PubMed (OMIM) for id: 333031

Save citations to file

Email citations

Your saved search

Your RSS Feed

Year	Number of Results
1991	1
1993	1
1994	1
1995	2
2001	1
2002	1
2023	0

Results by year

Page 1

Lon protease preferentially degrades oxidized mitochondrial aconitase by an ATP-stimulated mechanism.

Bota DA, Davies KJ. Bota DA, et al. Nat Cell Biol. 2002 Sep;4(9):674-80. doi: 10.1038/ncb836. Nat Cell Biol. 2002. PMID: 12198491

Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.

Innes AM, Chudley AE, Reed MH, Shuckett EP, Hildes-Ripstein GE, Greenberg CR. Innes AM, et al. Am J Med Genet. 2001 Jul 22;102(1):44-7. doi: 10.1002/1096-8628(20010722)102:1<44::aid-ajmg1410>3.0.co;2-7. Am J Med Genet. 2001. PMID: 11471171 Review.

Toward a cDNA map of the human genome.

Korenberg JR, Chen XN, Adams MD, Venter JC. Korenberg JR, et al. Genomics. 1995 Sep 20;29(2):364-70. doi: 10.1006/geno.1995.9993. Genomics. 1995. PMID: 8666383

A human mitochondrial ATP-dependent protease that is highly homologous to bacterial Lon protease.

Wang N, Gottesman S, Willingham MC, Gottesman MM, Maurizi MR. Wang N, et al. Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11247-51. doi: 10.1073/pnas.90.23.11247. Proc Natl Acad Sci U S A. 1993. PMID: 8248235 Free PMC article.

Cloning and sequence analysis of cDNA for a human homolog of eubacterial ATP-dependent Lon proteases.

Amerik AYu, Petukhova GV, Grigorenko VG, Lykov IP, Yarovoi SV, Lipkin VM, Gorbalenya AE. Amerik AYu, et al. FEBS Lett. 1994 Feb 28;340(1-2):25-8. doi: 10.1016/0014-5793(94)80166-5. FEBS Lett. 1994. PMID: 8119403 Free article.

CODAS syndrome: a new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report.

de Almeida JC, Vargas FR, Barbosa-Neto JG, Llerena JC Jr. de Almeida JC, et al. Am J Med Genet. 1995 Jan 2;55(1):19-20. doi: 10.1002/ajmg.1320550107. Am J Med Genet. 1995. PMID: 7702089

Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome--a case report.

Shebib SM, Reed MH, Shuckett EP, Cross HG, Perry JB, Chudley AE. Shebib SM, et al. Am J Med Genet. 1991 Jul 1;40(1):88-93. doi: 10.1002/ajmg.1320400118. Am J Med Genet. 1991. PMID: 1887855

Page of 1

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

7 results

Results by year