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, family with sequence similarity 49 member A
National Institutes of Health
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Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of nonsyndromic oral clefts in the Brazilian population.
Camilla de Marchi Sanches Azevedo
A. L. Rangel
Corpus ID: 203609236
OBJECTIVE To investigate the association of single-nucleotide polymorphisms (SNP) in grainyhead-like-3 (GRHL3) and to verify its…
Identification of novel lncRNAs regulated by the TAL1 complex in T-cell acute lymphoblastic leukemia
P. C. T. Ngoc
Corpus ID: 4830549
TAL1/SCL is one of the most prevalent oncogenes in T-cell acute lymphoblastic leukemia (T-ALL). TAL1 and its regulatory partners…
Genetic variants of MGMT, RHPN2, and FAM49A contributed to susceptibility of nonsyndromic orofacial clefts in a Chinese population
Journal of oral pathology & medicine : official…
Corpus ID: 49428200
BACKGROUND The role of underlying genetic factors in the pathogenesis of nonsyndromic orofacial clefts (NSOC) remains poorly…
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Human molecular genetics
Corpus ID: 27662362
Orofacial clefts (OFCs), which include non-syndromic cleft lip with or without cleft palate (CL/P), are among the most common…
Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.
Corpus ID: 13308442
Double minutes (dmin) and homogeneously staining regions (hsr) are the cytogenetic hallmarks of genomic amplification in cancer…
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