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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Syndrome and INSC[original query]
Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia.
Hereditary cancer in clinical practice 2010 3 3 (2): 71-6.
Gardovskis Andris, Irmejs Arvids, Miklasevics Edvins, Borosenko Viktors, Bitina Marianna, Melbarde-Gorkusa Inga, Vanags Andrejs, Kurzawski Grzegorz, Suchy Janina, Górski Bohdan, Gardovskis Jan
MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
Journal of human genetics 2016 Mar .
Zahorakova Daniela, Lelkova Petra, Gregor Vladimir, Magner Martin, Zeman Jiri, Martasek Pav
Single-nucleotide polymorphisms in the genes of CES2, CDA and enzymatic activity of CDA for prediction of the efficacy of capecitabine-containing chemotherapy in patients with metastatic breast cancer.
Pharmacological research 2017 Aug .
Lam Siu W, van der Noort Vincent, van der Straaten Tahar, Honkoop Aafke H, Peters Godefridus J, Guchelaar Henk-Jan, Boven Ep
The FADS1 genotypes modify the effect of linoleic acid-enriched diet on adipose tissue inflammation via pro-inflammatory eicosanoid metabolism.
European journal of nutrition 2022 Jun .
Vaittinen Maija, Lankinen Maria A, Käkelä Pirjo, Ågren Jyrki, Wheelock Craig E, Laakso Markku, Schwab Ursula, Pihlajamäki Jus
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