1.
BRAF V600E mutation and Its Association with Clinicopathological Features of Papillary Thyroid Cancer: A Meta-Analysis
by Li, Carol
The journal of clinical endocrinology and metabolism, 2012-12, Vol.97 (12), p.4559-4570
2.
Genomic Signature of an Avian Lilliput Effect across the K-Pg Extinction
by Berv, Jacob S
Systematic biology, 2018-01-01, Vol.67 (1), p.1-13
3.
Does Addition of BRAF V600E Mutation Testing Modify Sensitivity or Specificity of the Afirma Gene Expression Classifier in Cytologically Indeterminate Thyroid Nodules?
by Kloos, Richard T
The journal of clinical endocrinology and metabolism, 2013-04, Vol.98 (4), p.E761-E768
4.
Toward a major risk factor for atopic eczema: Meta-analysis of filaggrin polymorphism data
by Baurecht, Hansjörg, MSc
Journal of allergy and clinical immunology, 2007, Vol.120 (6), p.1406-1412
5.
Erg11 mutations associated with azole resistance in clinical isolates of Candida albicans
by Xiang, Ming-Jie
FEMS yeast research, 2013-06-01, Vol.13 (4), p.386-393
6.
Understanding the obstacle of incompatibility at residue 156 within HLA-B35 subtypes
by Manandhar, Trishna
Immunogenetics (New York), 2016-01-12, Vol.68 (4), p.247-260
7.
Novel Corticosteroid-Binding Globulin Variant That Lacks Steroid Binding Activity
by Perogamvros, I
The journal of clinical endocrinology and metabolism, 2010-10, Vol.95 (10), p.E142-E150
8.
A newly identified amino acid substitution T123I in the 14α-demethylase (Erg11p) of Candida albicans confers azole resistance
by Wu, YongQin
FEMS yeast research, 2017-05-01, Vol.17 (3)
9.
The Toll-like receptor 2 R753Q mutation modifies cytokine production and Toll-like receptor expression in atopic dermatitis
by Mrabet-Dahbi, Salima, PhD
Journal of allergy and clinical immunology, 2008, Vol.121 (4), p.1013-1019
10.
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
by Gerards, M
Journal of medical genetics, 2010-08, Vol.47 (8), p.507-512
11.
Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
by Irrthum, Alexandre
American journal of human genetics, 2000, Vol.67 (2), p.295-301
12.
Association of IL4R polymorphisms with Stevens-Johnson syndrome
by Ueta, Mayumi, MD, PhD
Journal of allergy and clinical immunology, 2007, Vol.120 (6), p.1457-1459
13.
Evidence for Variable Selective Pressures at MC1R
by Harding, Rosalind M
American journal of human genetics, 2000, Vol.66 (4), p.1351-1361
14.
A single amino acid substitution in PmrB is associated with polymyxin B resistance in clinical isolate of Pseudomonas aeruginosa
by Abraham, Neethu
FEMS microbiology letters, 2009-09-01, Vol.298 (2), p.249-254
15.
Does the ACE I/D polymorphism, alone or in combination with the ACTN3 R577X polymorphism, influence muscle power phenotypes in young, non-athletic adults?
by Rodríguez-Romo, Gabriel
European journal of applied physiology, 2010-08-24, Vol.110 (6), p.1099-1106
16.
The Clinical Spectrum of Multiple Endocrine Neoplasia Type 2a Caused by the Rare Intracellular RET Mutation S891A
by Schulte, Klaus-Martin
The journal of clinical endocrinology and metabolism, 2010-09, Vol.95 (9), p.E92-E97
17.
A Single Amino Acid Substitution Alters Omnipotent eRF1 of Dileptus to Euplotes-type Dualpotent eRF1: Standard Codon Usage May be Advantageous in Raptorial Ciliates
by Li, Ying
Protist, 2013-05, Vol.164 (3), p.440-449
18.
Combination of N149S and D171G mutations in Aeromonas caviae polyhydroxyalkanoate synthase and impact on polyhydroxyalkanoate biosynthesis
by Tsuge, Takeharu
FEMS microbiology letters, 2007-12-01, Vol.277 (2), p.217-222
19.
Principal Component Analysis of Binding Energies for Single-Point Mutants of hT2R16 Bound to an Agonist Correlate with Experimental Mutant Cell Response
by Chen, Derek E
Journal of computational biology, 2015-01-01, Vol.22 (1), p.37-53
20.
Oxidative stress, Helicobacter pylori, and OGG1 Ser326Cys, XPC Lys939Gln, and XPD Lys751Gln polymorphisms in a Turkish population with colorectal carcinoma
by Engin, Ayse Basak
Genetic testing and molecular biomarkers, 2010-08, Vol.14 (4), p.559-564
