Li H - Search Results

1

Investigating the Metabolic Model in Preterm Neonates by Tandem Mass Spectrometry: A Cohort Study.

Wang B, Zhang Q, Wang Q, Ma J, Cao X, Chen Y, Pan Y, Li H, Xiang J, Wang T. Wang B, et al. Among authors: li h. Horm Metab Res. 2021 Feb;53(2):112-123. doi: 10.1055/a-1300-2294. Epub 2020 Nov 27. Horm Metab Res. 2021. PMID: 33246344

2

Marginal zone B-cell lymphoma of the pulmonary mucosa-associated lymphoid tissue: A case report.

Li H, Wang T, Wei X, Dang X. Li H, et al. Oncol Lett. 2015 Sep;10(3):1731-1734. doi: 10.3892/ol.2015.3375. Epub 2015 Jun 16. Oncol Lett. 2015. PMID: 26622741 Free PMC article.

3

Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing.

Wang T, Duan C, Shen C, Xiang J, He Q, Ding J, Wen P, Zhang Q, Wang W, Liu M, Li H, Li H, Zhang L. Wang T, et al. Among authors: li h. Mol Cytogenet. 2016 Jan 12;9:3. doi: 10.1186/s13039-016-0213-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 26759606 Free PMC article.

4

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Zhu Q, Chen Y, Dai J, Wang B, Liu M, Wang Y, Tao J, Li H. Zhu Q, et al. Among authors: li h. Transl Pediatr. 2015 Jan;4(1):57-62. doi: 10.3978/j.issn.2224-4336.2015.01.02. Transl Pediatr. 2015. PMID: 26835361 Free PMC article.

5

Single Nucleotide Polymorphisms and Osteoarthritis: An Overview and a Meta-Analysis.

Wang T, Liang Y, Li H, Li H, He Q, Xue Y, Shen C, Zhang C, Xiang J, Ding J, Qiao L, Zheng Q. Wang T, et al. Among authors: li h. Medicine (Baltimore). 2016 Feb;95(7):e2811. doi: 10.1097/MD.0000000000002811. Medicine (Baltimore). 2016. PMID: 26886631 Free PMC article. Review.

6

An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing.

Wang T, He Q, Li H, Ding J, Wen P, Zhang Q, Xiang J, Li Q, Xuan L, Kong L, Mao Y, Zhu Y, Shen J, Liang B, Li H. Wang T, et al. Among authors: li h, li q. PLoS One. 2016 Jul 21;11(7):e0159648. doi: 10.1371/journal.pone.0159648. eCollection 2016. PLoS One. 2016. PMID: 27441628 Free PMC article.

7

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.

Chen Y, Liu Y, Wang B, Mao J, Wang T, Ye K, Ye Y, Cram DS, Li H. Chen Y, et al. Among authors: li h. Prenat Diagn. 2016 Dec;36(13):1233-1241. doi: 10.1002/pd.4962. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27862068

8

Noninvasive Prenatal Screening of Fetal Aneuploidy without Massively Parallel Sequencing.

Xu C, Wang T, Liu C, Li H, Chen X, Zhu H, Chen S, Xin Q, Tao J, Huang L, Jiang Z. Xu C, et al. Among authors: li h. Clin Chem. 2017 Apr;63(4):861-869. doi: 10.1373/clinchem.2016.266247. Epub 2017 Feb 14. Clin Chem. 2017. PMID: 28196921

9

17β-Oestradiol promotes differentiation of human embryonic stem cells into dopamine neurons via cross-talk between insulin-like growth factors-1 and oestrogen receptor β.

Li H, Ding C, Ding ZL, Ling M, Wang T, Wang W, Huang B. Li H, et al. J Cell Mol Med. 2017 Aug;21(8):1605-1618. doi: 10.1111/jcmm.13090. Epub 2017 Feb 28. J Cell Mol Med. 2017. PMID: 28244646 Free PMC article.

10

Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis.

Wang T, Li H, Xiang J, Wei B, Zhang Q, Zhu Q, Liu M, Sun M, Li H. Wang T, et al. Among authors: li h. J Int Med Res. 2017 Apr;45(2):549-555. doi: 10.1177/0300060517691699. Epub 2017 Mar 27. J Int Med Res. 2017. PMID: 28345382 Free PMC article.

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