Tian H - Search Results

1

[Karyotyping and immunophenotyping analyses of the CD34+ CD38- cells isolated from human umbilical cord blood].

Tian H, Zheng JE, Gong FL, Wang XB, Huang SA, Chen Z. Tian H, et al. Zhonghua Xue Ye Xue Za Zhi. 2005 May;26(5):257-60. Zhonghua Xue Ye Xue Za Zhi. 2005. PMID: 15949281 Chinese.

2

Karyotyping, immunophenotyping, and apoptosis analyses on human hematopoietic precursor cells derived from umbilical cord blood following long-term ex vivo expansion.

Tian H, Huang S, Gong F, Tian L, Chen Z. Tian H, et al. Among authors: tian l. Cancer Genet Cytogenet. 2005 Feb;157(1):33-6. doi: 10.1016/j.cancergencyto.2004.06.003. Cancer Genet Cytogenet. 2005. PMID: 15676144

3

[Proliferation and apoptosis in vitro of umbilical cord blood CD34+CD38- hematopoietic early progenitor cells].

Tian H, Huang SA, Gong FL, Zheng JE, He YL, Yang J, Chen Z. Tian H, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2005 Apr;13(2):229-34. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2005. PMID: 15854282 Chinese.

4

[Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa].

Teng Y, Tian H, Wang H, Hu X, Chen Y, Yang Z, Wang W. Teng Y, et al. Among authors: tian h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):164-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673590 Chinese.

5

Analysis of SRY gene in 8 cases of sex abnormality.

Wang H, Teng Y, Tian H, Tang Y, Chen Y, Yang Z. Wang H, et al. Among authors: tian h. J Huazhong Univ Sci Technolog Med Sci. 2004;24(5):503-6. doi: 10.1007/BF02831121. J Huazhong Univ Sci Technolog Med Sci. 2004. PMID: 15641705

6

Mutation identification in a 5-generation pedigree with autosomal dominant retinitis pigmentosa.

Teng Y, Tian H, Wang H, Hu X, Wang W, Chen Y, Yang Z. Teng Y, et al. Among authors: tian h. J Huazhong Univ Sci Technolog Med Sci. 2003;23(3):242-4, 253. doi: 10.1007/BF02829503. J Huazhong Univ Sci Technolog Med Sci. 2003. PMID: 14526423

7

Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation.

Tian H, Yu H, Fu S, Jin R. Tian H, et al. J Huazhong Univ Sci Technolog Med Sci. 2011 Dec;31(6):834-836. doi: 10.1007/s11596-011-0686-7. Epub 2011 Dec 16. J Huazhong Univ Sci Technolog Med Sci. 2011. PMID: 22173508

8

A rare chromosomal abnormality inherited from the mother in a boy conceived after intracytoplasmic sperm injection: a case report.

Yin L, Tian H, Gu LJ, Ma D, Zhang HW, Zhu GJ. Yin L, et al. Among authors: tian h. J Assist Reprod Genet. 2012 Sep;29(9):917-20. doi: 10.1007/s10815-012-9796-9. Epub 2012 May 24. J Assist Reprod Genet. 2012. PMID: 22622526 Free PMC article. No abstract available.

9

A systematic review of animal and clinical studies on the use of scaffolds for urethral repair.

Qi N, Li WJ, Tian H. Qi N, et al. Among authors: tian h. J Huazhong Univ Sci Technolog Med Sci. 2016 Feb;36(1):111-117. doi: 10.1007/s11596-016-1551-5. Epub 2016 Feb 3. J Huazhong Univ Sci Technolog Med Sci. 2016. PMID: 26838750 Review.

10

Synergistic effects of rare variants of ARHGAP31 and FBLN1 in vitro in terminal transverse limb defects.

Tian H, Chu F, Li Y, Xu M, Li W, Li C. Tian H, et al. Front Genet. 2022 Sep 13;13:946854. doi: 10.3389/fgene.2022.946854. eCollection 2022. Front Genet. 2022. PMID: 36176297 Free PMC article.

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