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日期:2024-07-26
1. Leukemia. 1996 Dec;10(12):1911-8. Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Nakao M, Yokota S, Iwai T, Kaneko H, Horiike S, Kashima K, Sonoda Y, Fujimoto T, Misawa S. We analyzed mRNA expression of the flt3 gene in ....
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日期:2024-07-23
Complete information for CDK1 gene (protein-coding), cyclin-dependent kinase 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium ... Function for CDK1 gene (According to 1 UniProtKB, Gena...
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日期:2024-07-22
Human papillomaviruses (HPV) are the etiological agents responsible for a number of pathologies affecting the stratified epithelia of the skin and anogenital and oropharyngeal sites [1-3]. Specific HPV types (“low risk” HPVs) cause benign warts, but other...
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日期:2024-07-25
SignaGen Laboratories, A Gene Delivery Company... : - In Vitro DNA Transfection Reagents In Vivo Transfection Reagents Pre-optimized Transfection Reagents In Vitro siRNA Transfection Reagents Transfection Accessories Pre-made Adenovirus shRNA/miRNA ......
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日期:2024-07-22
T10 (Alias) 4p15.32 CD38 T4-A (Alias) 18q21.33 SERPINB3 TAAD2 (Alias) 3p24.1 TGFBR2 TAC1 7q21.3 TAC1 (tachykinin, precursor 1) TAC2 (Alias) 7q21.3 TAC1 TACC1 8p11.22 TACC1 (transforming, acidic coiled-coil containing protein 1) TACC2 10q26.13...
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日期:2024-07-20
A biweekly scientific journal publishing high-quality research in molecular biology and genetics, cancer biology, biochemistry, and related fields ... Current status of gene annotation: impact of genetic variability The human reference genome is a haploid...
European Journal of Human Genetics - Novel FGFR3 mutations creating cysteine residues in the extrace
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日期:2024-07-23
Top of page Abstract Achondroplasia (ACH) and hypochondroplasia (HCH) are two autosomal-dominant skeletal disorders caused by recurrent missense FGFR3 mutations in the transmembrane (TM) and tyrosine kinase 1 (TK1) domains of the receptor. Although 98 ......
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日期:2024-07-24
The European Journal of Human Genetics is the official Journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports, News and Commentary articles and reviews in the rapidly expanding field of human ge...