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Atlas of Genetics and Cytogenetics in Oncology and Haematology最新文献

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t(1;19)(q22;p13.2) MEF2D/DAZAP1 t（1；19）（q22；p13.2）MEF2D/DAZAP1
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70681
Tl Gindina
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引用次数: 0
Cutaneous mastocytosis 皮肤肥大细胞增生症
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70659
Karen M. Chisholm
{"title":"Cutaneous mastocytosis","authors":"Karen M. Chisholm","doi":"10.4267/2042/70659","DOIUrl":"https://doi.org/10.4267/2042/70659","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44367703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
KLK6 (kallikrein-related peptidase 6) KLK6（激肽释放酶相关肽酶6）
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70658
P. Karousi, C. Kontos, A. Scorilas
{"title":"KLK6 (kallikrein-related peptidase 6)","authors":"P. Karousi, C. Kontos, A. Scorilas","doi":"10.4267/2042/70658","DOIUrl":"https://doi.org/10.4267/2042/70658","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
t(2;11)(p23;q12.3) EEF1G/ALK t / 2; 11) (p23; q12。3)EEF1G /构成的
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70660
Luigi Cristiano
{"title":"t(2;11)(p23;q12.3) EEF1G/ALK","authors":"Luigi Cristiano","doi":"10.4267/2042/70660","DOIUrl":"https://doi.org/10.4267/2042/70660","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ALDH1A1 (Aldehyde Dehydrogenase 1 family member A1) ALDH1A1(醛脱氢酶1家族成员A1)
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70676
S. Tunçer, Rümeysa Çamlica, Idris Yilmaz
{"title":"ALDH1A1 (Aldehyde Dehydrogenase 1 family member A1)","authors":"S. Tunçer, Rümeysa Çamlica, Idris Yilmaz","doi":"10.4267/2042/70676","DOIUrl":"https://doi.org/10.4267/2042/70676","url":null,"abstract":"Aldehyde dehydrogenase 1A1 (ALDH1A1) is a member of the ALDH gene superfamily. Aldehyde dehydrogenases (ALDHs) are responsible for the metabolism of aldehydes (exogenous and endogenous) through NAD(P)-dependent oxidation to their corresponding carboxylic acids or CoA esters. Different biological functions have been attributed to the different ALDH family members. The cytosolic enzyme ALDH1A1 is involved in the catalysis of retinol (vitamin A) metabolite retinaldehyde to retinoic acid (RA). RA acts as a ligand for the nuclear receptors retinoic receptor (RAR) and the retinoid X receptor (RXR) and therefore regulates the transcriptional activity of genes involved in multiple important processes including proliferation, differentiation, and apoptosis.","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Retinoblastoma (hereditary predisposition) 视网膜母细胞瘤(遗传易感性)
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70662
F. Ariani, A. Pinto, A. Renieri
{"title":"Retinoblastoma (hereditary predisposition)","authors":"F. Ariani, A. Pinto, A. Renieri","doi":"10.4267/2042/70662","DOIUrl":"https://doi.org/10.4267/2042/70662","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
EEF1G (Eukaryotic translation elongation factor 1 gamma) 真核翻译延伸因子1 γ
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70656
L. Cristiano
{"title":"EEF1G (Eukaryotic translation elongation factor 1 gamma)","authors":"L. Cristiano","doi":"10.4267/2042/70656","DOIUrl":"https://doi.org/10.4267/2042/70656","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
EEF1D (eukaryotic translation elongation factor 1 delta) 真核翻译延伸因子1 δ
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70678
L. Cristiano
{"title":"EEF1D (eukaryotic translation elongation factor 1 delta)","authors":"L. Cristiano","doi":"10.4267/2042/70678","DOIUrl":"https://doi.org/10.4267/2042/70678","url":null,"abstract":"Eukaryotic translation elongation factor 1 delta, alias EEF1D, is a protein-coding gene that plays a role in the elongation step of translation and considering its importance it is found frequently overexpressed in human cancer cells. This review collects the data on DNA/RNA, on the protein encoded and on the diseases where EEF1D is involved.","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
t(1;19)(q22;p13.2) MEF2D/HNRNPUL1 t（1；19）（q22；p13.2）MEF2D/HNRNPUL1
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2020-01-01 DOI: 10.4267/2042/70682
Tl Gindina
{"title":"t(1;19)(q22;p13.2) MEF2D/HNRNPUL1","authors":"Tl Gindina","doi":"10.4267/2042/70682","DOIUrl":"https://doi.org/10.4267/2042/70682","url":null,"abstract":"","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70516543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
i(3)(q10) in non-Hodgkin's lymphoma (NHL) i(3)(q10)在非霍奇金淋巴瘤(NHL)中的表达
Atlas of Genetics and Cytogenetics in Oncology and Haematology Pub Date : 2019-12-01 DOI: 10.4267/2042/70608
A. Zámečníkova
{"title":"i(3)(q10) in non-Hodgkin's lymphoma (NHL)","authors":"A. Zámečníkova","doi":"10.4267/2042/70608","DOIUrl":"https://doi.org/10.4267/2042/70608","url":null,"abstract":"Partial or complete chromosome 3 gains resulting from the presence of trisomy 3, unbalanced translocation or isochromosome formation has been observed in different types of non-Hodgkin's lymphomas (NHL). Among them, the isochromosome of the long arm of chromosome 3 is a relatively rare chromosome aberration, associated mainly with B-cell NHL. However, its occurrence is not restricted to lymphomas, as the detection of +i(3)(q10) is considered a specific marker of polyclonal B-cell lymphocytosis with binucleated lymphocytes (PPBL) associated with an increase frequency of chromosome 3 instability as well as it may also be found in myeloid malignancies.","PeriodicalId":52212,"journal":{"name":"Atlas of Genetics and Cytogenetics in Oncology and Haematology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46418611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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