Li CM - Search Results

1

A fluorescence-based high-performance liquid chromatographic assay to determine acid ceramidase activity.

He X, Li CM, Park JH, Dagan A, Gatt S, Schuchman EH. He X, et al. Among authors: li cm. Anal Biochem. 1999 Oct 15;274(2):264-9. doi: 10.1006/abio.1999.4284. Anal Biochem. 1999. PMID: 10527524

2

Cloning and characterization of the full-length cDNA and genomic sequences encoding murine acid ceramidase.

Li CM, Hong SB, Kopal G, He X, Linke T, Hou WS, Koch J, Gatt S, Sandhoff K, Schuchman EH. Li CM, et al. Genomics. 1998 Jun 1;50(2):267-74. doi: 10.1006/geno.1998.5334. Genomics. 1998. PMID: 9653654

3

The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expression.

Li CM, Park JH, He X, Levy B, Chen F, Arai K, Adler DA, Disteche CM, Koch J, Sandhoff K, Schuchman EH. Li CM, et al. Genomics. 1999 Dec 1;62(2):223-31. doi: 10.1006/geno.1999.5940. Genomics. 1999. PMID: 10610716

4

Identification and characterization of the molecular lesion causing mucopolysaccharidosis type I in cats.

He X, Li CM, Simonaro CM, Wan Q, Haskins ME, Desnick RJ, Schuchman EH. He X, et al. Among authors: li cm. Mol Genet Metab. 1999 Jun;67(2):106-12. doi: 10.1006/mgme.1999.2860. Mol Genet Metab. 1999. PMID: 10356309

5

Molecular cloning and characterization of a human cDNA and gene encoding a novel acid ceramidase-like protein.

Hong SB, Li CM, Rhee HJ, Park JH, He X, Levy B, Yoo OJ, Schuchman EH. Hong SB, et al. Among authors: li cm. Genomics. 1999 Dec 1;62(2):232-41. doi: 10.1006/geno.1999.5953. Genomics. 1999. PMID: 10610717

6

Molecular cloning and characterization of a full-length complementary DNA encoding human acid ceramidase. Identification Of the first molecular lesion causing Farber disease.

Koch J, Gärtner S, Li CM, Quintern LE, Bernardo K, Levran O, Schnabel D, Desnick RJ, Schuchman EH, Sandhoff K. Koch J, et al. Among authors: li cm. J Biol Chem. 1996 Dec 20;271(51):33110-5. doi: 10.1074/jbc.271.51.33110. J Biol Chem. 1996. PMID: 8955159 Free article.

7

AAV8-mediated hepatic expression of acid sphingomyelinase corrects the metabolic defect in the visceral organs of a mouse model of Niemann-Pick disease.

Barbon CM, Ziegler RJ, Li C, Armentano D, Cherry M, Desnick RJ, Schuchman EH, Cheng SH. Barbon CM, et al. Among authors: li c. Mol Ther. 2005 Sep;12(3):431-40. doi: 10.1016/j.ymthe.2005.03.011. Mol Ther. 2005. PMID: 16099409 Free article.

8

Correction of the Biochemical and Functional Deficits in Fabry Mice Following AAV8-mediated Hepatic Expression of α-galactosidase A.

Ziegler RJ, Cherry M, Barbon CM, Li C, Bercury SD, Armentano D, Desnick RJ, Cheng SH. Ziegler RJ, et al. Among authors: li c. Mol Ther. 2007 Mar;15(3):492-500. doi: 10.1038/sj.mt.6300066. Epub 2016 Dec 8. Mol Ther. 2007. PMID: 28182896

9

Adenovirus-transduced lung as a portal for delivering alpha-galactosidase A into systemic circulation for Fabry disease.

Li C, Ziegler RJ, Cherry M, Lukason M, Desnick RJ, Yew NS, Cheng SH. Li C, et al. Mol Ther. 2002 Jun;5(6):745-54. doi: 10.1006/mthe.2002.0605. Mol Ther. 2002. PMID: 12027559 Free article.

10

Is it possible to foot reflexology for infants with sensorineural hearing loss?

Ai M, Zhang HH, Feng JB, Li CM, Wang WJ, Hu MD. Ai M, et al. Among authors: li cm. World J Clin Cases. 2025 Jan 16;13(2):94509. doi: 10.12998/wjcc.v13.i2.94509. World J Clin Cases. 2025. PMID: 39823104 Free PMC article.

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