Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1→p15.4-Reference-Cited by-同舟云学术

Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1→p15.4

Published:1991-02 Issue:2 Volume:9 Page:229-234
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

da Veiga Pereira Lygia,Desnick Robert J.,Adler David A.,Disteche Christine M.,Schuchman Edward H.

Publisher

Elsevier BV

Subject

Genetics

Reference32 articles.

1. The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick disease;Brady,1966

2. Human acid phosphatase in somatic cell hybrids;Brung;Science,1974

3. Niemann-Pick disease in a poodle dog;Bunza;Vet. Pathol,1979

4. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilm's tumor locus;Call;Cell,1990

5. Neutral sphingomyelinase from human urine;Chatterjee;J. Biol. Chem,1989

Cited by 69 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Integrated Computational Analysis of Physicochemical Features, Biological Properties, Kinase Target Prediction and Biotransformation Pathways in Drug Discovery;International Journal of Pharmacology;2024-06-15

2. Importance to include differential diagnostics for acid sphingomyelinase deficiency (ASMD) in patients suspected to have to Gaucher disease;Molecular Genetics and Metabolism;2023-05

3. Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann–Pick disease types A, B and A/B);Orphanet Journal of Rare Diseases;2023-04-17

4. The Niemann-Pick type diseases – A synopsis of inborn errors in sphingolipid and cholesterol metabolism;Progress in Lipid Research;2023-04

5. Niemann-Pick A/B Disease in a 13-Year-Old Child and Review of the Literature;Open Journal of Pediatrics;2023