共 47 条
- [31] ANALYSIS OF TARGETED KINASE DOMAIN MUTATIONS, BCR-ABL1 TRANSCRIPT TYPE AND TRI-COLOUR DUAL FUSION INTERPHASE FISH CYTOGENETICS AMONG IMATINIB-RESISTANT CHRONIC MYELOGENOUS LEUKEMIA PATIENTSINTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2018, 40 : 20 - 21Bommannan, KarthikNaseem, ShanoVarma, NeelamMalhotra, PankajBinota, JogeshwarVarma, Subhash
- [32] Differential functional phenotypes of two primary HIV-1 strains resulting from homologous point mutations in the LLP domains of the envelope gp41 intracytoplasmic domainVIROLOGY, 2007, 367 (01) : 102 - 116Newman, Jason T.Sturgeon, Timothy J.Gupta, PhalguniMontelaro, Ronald C.
- [34] Platyspondylic lethal dysplasia torrance type with a heterozygous mutation in the triple helical domain of COL2A1 in two sibs from phenotypically normal parentsAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (08) : 1953 - 1956Okamoto, ToshioNagaya, KenAsai, HirokoTsuchida, EtsushiNohara, FumikatsuHayashi, TokitsugiYamashita, AkikoNishimura, GenAzuma, Hiroshi
- [35] A Short N-Terminal Fragment in Front of the A1 Domain of Von Willebrand Factor Prevents the A1 from Binding the Platelet By Masking a Region Clustered By Type 2B VWD MutationsBLOOD, 2016, 128 (22)Deng, WeiWang, YingchunLollar, PeteLi, Renhao
- [36] Single- and multidrug resistance mutations to reverse transcriptase and protease inhibitors -: Human immunodeficiency virus type 1-infected patients from two geographical areas in SpainJOURNAL OF HUMAN VIROLOGY, 2000, 3 (03) : 150 - 156Pérez-Alvarez, LVillahermosa, MLCuevas, MTDelgado, EManjón, Nde Parga, EVMedrano, LContreras, GThomson, MMColomo, CTaboada, JANájera, R
- [37] Bone structure in two adult subjects with impaired minor spliceosome function resulting from RNU4ATAC mutations causing microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1)BONE, 2016, 92 : 145 - 149Kroigard, Anne BruunFrost, MortenLarsen, Martin JakobOusager, Lilian BommeFrederiksen, Anja Lisbeth
- [38] The 316-404 region of the SF1 ligand binding domain is critical for its transcriptional activity: evidence from two new mutations in 46, XY patients with opposite male and female phenotypeHORMONE RESEARCH, 2009, 72 : 364 - 365Philibert, PascalDamiani, DurvalHouang, MurielAudran, FrancoiseParis, FrancoiseSultan, Charles
- [39] Crystallization and preliminary X-ray crystallographic study of the wild type and two mutants of the CP1 hydrolytic domain from Aquifex aeolicus leucyl-tRNA synthetaseACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS, 2005, 61 : 899 - 901Cura, VOlieric, NGuichard, AWang, EDMoras, DEriani, GCavarelli, J
- [40] Intracellular Retention, Enhanced Clearance, and Defective FVIII Binding Are Common Features of Von Willebrand Factor D′-D3 Domain Mutations in Patients with Von Willebrand Disease Type 1 From the European Mcmdm-1VWD StudyBLOOD, 2012, 120 (21)Schneppenheim, ReinhardBudde, UlrichBatlle, JavierCastaman, GiancarloEikenboom, Jeroen C. J.Federici, Augusto B.Goudemand, JennyObser, TobiasOyen, FlorianRodeghiero, FrancescoSchneppenheim, SonjaPeake, Ian R.Goodeve, Anne C.