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Results of search for 'au:"Tesarová, M"', page 1 of 2
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Authors
Bártek, J
Cerna, L
Elleder, M
Hansikova, H
Hansíková, H
Honzik, T
Honzík, T
Houstek, J
Hrbková, K
Klement, P
Magner, M
Mucha, Z
Scheinar, J
Sobek, A
Tesarova, M
Tesarová, M
Tesařová, M
Wenchich, L
Zeman, J
Zát'ura, F
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Adolescent
Adult
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Child, Preschool
DNA, Mitochondrial
Electron Transport Complex IV
Female
Humans
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Mitochondria
Mutation
Oligospermia
Pregnancy
chemistry
complications
diagnosis
etiology
genetics
metabolism
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Your search returned 30 results.
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1.
[The influence of the quality of nitrogen on cellulose decomposition at various soil moisture].
[electronic resource]
by
Tesarová, M
Producer:
19720712
In:
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abt.: Allgemeine, landwirtschaftliche und technische Mikrobiologie
vol. 126
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2.
Ultrastructure of hydathode trichomes of hemiparasitic Rhinanthus alectorolophus and Odontites vernus: how important is their role in physiology and evolution of parasitism in Orobanchaceae?
[electronic resource]
by
Těšitel, J
Tesařová, M
Producer:
20130509
In:
Plant biology (Stuttgart, Germany)
vol. 15
Online resources:
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3.
[The current role of intracytoplasmic single sperm injection (ICSI) in assisted reproduction].
[electronic resource]
by
Sobek, A
Hrbková, K
Tesarová, M
Producer:
19980617
In:
Ceska gynekologie
vol. 62
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4.
[Hereditary leiomyomatosis and renal cell cancer - HLRCC/multiple cutaneous and uterine leimomyomatosis - MCUL].
[electronic resource]
by
Plevová, P
Hladíková, A
Tesařová, M
Producer:
20121016
In:
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti
vol. 25 Suppl
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5.
Analysis of pharmacotherapy of hypertension in out-patients.
[electronic resource]
by
Vlcek, J
Tesarová, M
Fendrich, Z
Producer:
19951030
In:
Pharmacy world & science : PWS
vol. 17
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6.
Biogenesis of eukaryotic cytochrome c oxidase.
[electronic resource]
by
Stiburek, L
Hansikova, H
Tesarova, M
Cerna, L
Zeman, J
Producer:
20070529
In:
Physiological research
vol. 55 Suppl 2
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7.
The developmental changes in mitochondrial DNA content per cell in human cord blood leukocytes during gestation.
[electronic resource]
by
Pejznochová, M
Tesařová, M
Honzík, T
Hansíková, H
Magner, M
Zeman, J
Producer:
20090305
In:
Physiological research
vol. 57
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8.
Non-invasive screening of cytochrome c oxidase deficiency in children using a dipstick immunocapture assay.
[electronic resource]
by
Rodinová, M
Trefilová, E
Honzík, T
Tesařová, M
Zeman, J
Hansíková, H
Producer:
20151001
In:
Folia biologica
vol. 60
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9.
[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families].
[electronic resource]
by
Tesarová, M
Hansíková, H
Hlavatá, A
Klement, P
Houst'ková, H
Houstĕk, J
Zeman, J
Producer:
20021118
In:
Casopis lekaru ceskych
vol. 141
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10.
The phenotypic spectrum of fifty Czech m.3243A>G carriers.
[electronic resource]
by
Dvorakova, V
Kolarova, H
Magner, M
Tesarova, M
Hansikova, H
Zeman, J
Honzik, T
Producer:
20171212
In:
Molecular genetics and metabolism
vol. 118
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11.
Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.
[electronic resource]
by
Wenchich, L
Drahota, Z
Honzík, T
Hansíková, H
Tesarová, M
Zeman, J
Houstek, J
Producer:
20041005
In:
Physiological research
vol. 52
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12.
Analysis of expression profiles of genes involved in F(o)F(1)-ATP synthase biogenesis during perinatal development in rat liver and skeletal muscle.
[electronic resource]
by
Spáčilová, J
Hůlková, M
Hruštincová, A
Čapek, V
Tesařová, M
Hansíková, H
Zeman, J
Producer:
20170403
In:
Physiological research
vol. 65
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13.
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene.
[electronic resource]
by
Vesela, K
Hansikova, H
Tesarova, M
Martasek, P
Elleder, M
Houstek, J
Zeman, J
Producer:
20050104
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 93
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14.
Infertility treatment of men with non-obstructive azoospermia.
[electronic resource]
by
Sobek, A
Hrbková, K
Mucha, Z
Vodicka, J
Tesarová, M
Zát'ura, F
Scheinar, J
Bártek, J
Producer:
19980826
In:
Acta Universitatis Palackianae Olomucensis Facultatis Medicae
vol. 141
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15.
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)].
[electronic resource]
by
Honzík, T
Tesarová, M
Hansíková, H
Krijt, J
Benes, P
Zámecník, J
Wenchich, L
Zeman, J
Producer:
20061109
In:
Casopis lekaru ceskych
vol. 145
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16.
[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report].
[electronic resource]
by
Cesneková, T
Jurecka, T
Skorkovská, K
Tesarová, M
Hanisková, H
Wenchich, L
Zámecník, J
Zeman, J
Producer:
20120222
In:
Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti
vol. 67
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17.
Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.
[electronic resource]
by
Tesarova, M
Hansikova, H
Kytnarova, J
Houstkova, H
Bohm, M
Cerna, L
Zeman, J
Houstek, J
Producer:
20121002
In:
Toxicology mechanisms and methods
vol. 14
Online resources:
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18.
Mitochondrial DNA depletion in Alpers syndrome.
[electronic resource]
by
Tesarova, M
Mayr, J A
Wenchich, L
Hansikova, H
Elleder, M
Blahova, K
Sperl, W
Zeman, J
Producer:
20041130
In:
Neuropediatrics
vol. 35
Online resources:
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19.
Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development.
[electronic resource]
by
Pejznochova, M
Tesarova, M
Hansikova, H
Magner, M
Honzik, T
Vinsova, K
Hajkova, Z
Havlickova, V
Zeman, J
Producer:
20100818
In:
Mitochondrion
vol. 10
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20.
Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiency.
[electronic resource]
by
Szentiványi, K
Hansíková, H
Krijt, J
Vinšová, K
Tesařová, M
Rozsypalová, E
Klement, P
Zeman, J
Honzík, T
Producer:
20120807
In:
Prague medical report
vol. 113
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