HomeLiterature Search
Popular searches
Retinoic acid receptor beta variant-related colonic hypoganglionosis.

Foster(KJ),Zhang(SQ),Braddock(SR),Torti(E),C… Am J Med Genet A 2019-00-00

Retinoic acid receptor beta (RARB) variants are heavily linked to pathologies of neural crest cell migration. The purpos...

Methylation of tumour suppressor genes associated with thyroid cancer.

Botezatu(A),Iancu(IV),Plesa(A),Manda(D),Popa… Cancer Biomark 2019-00-00

...RARB methylation, respectively was observed. TSGs promoter hypermethylation is a hallmark of cancer and a test that uses...

Clofarabine‑phytochemical combination exposures in CML cells inhibit DNA methyl…

Kaufman-Szymczyk(A),Majda(K),Szuławska-Mrocz… Mol Med Rep 2019-10-00

...RARB), were estimated using MSRA and qPCR, respectively. The tested TSGs were chosen according to bioinformatical analys...

[Application of GLAD-PCR Assay for Study on DNA Methylation in Regulatory Regio…

Smetannikova(NA),Evdokimov(AA),Netesova(NA),… Zhongguo Fei Ai Za Zhi 2019-00-20

...RARB, RASSF1A, RXRG, SIX6, SKOR1 and TERT genes. The results of DNA samples from 40 cancer and 25 normal lung tissues sh...

The Role of MicroRNAs in Early Chondrogenesis of Human Induced Pluripotent Stem…

Stelcer(E),Kulcenty(K),Rucinski(M),Jopek(K),… Int J Mol Sci 2019-09-05

...RARB, SEMA3C. These results were confirmed by RT-qPCR analysis. This work contributes to a better understanding of the r...

Transcriptome analysis offers a comprehensive illustration of the genetic backg…

Shiba(N),Yoshida(K),Hara(Y),Yamato(G),Shirai… Blood Adv 2019-00-22

...RARB, and RUNX1-FNBP1. In addition, we found rare gene rearrangements, namely, MYB-GATA1, NPM1-MLF1, ETV6-NCOA2, ETV6-ME...

HLA-B27-mediated activation of TNAP phosphatase promotes pathogenic syndesmophy…

Liu(CH),Raj(S),Chen(CH),Hung(KH),Chou(CT),Ch… J Clin Invest 2019-00-02

...RARB)/tissue-nonspecific alkaline phosphatase (TNAP) axis accelerated the mineralization of AS MSCs, which was independe...

A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease.

Chatterjee(S),Chakravarti(A) Hum Mol Genet 2019-00-15

...RARB, GATA2 and SOX10 and other HSCR genes. We now demonstrate, using human and mouse cellular and animal models, that E...

Syndromic chorioretinal coloboma associated with heterozygous de novo RARA muta…

Jakubiuk-Tomaszuk(A),Murcia Pienkowski(V),Zi… Clin Genet 2019-00-00

...RARB and RARG. In humans, RARB defects cause syndromic microphthalmia. So far, no germline pathogenic variants have been...

Urinary DNA methylation biomarkers for prediction of prostate cancer upgrading …

Bakavicius(A),Daniunaite(K),Zukauskaite(K),B… Clin Epigenetics 2019-00-05

...RARB, RASSF1, and GSTP1 in 514 preoperatively collected voided or catheterized urine samples from the single-centre coho...

Previous 10 11 12 13 14 15 16 17 18 Next Vol. 14 / of 40

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]