Houstek J - Search Results

1

Different restriction fragment pattern of mtDNA indicative of generalized 8993 point mutations in a boy with lactic acidosis.

Klement P, Zeman J, Hansikova H, Houstkova H, Baudysova M, Houstek J. Klement P, et al. Among authors: houstek j. J Inherit Metab Dis. 1994;17(2):249-50. doi: 10.1007/BF00711630. J Inherit Metab Dis. 1994. PMID: 7967485 No abstract available.

2

Altered properties of mitochondrial ATP-synthase in patients with a T-->G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA.

Houstĕk J, Klement P, Hermanská J, Houstková H, Hansíková H, Van den Bogert C, Zeman J. Houstĕk J, et al. Biochim Biophys Acta. 1995 Jun 9;1271(2-3):349-57. doi: 10.1016/0925-4439(95)00063-a. Biochim Biophys Acta. 1995. PMID: 7605802 Free article.

3

Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.

Kaplanová V, Zeman J, Hansíková H, Cerná L, Houst'ková H, Misovicová N, Houstek J. Kaplanová V, et al. Among authors: houstek j. J Neurol Sci. 2004 Aug 30;223(2):149-55. doi: 10.1016/j.jns.2004.05.001. J Neurol Sci. 2004. PMID: 15337616

4

Deficiency of pyruvate dehydrogenase complex in tissues of an eight month old infant.

Hansikova H, Zeman J, Klement P, Technikova-Dobrova Z, Houstkova H, Houstek J, Papa S. Hansikova H, et al. Among authors: houstek j. Biochem Mol Biol Int. 1993 Dec;31(6):1157-66. Biochem Mol Biol Int. 1993. PMID: 8193600

5

Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies.

Houstek J, Klement P, Hermanská J, Antonická H, Houstková H, Stratilová L, Wanders RJ, Zeman J. Houstek J, et al. Prenat Diagn. 1999 Jun;19(6):552-8. doi: 10.1002/(sici)1097-0223(199906)19:6<552::aid-pd588>3.0.co;2-c. Prenat Diagn. 1999. PMID: 10416972

6

A novel deficiency of mitochondrial ATPase of nuclear origin.

Houstek J, Klement P, Floryk D, Antonická H, Hermanská J, Kalous M, Hansíková H, Hout'ková H, Chowdhury SK, Rosipal T, Kmoch S, Stratilová L, Zeman J. Houstek J, et al. Hum Mol Genet. 1999 Oct;8(11):1967-74. doi: 10.1093/hmg/8.11.1967. Hum Mol Genet. 1999. PMID: 10484764

7

Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairment.

Zeman J, Krijt J, Stratilová L, Hansíková H, Wenchich L, Kmoch S, Chrastina P, Houstek J. Zeman J, et al. Among authors: houstek j. J Inherit Metab Dis. 2000 Jun;23(4):371-4. doi: 10.1023/a:1005639516342. J Inherit Metab Dis. 2000. PMID: 10896297 No abstract available.

8

Genetic defects of cytochrome c oxidase assembly.

Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J. Pecina P, et al. Among authors: houstek j. Physiol Res. 2004;53 Suppl 1:S213-23. Physiol Res. 2004. PMID: 15119951 Free article. Review.

9

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome.

Pecina P, Capková M, Chowdhury SK, Drahota Z, Dubot A, Vojtísková A, Hansíková H, Houst'ková H, Zeman J, Godinot C, Houstek J. Pecina P, et al. Among authors: houstek j. Biochim Biophys Acta. 2003 Sep 1;1639(1):53-63. doi: 10.1016/s0925-4439(03)00127-3. Biochim Biophys Acta. 2003. PMID: 12943968 Free article.

10

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

Jesina P, Tesarová M, Fornůsková D, Vojtísková A, Pecina P, Kaplanová V, Hansíková H, Zeman J, Houstek J. Jesina P, et al. Among authors: houstek j. Biochem J. 2004 Nov 1;383(Pt. 3):561-71. doi: 10.1042/BJ20040407. Biochem J. 2004. PMID: 15265003 Free PMC article.

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

420 results

Search Page

Filters