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M

Minjing Zou

King Faisal Specialist Hospital and Research Centre

34H指数
100论文数
2.7K被引数
收录论文 45
发表时间
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SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the diseaseSGK3启动子缺失在迟发型低磷性佝偻病中的作用，可能是该疾病的一种遗传病因。
errOrphanet Journal of Rare Diseases
IF3.5
err2026-03-30
err0
errOAAI
errAhmet Uçar; Najla Albader; Amal Qattan; Huda A. BinEssa; Ebru Mısırlı Özdemir; Mustafa Özdemir; Minjing Zou; Ali S. Alzahrani; Yufei Shi
err分享
err收藏
Genome-wide transcriptome analysis and drug target discovery reveal key genes and pathways in thyroid cancer metastasis
errFRONTIERS IN ENDOCRINOLOGY
IF4.6
err2025-02-10
err0
errOAAI
errZou, Minjing; Qattan, Amal; Al-Alwan, Monther; Ghebeh, Hazem; Binjumah, Naif; Al-Haj, Latifa; Khabar, Khalid S. A.; Altaweel, Abdulmohsen; Almohanna, Falah; Assiri, Abdullah M.; Aboussekhra, Abdelilah; Alzahrani, Ali S.; Shi, Yufei
err分享
err收藏
β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in BrafV600E-driven thyroid cancer cells
errFRONTIERS IN IMMUNOLOGY
IF5.9
err2023-07-06
err0
errOAAI
errZou, Minjing; Al-Yahya, Suhad; Al-Alwan, Monther; BinEssa, Huda A.; Khabar, Khalid S. A.; Almohanna, Falah; Assiri, Abdullah M.; Altaweel, Abdulmohsen; Qattan, Amal; Meyer, Brian F.; Alzahrani, Ali S.; Shi, Yufei
err分享
err收藏
Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism先天性甲状腺功能减退症患者RNA剪接的非规范剪接位点变异的见解
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2021-10-11
err6
errOAAI
errAlbader, Najla; Zou, Minjing; BinEssa, Huda A.; Abdi, Saba; Al-Enezi, Anwar F.; Meyer, Brian F.; Alzahrani, Ali S.; Shi, Yufei
err分享
err收藏
β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model
errMOLECULAR CANCER THERAPEUTICS
IF5.5
err2021-06-17
err9
errOAAI
errZou, Minjing; BinEssa, Huda A.; Al-Malki, Yousif H.; Al-Yahya, Suhad; Al-Alwan, Monther; Al-Jammaz, Ibrahim; Khabar, Khalid S. A.; Almohanna, Falah; Assiri, Abdullah M.; Meyer, Brian F.; Alzahrani, Ali S.; Al-Mohanna, Futwan A.; Shi, Yufei
err分享
err收藏
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2021-02-25
err11
errOAAI
errAl-Zayed, Zayed; Al-Rijjal, Roua A.; Al-Ghofaili, Lamya; BinEssa, Huda A.; Pant, Rajeev; Alrabiah, Anwar; Al-Hussainan, Thamer; Zou, Minjing; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION
errENDOCRINE PRACTICE
IF4.6
err2020-01-01
err3
errOAAI
errDemir, Korcan; Zou, Minjing; Al-Rijjal, Roua A.; BinEssa, Huda; Acar, Sezer; Durmaz, Erdem; Catl, Gonul; Al-Enezi, Anwar F.; Alzahrani, Ali S.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2019-12-10
err10
errOAAI
errCebeci, Ayse Nurcan; Zou, Minjing; BinEssa, Huda A.; Alzahrani, Ali S.; Al-Rijjal, Roua A.; Al-Enezi, Anwar F.; Al-Mohanna, Futwan A.; Cavalier, Etienne; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets
errBONE
IF3.6
err2019-08-01
err27
PREAI
errBinEssa, Huda A.; Zou, Minjing; Al-Enezi, Anwar F.; Alomrani, Basma; Al-Faham, Manar S. A.; Al-Rijjal, Roua A.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2018-03-12
err55
errOAAI
errZou, Minjing; Alzahrani, Ali S.; Al-Odaib, Ali; Alqahtani, Mohammad A.; Babiker, Omer; Al-Rijjal, Roua A.; BinEssa, Huda A.; Kattan, Walaa E.; Al-Enezi, Anwar F.; Al Qarni, Ali; Al-Faham, Manar S. A.; Baitei, Essa Y.; Alsagheir, Afaf; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets
errCLINICAL ENDOCRINOLOGY
IF2.4
err2017-05-11
err31
PREAI
errGuven, Ayla; Al-Rijjal, Roua A.; BinEssa, Huda A.; Dogan, Durmus; Kor, Yilmaz; Zou, Minjing; Kaya, Namik; Alenezi, Anwar F.; Hancili, Suna; Tarim, Omer; Baitei, Essa Y.; Kattan, Walaa E.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Cyp24a1 Attenuation Limits Progression of BrafV600E-Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720
errCANCER RESEARCH
IF16.6
err2017-04-13
err16
errOAAI
errZou, Minjing; Baitei, Essa Y.; BinEssa, Huda A.; Al-Mohanna, Futwan A.; Parhar, Ranjit S.; St-Arnaud, Rene; Kimura, Shioko; Pritchard, Catrin; Alzahrani, Ali S.; Assiri, Abdullah M.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
IL-12 immunotherapy of BrafV600E-induced papillary thyroid cancer in a mouse model
errLABORATORY INVESTIGATION
IF4.2
err2016-01-01
err26
errOAAI
errParhar, Ranjit S.; Zou, Minjing; Al-Mohanna, Futwan A.; Baitei, Essa Y.; Assiri, Abdullah M.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
KRASG12D-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1
errLABORATORY INVESTIGATION
IF4.2
err2015-11-01
err12
errOAAI
errZou, Minjing; Baitei, Essa Y.; Al-Rijjal, Roua A.; Parhar, Ranjit S.; Al-Mohanna, Futwan A.; Kimura, Shioko; Pritchard, Catrin; BinEssa, Huda; Alanazi, Azizah A.; Alzahrani, All S.; Akhtar, Mohammed; Assiri, Abdullah M.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer
errONCOGENE
IF7.3
err2015-10-19
err41
errOAAI
errZou, M.; Baitei, E. Y.; Al-Rijjal, R. A.; Parhar, R. S.; Al-Mohanna, F. A.; Kimura, S.; Pritchard, C.; Binessa, H. A.; Alzahrani, A. S.; Al-Khalaf, H. H.; Hawwari, A.; Akhtar, M.; Assiri, A. M.; Meyer, B. F.; Shi, Y.
err分享
err收藏
Concomitant RAS, RET/PTC, or BRAF Mutations in Advanced Stage of Papillary Thyroid Carcinoma甲状腺乳头状癌晚期合并RAS、RET/PTC或BRAF突变
errTHYROID
IF6.7
err2014-08-01
err100
errOAAI
errZou, Minjing; Baitei, Essa Y.; Alzahrani, Ali S.; BinHumaid, Faisal S.; Alkhafaji, Dania; Al-Rijjal, Roua A.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
The mystery of nm23H1 in thyroid cancer
errJOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
IF3.5
err2014-03-18
err0
PREAI
errShi, Y; Zou, M; Farid, NR
err分享
err收藏
Increased CYP24A1 expression is associated with BRAFV600E mutation and advanced stages in papillary thyroid carcinoma
errCLINICAL ENDOCRINOLOGY
IF2.4
err2014-01-21
err13
PREAI
errZou, Minjing; BinHumaid, Faisal S.; Alzahrani, Ali S.; Baitei, Essa Y.; Al-Mohanna, Futwan A.; Meyer, Brian F.; Shi, Yufei
err分享
err收藏
Novel and de novo PHEX mutations in patients with hypophosphatemic rickets低磷血症性佝偻病患者的新的和从头的PHEX突变
errBONE
IF3.6
err2013-01-01
err44
PREAI
errDurmaz, Erdem; Zou, Minjing; Al-Rijjal, Roua A.; Baitei, Essa Y.; Hammami, Sumaya; Bircan, Iffet; Akcurin, Sema; Meyer, Brian; Shi, Yufei
err分享
err收藏
Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A
errCLINICAL ENDOCRINOLOGY
IF2.4
err2012-08-14
err43
PREAI
errDurmaz, Erdem; Zou, Minjing; Al-Rijjal, Roua A.; Bircan, Iffet; Akcurin, Sema; Meyer, Brian; Shi, Yufei
err分享
err收藏

研究方向

暂时未获取到该数据
合作学者
合作期刊
S
Shioko Kimura
H 指数: 74 · 论文数: 306
É
Étienne Cavalier
H 指数: 64 · 论文数: 1.1K
A
Abdullah M. Assiri
H 指数: 56 · 论文数: 251
R
René St‐Arnaud
H 指数: 51 · 论文数: 205
B
Brian F. Meyer
H 指数: 49 · 论文数: 247
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