Molecular Analysis of <i>CYP27B1</i> Mutations in Vitamin D-Dependent Rickets Type 1A: c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing ErrorMinjing Zou, Ayla Guven, Huda A BinEssa, et al.
Pageof 4