Lee B - Search Results

1

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.

Napierala D, Garcia-Rojas X, Sam K, Wakui K, Chen C, Mendoza-Londono R, Zhou G, Zheng Q, Lee B. Napierala D, et al. Among authors: lee b. Mol Genet Metab. 2005 Sep-Oct;86(1-2):257-68. doi: 10.1016/j.ymgme.2005.07.012. Mol Genet Metab. 2005. PMID: 16140555

2

An integrated approach to the diagnosis and prospective management of partial ornithine transcarbamylase deficiency.

Scaglia F, Zheng Q, O'Brien WE, Henry J, Rosenberger J, Reeds P, Lee B. Scaglia F, et al. Among authors: lee b. Pediatrics. 2002 Jan;109(1):150-2. doi: 10.1542/peds.109.1.150. Pediatrics. 2002. PMID: 11773558

3

Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.

Zheng Q, Zhou G, Morello R, Chen Y, Garcia-Rojas X, Lee B. Zheng Q, et al. Among authors: lee b. J Cell Biol. 2003 Sep 1;162(5):833-42. doi: 10.1083/jcb.200211089. J Cell Biol. 2003. PMID: 12952936 Free PMC article.

4

von Voss-Cherstvoy syndrome with transient thrombocytopenia and normal psychomotor development.

Brunetti-Pierri N, Mendoza-Londono R, Shah MR, Karaviti L, Lee B. Brunetti-Pierri N, et al. Among authors: lee b. Am J Med Genet A. 2004 Apr 30;126A(3):299-302. doi: 10.1002/ajmg.a.20593. Am J Med Genet A. 2004. PMID: 15054846 Review.

5

Toxicity and adaptive immune response to intracellular transgenes delivered by helper-dependent vs. first generation adenoviral vectors.

Mian A, Guenther M, Finegold M, Ng P, Rodgers J, Lee B. Mian A, et al. Among authors: lee b. Mol Genet Metab. 2005 Mar;84(3):278-88. doi: 10.1016/j.ymgme.2004.11.005. Epub 2004 Dec 29. Mol Genet Metab. 2005. PMID: 15694178

6

Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

Mendoza-Londono R, Lammer E, Watson R, Harper J, Hatamochi A, Hatamochi-Hayashi S, Napierala D, Hermanns P, Collins S, Roa BB, Hedge MR, Wakui K, Nguyen D, Stockton DW, Lee B. Mendoza-Londono R, et al. Among authors: lee b. Am J Hum Genet. 2005 Jul;77(1):161-8. doi: 10.1086/431654. Epub 2005 May 27. Am J Hum Genet. 2005. PMID: 15924278 Free PMC article.

7

Dysregulation of chondrogenesis in human cleidocranial dysplasia.

Zheng Q, Sebald E, Zhou G, Chen Y, Wilcox W, Lee B, Krakow D. Zheng Q, et al. Among authors: lee b. Am J Hum Genet. 2005 Aug;77(2):305-12. doi: 10.1086/432261. Epub 2005 Jun 10. Am J Hum Genet. 2005. PMID: 15952089 Free PMC article.

8

Gene therapy for inborn errors of liver metabolism.

Brunetti-Pierri N, Lee B. Brunetti-Pierri N, et al. Among authors: lee b. Mol Genet Metab. 2005 Sep-Oct;86(1-2):13-24. doi: 10.1016/j.ymgme.2005.07.015. Mol Genet Metab. 2005. PMID: 16154372 Review.

9

Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia.

Hermanns P, Bertuch AA, Bertin TK, Dawson B, Schmitt ME, Shaw C, Zabel B, Lee B. Hermanns P, et al. Among authors: lee b. Hum Mol Genet. 2005 Dec 1;14(23):3723-40. doi: 10.1093/hmg/ddi403. Epub 2005 Oct 27. Hum Mol Genet. 2005. PMID: 16254002

10

RMRP mutations in cartilage-hair hypoplasia.

Hermanns P, Tran A, Munivez E, Carter S, Zabel B, Lee B, Leroy JG. Hermanns P, et al. Among authors: lee b. Am J Med Genet A. 2006 Oct 1;140(19):2121-30. doi: 10.1002/ajmg.a.31331. Am J Med Genet A. 2006. PMID: 16838329

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

24,295 results

Search Page

Filters