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heterozygosity
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publication
Variegate porfihyria childhood: compound heterozygosity in protoporhyrinogen oxidase gene
Publikace bez příslušnosti k fakultě
publication
A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumours
2003 |
2. lékařská fakulta
publication
Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes
2001 |
2. lékařská fakulta, Ústřední knihovna
publication
Genome Fractionation and Loss of Heterozygosity in Hybrids and Polyploids: Mechanisms, Consequences for Selection, and Link to Gene Function
2021 |
Přírodovědecká fakulta, Ústřední knihovna
publication
Loss of Heterozygosity and Human Telomerase Reverse Transcriptase (hTERT) Expression in Bronchial Mucosa of Heavy Smokers
2007 |
2. lékařská fakulta
publication
OmniPlex-a new QF-PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population
2008 |
2. lékařská fakulta
publication
Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
2005 |
1. lékařská fakulta, 2. lékařská fakulta, Fakulta tělesné výchovy a sportu
publication
Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes
2016 |
1. lékařská fakulta
publication
Loss of heterozygosity in tumours of carriers of germline TP53 mutations
Publikace bez příslušnosti k fakultě
publication
Effects of heterozygosity and MHC diversity on patterns of extra-pair paternity in the socially monogamous scarlet rosefinch
2015 |
Přírodovědecká fakulta
publication
Prevalence and the role of CCR5Δ32 heterozygosity in disease progression in HIV positive patients in the Czech Republic
2019 |
Ústřední knihovna, 3. lékařská fakulta
publication
Variegate Porphyria in Early Childhood: Compound Heterozygosity in Protoporphyrinogen Oxidase Gene
Publikace bez příslušnosti k fakultě
publication
Mikrosatelitové markery ve studiu nádorů prsu
2004 |
Fakulta tělesné výchovy a sportu
publication
Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease
2000 |
1. lékařská fakulta
publication
Comparative analysis of loss of heterozygosity and expression profi le in normal tissue, DCIS and invasive breast cancer
2011 |
1. lékařská fakulta
publication
Molekulárně genetická analýza polymorfismů a STR lokusů u pacientů s nemalobuněčným karcinomem plic
2009 |
1. lékařská fakulta
publication
The human body odour composites are not more attractive than individual samples
Publikace bez příslušnosti k fakultě
publication
The human body odour composites are not more attractive than individual samples
2013 |
Přírodovědecká fakulta, Fakulta humanitních studií
publication
Human body odour composites are not more attractive than individual samples
2013 |
Přírodovědecká fakulta, Fakulta humanitních studií
publication
Autotetraploids of Vicia cracca show a higher allelic richness in natural populations and a higher seed set after artificial selfing than diploids
2014 |
Přírodovědecká fakulta
publication
Human Body Odour Composites Are Not Perceived More Positively than the Individual Samples
2018 |
Přírodovědecká fakulta
publication
Genetic evidence for parthenogenesis in the small carpenter bee Ceratina dallatoreana (Apidae, Ceratinini) in its native distribution range
2023 |
Přírodovědecká fakulta
publication
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger
1998 |
2. lékařská fakulta
publication
Strong fluctuations in aboveground population size do not limit genetic diversity in populations of an endangered biennial species
2018 |
Přírodovědecká fakulta
publication
Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours
1998 |
2. lékařská fakulta
publication
Identification of two compound heterozygous VPS13A large deletions in chorea-acanthocytosis only by protein and quantitative DNA analysis
2020 |
1. lékařská fakulta
publication
A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio-based exome sequencing: A case report
2023 |
2. lékařská fakulta
publication
Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence-absence variation in protein-coding genes
2023 |
1. lékařská fakulta
publication
Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution
2020 |
1. lékařská fakulta
publication
Lineage diversity and reproductive modes of the<it> Daphnia pulex</it> group in Chinese lakes and reservoirs
2019 |
Přírodovědecká fakulta