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Identification of V3 mutations that can compensate for inactivating mutations in C4 of simian immunodeficiency virus.Academic Article Why?
Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations.Academic Article Why?
Spectrum of factor XI (F11) mutations in the UK population--116 index cases and 140 mutations.Academic Article Why?
Suppression of Escherichia coli recF mutations by recA-linked srfA mutations.Academic Article Why?
Lodato, MichaelPerson Why?
Schiffer, CeliaPerson Why?
Central precocious puberty caused by mutations in the imprinted gene MKRN3.Academic Article Why?
A germline point mutation in Runx1 uncouples its role in definitive hematopoiesis from differentiation.Academic Article Why?
Chronic neutrophilic leukemia in a child with a CSF3R T618I germ line mutation.Academic Article Why?
No association between BRCA mutations and sex ratio in offspring of Pakistani BRCA mutation carriers.Academic Article Why?
Somatic mutations of epidermal growth factor receptor in colorectal carcinoma.Academic Article Why?
Distinguishable effects of presenilin-1 and APP717 mutations on amyloid plaque deposition.Academic Article Why?
Hierarchy in somatic mutations arising during genomic evolution and progression of follicular lymphoma.Academic Article Why?
Linked-read analysis identifies mutations in single-cell DNA-sequencing data.Academic Article Why?
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.Academic Article Why?
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