المؤلفون: Giliazova Ir, Khidiiatova, Popova Sn, Elza Khusnutdinova, Slominskiĭ Pa, Limborskaia Sa, R. V. Magzhanov, Miloserdova Ov

المصدر: Russian Journal of Genetics. 39:166-171

مصطلحات موضوعية: Genetics, Heterozygote advantage, Disease, Biology, Idiopathic parkinson's disease, Molecular biology, Human genetics, law.invention, Exon, law, DNA Mutational Analysis, Gene, Polymerase chain reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7c4b83cc18f234f32135611e64a78de1
https://doi.org/10.1023/a:1022427708736

المؤلفون: Akhmadishina LZ, Giliazova IR, Kutlyeva LR, Korytina GF, Kochetova OV, Urmantsev MF, Izmaĭlova SM, Izmaĭlov AA, Kunsbaeva GB, Zagidullin AA, Haliullin AA, Pavlov VN, Viktorova TV, Husnutdinova EK

المصدر: Genetika [Genetika] 2014 Apr; Vol. 50 (4), pp. 481-90.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Izdatelstvo Nauka Country of Publication: Russia (Federation) NLM ID: 0047354 Publication Model: Print Cited Medium: Print ISSN: 0016-6758 (Print) Linking ISSN: 00166758 NLM ISO Abbreviation: Genetika Subsets: MEDLINE

مواضيع طبية MeSH: Carcinoma, Renal Cell/*genetics , DNA-Binding Proteins/*genetics , Urinary Bladder Neoplasms/*genetics , Xeroderma Pigmentosum Group D Protein/*genetics, Aged ; Asian People ; Carcinoma, Renal Cell/pathology ; Disease Progression ; Ethnicity/genetics ; Female ; Genetic Association Studies ; Humans ; Male ; Middle Aged ; Neoplasm Staging ; Polymorphism, Single Nucleotide ; Urinary Bladder Neoplasms/pathology ; X-ray Repair Cross Complementing Protein 1

المؤلفون: Goncharova OV, Bermisheva MA, Giliazova IR, Lipatov ON, Khusnutdinova EK

المصدر: Voprosy onkologii [Vopr Onkol] 2009; Vol. 55 (2), pp. 151-7.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Nauchno-issledovatelʹskiĭ institut onkologii im. N.N. Petrova Country of Publication: Russia (Federation) NLM ID: 0413775 Publication Model: Print Cited Medium: Print ISSN: 0507-3758 (Print) Linking ISSN: 05073758 NLM ISO Abbreviation: Vopr Onkol Subsets: MEDLINE

مواضيع طبية MeSH: Lymphoma, Non-Hodgkin/*genetics, Cytokines/metabolism ; Folic Acid/metabolism ; Humans ; Lymphoma, Non-Hodgkin/metabolism

عنوان ترانسليتريتد: Analiz deletsionnykh mutatsiĭ v gene PARK2 u bol'nykh idiopaticheskoĭ formoĭ bolezni Parkinsona.

المؤلفون: Slominskiĭ PA; Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, 123182 Russia. slomin@ras.ru, Miloserdova OV, Popova SN, Giliazova IR, Khidiiatova IV, Magzhanov RV, Khusnutdinova EK, Limborskaia SA

المصدر: Genetika [Genetika] 2003 Feb; Vol. 39 (2), pp. 223-8.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Izdatelstvo Nauka Country of Publication: Russia (Federation) NLM ID: 0047354 Publication Model: Print Cited Medium: Print ISSN: 0016-6758 (Print) Linking ISSN: 00166758 NLM ISO Abbreviation: Genetika Subsets: MEDLINE

مواضيع طبية MeSH: Sequence Deletion* , Ubiquitin-Protein Ligases*, Ligases/*genetics , Parkinson Disease/*genetics, Bashkiria ; DNA Mutational Analysis ; Exons ; Female ; Heterozygote ; Humans ; Image Interpretation, Computer-Assisted ; Male ; Middle Aged ; Parkinson Disease/etiology ; Polymerase Chain Reaction/methods