mutation
164 results
1 - 100
mutation- inactivating mutation
- conservative mutation
- induced mutation
- JAK2 mutation
- loss-of-function mutation
- missense mutation
- natural mutation
- nonconservative mutation
- nonsense mutation
- null mutation
- passenger mutation
- driver mutation
- point mutation
- regulatory mutation
- silent mutation
- somatic mutation
- targeted mutation
- transparent mutation
- engineered mutation
- escape mutation
- factor V Leiden mutation
- founder mutation
- frameshift mutation
- gain-of-function mutation
- germline mutation
- JAK2 mutation
- mutation frequency
- PIK3CA mutation
- mutagenesis
vemurafenib- dabrafenib
- gene
- ivosidenib
- encorafenib
- escape
- mutational escape
- trametinib
- channelopathy
- binimetinib
- elexacaftor/tezacaftor/ivacaftor
- hypermutability
- tezacaftor/ivacaftor
- revertant
- enasidenib
- dissociation
- sport
- mitochondriopathy
- idiovariation
- mutein
- cobimetinib
- gilteritinib
- deafness
- lumacaftor/ivacaftor
Glomerulonephritis, Acute- eteplirsen
- golodirsen
- microsatellite
- enzymopathy
- capmatinib
- delta F-508
- transmutation
- ivacaftor
- Bartlett-Biedel syndrome
- diagnostic
- phenocopy
- factor
- asciminib
- subtype
- Denys-Drash syndrome
- mosaic
- midostaurin
- transversion
- dominant optic atrophy and deafness
- genotype
- panitumumab
- osimertinib
- viral breakthrough
- avapritinib
- larotrectinib
- Ghent nosology
- achondroplasia
- Guillain-Barré Syndrome
- tumor necrosis factor receptor-associated periodic syndrome
- Hemophilia
- Sickle Cell Disease
- rucaparib
- juvenile hemochromatosis
- entrectinib
- maternally inherited diabetes and deafness
- Arterial Occlusive Disease
- Goiter
- Duchenne, Guillaume B. A.
- myelofibrosis