Lu JH - Search Results

1

Molecular characterization of tetralogy of fallot within Digeorge critical region of the chromosome 22.

Lu JH, Chung MY, Betau H, Chien HP, Lu JK. Lu JH, et al. Among authors: lu jk. Pediatr Cardiol. 2001 Jul-Aug;22(4):279-84. doi: 10.1007/s002460010230. Pediatr Cardiol. 2001. PMID: 11455393

2

DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.

Wang JL, Chen SJ, Chung MY, Niu DM, Lin CY, Hwang BT, Lu JH. Wang JL, et al. Among authors: lu jh. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 Sep-Oct;38(5):385-9. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997. PMID: 9401184

3

Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletion.

Lu JH, Chung MY, Hwang B, Chien HP. Lu JH, et al. Pediatrics. 1999 Jul;104(1 Pt 1):87-90. doi: 10.1542/peds.104.1.87. Pediatrics. 1999. PMID: 10390265

4

Influence of ventricular septal defect type on surgical results in children with tetralogy of Fallot.

Fu YC, Hwang B, Weng ZC, Lu JH, Chi CS, Meng CC. Fu YC, et al. Among authors: lu jh. Zhonghua Yi Xue Za Zhi (Taipei). 2000 Nov;63(11):792-7. Zhonghua Yi Xue Za Zhi (Taipei). 2000. PMID: 11155754

5

Chromosome 22q11 microdeletion in conotruncal heart defects: clinical presentation, parental origin and de novo mutations.

Chung MY, Lu JH, Chien HP, Hwang B. Chung MY, et al. Among authors: lu jh. Int J Mol Med. 2001 May;7(5):501-5. doi: 10.3892/ijmm.7.5.501. Int J Mol Med. 2001. PMID: 11295111

6

Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.

Lu JH, Chung MY, Hwang B, Chien HP. Lu JH, et al. Pediatr Cardiol. 2001 May-Jun;22(3):260-3. doi: 10.1007/s002460010219. Pediatr Cardiol. 2001. PMID: 11343161

7

Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot.

Chung MY, Lu JH, Weng YY, Hwang B. Chung MY, et al. Among authors: lu jh. J Mol Med (Berl). 2001 Jun;79(5-6):338-42. doi: 10.1007/s001090100213. J Mol Med (Berl). 2001. PMID: 11485030

8

The paracrine effect of exogenous growth hormone alleviates dysmorphogenesis caused by tbx5 deficiency in zebrafish (Danio rerio) embryos.

Tsai TC, Lu JK, Choo SL, Yeh SY, Tang RB, Lee HY, Lu JH. Tsai TC, et al. Among authors: lu jh, lu jk. J Biomed Sci. 2012 Jul 9;19(1):63. doi: 10.1186/1423-0127-19-63. J Biomed Sci. 2012. PMID: 22776023 Free PMC article.

9

Anti-apoptotic effects of IGF-I on mortality and dysmorphogenesis in tbx5-deficient zebrafish embryos.

Tsai TC, Shih CC, Chien HP, Yang AH, Lu JK, Lu JH. Tsai TC, et al. Among authors: lu jh, lu jk. BMC Dev Biol. 2018 Mar 5;18(1):5. doi: 10.1186/s12861-017-0161-1. BMC Dev Biol. 2018. PMID: 29506474 Free PMC article.

10

Pectoral Fin Anomalies in tbx5a Knockdown Zebrafish Embryos Related to the Cascade Effect of N-Cadherin and Extracellular Matrix Formation.

Lu JK, Tsai TC, Lee H, Hsia K, Lin CH, Lu JH. Lu JK, et al. Among authors: lu jh. J Dev Biol. 2019 Jul 12;7(3):15. doi: 10.3390/jdb7030015. J Dev Biol. 2019. PMID: 31336923 Free PMC article.

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