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Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients
Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients...
EB - Genetika a molekulární biologie
- 2007 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
IDH2 mutations in patients with acute myeloid leukemia: missense p.R140 mutations are linked to disease status
IDH2 mutations in patients with acute myeloid leukemia: missense p.R140 mutations are linked to disease status, without abstract - IDH2 mutations in patients with acute myeloid leukemia: missense p.R140 mutations a...
FD - Onkologie a hematologie
- 2010 •
- Jx •
- Link
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Výsledek na webu
Common CYP21 gene mutations in Czech patients and statistical analysis of worldwide mutation distribution
Common CYP21 gene mutations in Czech patients and statistical analysis of worldwide mutation distribution...
CE - Biochemie
- 2003 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Initial Mutations of Celtic Languages as a Sandhi Phenomenon?
Taking Irish and Welsh as an example, this contribution illustrates possible relationship between mutations and sandhi changes in Celtic languages....
AI - Jazykověda
- 2010 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms...
EB - Genetika a molekulární biologie
- 2007 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
TP53 mutation profile in chronic lymphocytic lekemia: evidence for a disease specific profile from a comprehensive analysis of 268 mutations
The TP53 mutation profile in chronic lymphocytic leukemia (CLL) and the correlation of TP53 mutations with allele status or associated molecular genetics are currently unknown. We performed a large mutation analysis of TP53...
FD - Onkologie a hematologie
- 2010 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Mutation of Saccharomyces cerevisiae that suppress the dominat RAS2 Vall9 mutation.
Mutation of Saccharomyces cerevisiae that suppress the dominat RAS2 Vall9 mutation.
EE - Mikrobiologie, virologie
- 2001 •
- D
Rok uplatnění
D - Stať ve sborníku
TP53 mutation profile in chronic lymphocytic leukemia: evidence for a disease specific profile from a comprehensive analysis of 268 mutations
The TP53 mutation profile in chronic lymphocytic leukemia (CLL) and the correlation of TP53 mutations with allele status or associated molecular genetics are currently unknown. We performed a large mutation analysis of TP53...
FD - Onkologie a hematologie
- 2010 •
- Jx •
- Link
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Výsledek na webu
Is screening for hereditary thrombophilia indicated in first early pregnancy loss?
for thrombophilic mutations after the first early pregnancy loss. Thrombophilic mutations were of factor V and II mutation of 9% and 3%, respectively. Single MTHFR mutation was found in 59% and double heterozygous...
FK - Gynekologie a porodnictví
- 2012 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Non-small cell lung cancer with EGFR mutations
mutations in the epidermal growth factor receptor (EGFR) gene and their effect on the sensitivity to the treatment of tyrosine kinase inhibitors (TKI) is known. Mutations occur mutations of EGFR are concentrated. The so-ca...
Respiratory systems
- 2018 •
- Jost
Rok uplatnění
Jost - Ostatní články v recenzovaných periodicích
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