Sneddon's syndrome: a comprehensive review of the literature.
Orphanet journal of rare diseases | 2014-12-31 | PMID 25551694
Wu Shengjun, Xu Ziqi, Liang Hui
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 6289 of 10600
The association of MDM2 c.346G>A genetic variant with the risk of osteosarcoma in Chinese.
Genetic testing and molecular biomarkers | 2015-02-01 | PMID 25551700
Hu Zhaohui, Li Ningning, Xie Xiangtao and 1 more
Genes: MDM2
Suppression of allelic recombination and aneuploidy by cohesin is independent of Chk1 in Saccharomyces cerevisiae.
PloS one | 2014-01-01 | PMID 25551702
Covo Shay, Chiou Eric, Gordenin Dmitry A and 1 more
Mice lacking the SLAM family member CD84 display unaltered platelet function in hemostasis and thrombosis.
PloS one | 2014-01-01 | PMID 25551754
Hofmann Sebastian, Braun Attila, Pozgaj Rastislav and 3 more
Co-circulation of dengue virus type 3 genotypes in Vientiane capital, Lao PDR.
PloS one | 2014-01-01 | PMID 25551768
Lao Malayvanh, Caro Valérie, Thiberge Jean-Michel and 12 more
Cell competition: winning out by losing notch.
Cell cycle (Georgetown, Tex.) | 2015-01-01 | PMID 25551772
Alcolea Maria P, Jones Philip H
Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia.
BMC infectious diseases | 2014-12-31 | PMID 25551790
Al-Anazi Mashael R, Matou-Nasri Sabine, Abdo Ayman A and 7 more
Genes: DEPDC5
Heterogeneous induction of microglia M2a phenotype by central administration of interleukin-4.
Journal of neuroinflammation | 2014-12-31 | PMID 25551794
Pepe Giovanna, Calderazzi Giorgia, De Maglie Marcella and 2 more
Circulating Apo 2L levels decreased in genotype II hepatitis C with pegylated interferon-2 alpha treatment.
Le infezioni in medicina | 2014-12-01 | PMID 25551843
Yalcin Arzu Didem, Celik Betul, Kose Sukran and 3 more
Focal epithelial hyperplasia in a Turkish family.
Le infezioni in medicina | 2014-12-01 | PMID 25551850
Gökahmetoğlu Selma, Ferahbaş Ayten, Canöz Özlem
Is there a genetic predisposition for Turkish patients with sarcoidosis in the 329-bp region containing the BTNL2 rs2076530 polymorphism?
Turkish journal of medical sciences | 2014-01-01 | PMID 25551927
Ozdemir Muhsin, Saydam Faruk, Kurt Emel and 5 more
Genes: BTNL2
Genotype distribution of hepatitis C virus in Khorasan Razavi Province, Iran.
Turkish journal of medical sciences | 2014-01-01 | PMID 25551938
Afshari Reza, Nomani Hosein, Zaniani Fatemeh Riyahi and 6 more
Hepatitis C virus genotypes in Adana and Antakya regions of Turkey.
Turkish journal of medical sciences | 2014-01-01 | PMID 25551939
Oztürk Agah Bahadir, Doğan Umit Bilge, Oztürk Nevin Akçaer and 4 more
[Microviscosity of erythrocyte membranes in breast cancer patients: connection with the receptor phenotype of the tumor].
Voprosy onkologii | 2014-01-01 | PMID 25552073
Tsyrlina E V, Kriukova O G, Poroshina T E and 5 more
Discovering missing heritability and early risk prediction for type 2 diabetes: a new perspective for genome-wide association study analysis with the Nurses' Health Study and the Health Professionals' Follow-Up Study.
Turkish journal of medical sciences | 2014-01-01 | PMID 25552146
Gül Hüsamettin, Aydin Son Yeşim, Açikel Cengizhan
Common genetic variant on 14q13.3 contributes to thyroid cancer susceptibility: evidence based on 12 studies.
Molecular genetics and genomics : MGG | 2015-06-01 | PMID 25552255
Zheng JiaoJiao, Li Chen, Wang Cong and 1 more
The evolution of selfing is accompanied by reduced efficacy of selection and purging of deleterious mutations.
Genetics | 2015-03-01 | PMID 25552275
Arunkumar Ramesh, Ness Rob W, Wright Stephen I and 1 more
A HIF-independent mediator of transcriptional responses to oxygen deprivation in Caenorhabditis elegans.
Genetics | 2015-03-01 | PMID 25552276
Padmanabha Divya, Padilla Pamela A, You Young-Jai and 1 more
New serotypes of porcine teschovirus identified in Shanghai, China.
Archives of virology | 2015-03-01 | PMID 25552321
Sun Huan, Gao Han, Chen Molin and 6 more
Influence of growth hormone receptor (GHR) exon 3 and -202A/C IGFBP-3 genetic polymorphisms on clinical and biochemical features and therapeutic outcome of patients with acromegaly.
Pituitary | 2015-10-01 | PMID 25552351
Jallad Raquel S, Trarbach Ericka B, Duarte Felipe H and 2 more
Genes: GHR, IGFBP3, IGF1
Isolation and characterization of influenza C viruses in the Philippines and Japan.
Journal of clinical microbiology | 2015-03-01 | PMID 25552361
Odagiri Takashi, Matsuzaki Yoko, Okamoto Michiko and 7 more
In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.
Mammalian genome : official journal of the International Mammalian Genome Society | 2015-02-01 | PMID 25552398
Hadsell Darryl L, Hadsell Louise A, Olea Walter and 6 more
Phase I/II study of gefitinib (Iressa(®)) and vorinostat (IVORI) in previously treated patients with advanced non-small cell lung cancer.
Cancer chemotherapy and pharmacology | 2015-03-01 | PMID 25552401
Han Ji-Youn, Lee Soo Hyun, Lee Geon Kook and 5 more
Genes: EGFR
DNA polymerase β deficiency leads to neurodegeneration and exacerbates Alzheimer disease phenotypes.
Nucleic acids research | 2015-01-01 | PMID 25552414
Sykora Peter, Misiak Magdalena, Wang Yue and 17 more
A Novel Arabidopsis microRNA promotes IAA biosynthesis via the indole-3-acetaldoxime pathway by suppressing superroot1.
Plant & cell physiology | 2015-04-01 | PMID 25552472
Kong Wenwen, Li Yong, Zhang Mengmeng and 2 more
The human IL-23 receptor rs11209026 A allele promotes the expression of a soluble IL-23R-encoding mRNA species.
Journal of immunology (Baltimore, Md. : 1950) | 2015-02-01 | PMID 25552541
Yu Raymond Y, Brazaitis Jonathan, Gallagher Grant
Genes: STAT3
Homeodomain-interacting protein kinase 2, a novel autoimmune regulator interaction partner, modulates promiscuous gene expression in medullary thymic epithelial cells.
Journal of immunology (Baltimore, Md. : 1950) | 2015-02-01 | PMID 25552543
Rattay Kristin, Claude Janine, Rezavandy Esmail and 4 more
Genes: AIRE, HIPK2, TEC
Giant ankyrin-G: a critical innovation in vertebrate evolution of fast and integrated neuronal signaling.
Proceedings of the National Academy of Sciences of the United States of America | 2015-01-27 | PMID 25552556
Jenkins Paul M, Kim Namsoo, Jones Steven L and 4 more
Genes: ANK2, ANK3
Protein design algorithms predict viable resistance to an experimental antifolate.
Proceedings of the National Academy of Sciences of the United States of America | 2015-01-20 | PMID 25552560
Reeve Stephanie M, Gainza Pablo, Frey Kathleen M and 3 more
Genes: DHFR
Interaction between hydrogen sulfide-induced sulfhydration and tyrosine nitration in the KATP channel complex.
American journal of physiology. Gastrointestinal and liver physiology | 2015-03-15 | PMID 25552582
Kang Minho, Hashimoto Atsushi, Gade Aravind and 1 more
Genome-wide association study for endothelial growth factors.
Circulation. Cardiovascular genetics | 2015-04-01 | PMID 25552591
Lieb Wolfgang, Chen Ming-Huei, Larson Martin G and 13 more
Genes: MCPH1
Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families.
Circulation. Cardiovascular genetics | 2015-02-01 | PMID 25552592
Shetty Priya B, Tang Hua, Feng Tao and 11 more
Adiponectin as a link between type 2 diabetes and vascular NADPH oxidase activity in the human arterial wall: the regulatory role of perivascular adipose tissue.
Diabetes | 2015-06-01 | PMID 25552596
Antonopoulos Alexios S, Margaritis Marios, Coutinho Patricia and 17 more
Genes: ADIPOQ
Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
Human molecular genetics | 2015-04-15 | PMID 25552646
Dong Chengliang, Wei Peng, Jian Xueqiu and 4 more
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly.
Human molecular genetics | 2015-04-15 | PMID 25552650
Hardies Katia, May Patrick, Djémié Tania and 9 more
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study.
Human molecular genetics | 2015-04-15 | PMID 25552651
Weng Lu-Chen, Cushman Mary, Pankow James S and 4 more
Genes: HRG, KNG1, VWF, ABO
Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid.
Human molecular genetics | 2015-04-15 | PMID 25552652
Riemersma Moniek, Sandrock Julia, Boltje Thomas J and 6 more
Genes: HAP1
Genetic knockdown of estrogen receptor-alpha in the subfornical organ augments ANG II-induced hypertension in female mice.
American journal of physiology. Regulatory, integrative and comparative physiology | 2015-03-15 | PMID 25552661
Xue Baojian, Zhang Zhongming, Beltz Terry G and 3 more
Genes: ANG
Deciphering the molecular landscape in chronic lymphocytic leukemia: time frame of disease evolution.
Haematologica | 2015-01-01 | PMID 25552678
Sutton Lesley-Ann, Rosenquist Richard
Role of the clathrin adaptor PICALM in normal hematopoiesis and polycythemia vera pathophysiology.
Haematologica | 2015-04-01 | PMID 25552701
Ishikawa Yuichi, Maeda Manami, Pasham Mithun and 12 more
Genes: PICALM
Mutations conferring a noncytotoxic phenotype on chikungunya virus replicons compromise enzymatic properties of nonstructural protein 2.
Journal of virology | 2015-03-01 | PMID 25552719
Utt Age, Das Pratyush Kumar, Varjak Margus and 3 more
Quantitative detection of circulating nucleophosmin mutations DNA in the plasma of patients with acute myeloid leukemia.
International journal of medical sciences | 2015-01-01 | PMID 25552914
Quan Jing, Gao Yu-jie, Yang Zai-lin and 5 more
Molecular variation and horizontal gene transfer of the homocysteine methyltransferase gene mmuM and its distribution in clinical pathogens.
International journal of biological sciences | 2015-01-01 | PMID 25552925
Ying Jianchao, Wang Huifeng, Bao Bokan and 16 more
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection.
Current protocols in bioinformatics | 2013-12-01 | PMID 25553206
Koboldt Daniel C, Larson David E, Wilson Richard K
Mitochondrial DNA aberrations and pathophysiological implications in hematopoietic diseases, chronic inflammatory diseases, and cancers.
Annals of laboratory medicine | 2015-01-01 | PMID 25553274
Kim Hye-Ran, Won Stephanie Jane, Fabian Claire and 3 more
Calreticulin exon 9 mutations in myeloproliferative neoplasms.
Annals of laboratory medicine | 2015-01-01 | PMID 25553276
Ha Jung-Sook, Kim Yu-Kyung
Genes: CALR, JAK2, MPL
Detection of the efflux-mediated erythromycin resistance transposon in Streptococcus pneumoniae.
Annals of laboratory medicine | 2015-01-01 | PMID 25553281
Azadegan Azadeh, Ahmadi Ali, Lari Abdolaziz Rastegar and 1 more
The impact of HLA and KIR ligand mismatching on unrelated allogeneic hematopoietic stem cell transplantation in Korean adult patients.
Annals of laboratory medicine | 2015-01-01 | PMID 25553290
Park Hyewon, Rho Eun Youn, In Ji Won and 6 more
Alteration of the SETBP1 gene and splicing pathway genes SF3B1, U2AF1, and SRSF2 in childhood acute myeloid leukemia.
Annals of laboratory medicine | 2015-01-01 | PMID 25553291
Choi Hyun-Woo, Kim Hye-Ran, Baek Hee-Jo and 6 more
Genes: SETBP1, SRSF2, SET
Performance of LIFECODES HLA-DQB1 typing kit using Luminex platform in Koreans.
Annals of laboratory medicine | 2015-01-01 | PMID 25553292
Roh Eun Youn, In Ji Won, Shin Sue and 3 more
Clinical relevance of high-resolution single nucleotide polymorphism array in patients with relapsed acute lymphoblastic leukemia with normal karyotype: a report of three cases.
Annals of laboratory medicine | 2015-01-01 | PMID 25553294
Park Sang Hyuk, Lee Seung-Hee, Kim Shine Young and 6 more
ABO*Ael03/O genotype with ABO discrepancy: the first case in Korea.
Annals of laboratory medicine | 2015-01-01 | PMID 25553295
Jung Bo Kyeung, Choi Gye-Ryung, Chang Jung Hee and 5 more
Genes: ABO
Non-homologous end joining repair mechanism-mediated deletion of CHD7 gene in a patient with typical CHARGE syndrome.
Annals of laboratory medicine | 2015-01-01 | PMID 25553296
Lee Seung Jun, Chae Jong Hee, Lee Jung Ae and 5 more
Genes: CHD7
The relationship of CASP 8 polymorphism and cancer susceptibility: a meta-analysis.
Cellular and molecular biology (Noisy-le-Grand, France) | 2014-12-30 | PMID 25553350
Ji G H, Li M, Cui Y and 1 more
Genes: CASP8
The role of trace elements, thiamin (e) and transketolase in autism and autistic spectrum disorder.
Frontiers in bioscience (Elite edition) | 2015-01-01 | PMID 25553376
Obrenovich Mark E, Shola Dorjee, Schroedel Kathleen and 2 more
Selective chromatid segregation mechanism for Bruchus wings piebald color.
Frontiers in bioscience (Elite edition) | 2015-01-01 | PMID 25553380
Klar Amar J S
Tumour-associated macrophage polarisation and re-education with immunotherapy.
Frontiers in bioscience (Elite edition) | 2015-01-01 | PMID 25553381
Josephs Debra H, Bax Heather J, Karagiannis Sophia N
Loss of Nfkb1 leads to early onset aging.
Aging | 2014-11-01 | PMID 25553648
Bernal Giovanna M, Wahlstrom Joshua S, Crawley Clayton D and 6 more
Genes: GFAP
A phase 2 study of bevacizumab in combination with carboplatin and paclitaxel in patients with non-squamous non-small-cell lung cancer harboring mutations of epidermal growth factor receptor (EGFR) after failing first-line EGFR-tyrosine kinase inhibitors (HANSHIN Oncology Group 0109).
Lung cancer (Amsterdam, Netherlands) | 2015-02-01 | PMID 25553650
Hattori Yoshihiro, Satouchi Miyako, Shimada Temiko and 13 more
Genes: EGFR
Review: phage therapy: a modern tool to control bacterial infections.
Pakistan journal of pharmaceutical sciences | 2015-01-01 | PMID 25553704
Qadir Muhammad Imran
Association of the insulin-like growth factor binding protein 3 (IGFBP-3) polymorphism with longevity in Chinese nonagenarians and centenarians.
Aging | 2014-11-01 | PMID 25553725
He Yong-Han, Lu Xiang, Yang Li-Qin and 2 more
Genes: ATM, FOXO3
Distribution of alpha-thalassemia mutations in Iranian population.
Hematology (Amsterdam, Netherlands) | 2015-07-01 | PMID 25553732
Dehbozorgian Javad, Moghadam Mohamad, Daryanoush Saeed and 5 more
Farnesoid x receptor in human metabolism and disease: the interplay between gene polymorphisms, clinical phenotypes and disease susceptibility.
Expert opinion on drug metabolism & toxicology | 2015-04-01 | PMID 25553772
Koutsounas Ioannis, Theocharis Stamatios, Delladetsima Ioanna and 2 more
IPED2X: a robust pedigree reconstruction algorithm for complicated pedigrees.
Journal of bioinformatics and computational biology | 2014-12-01 | PMID 25553812
He Dan, Eskin Eleazar
Novel WISP3 mutations causing spondyloepiphyseal dysplasia tarda with progressive arthropathy in two unrelated Chinese families.
Joint bone spine | 2015-03-01 | PMID 25553839
Liu Limin, Li Nan, Zhao Zhen and 2 more
Structure and interactions of the CS domain of human H/ACA RNP assembly protein Shq1.
Journal of molecular biology | 2015-02-27 | PMID 25553844
Singh Mahavir, Wang Zhonghua, Cascio Duilio and 1 more
Evaluation of the MeltPro TB/STR assay for rapid detection of streptomycin resistance in Mycobacterium tuberculosis.
Tuberculosis (Edinburgh, Scotland) | 2015-03-01 | PMID 25553930
Zhang Ting, Hu Siyu, Li Guoli and 7 more
Epigenetic mechanisms in Parkinson's disease.
Journal of the neurological sciences | 2015-02-15 | PMID 25553963
Feng Ya, Jankovic Joseph, Wu Yun-Cheng
α-Galactosidase A knockout mice: progressive organ pathology resembles the type 2 later-onset phenotype of Fabry disease.
The American journal of pathology | 2015-03-01 | PMID 25553976
Bangari Dinesh S, Ashe Karen M, Desnick Robert J and 8 more
Genetic diversity in Trypanosoma theileri from Sri Lankan cattle and water buffaloes.
Veterinary parasitology | 2015-01-30 | PMID 25554063
Yokoyama Naoaki, Sivakumar Thillaiampalam, Fukushi Shintaro and 6 more
Familial renal glycosuria and modifications of glucose renal excretion.
Diabetes & metabolism | 2014-12-01 | PMID 25554066
Prié D
The usefulness of genotyping cytochrome P450 enzymes in the treatment of depression.
Expert opinion on drug metabolism & toxicology | 2015-03-01 | PMID 25554071
Dubovsky Steven L
Targeted activation of silent natural product biosynthesis pathways by reporter-guided mutant selection.
Metabolic engineering | 2015-03-01 | PMID 25554073
Guo Fang, Xiang Sihai, Li Liyuan and 6 more
Role of cytochrome P450 genes in breast cancer etiology and treatment: effects on estrogen biosynthesis, metabolism, and response to endocrine therapy.
Cancer causes & control : CCC | 2015-03-01 | PMID 25554091
Blackburn Heather L, Ellsworth Darrell L, Shriver Craig D and 1 more
The reduction of gene expression variability from single cells to populations follows simple statistical laws.
Genomics | 2015-03-01 | PMID 25554103
Piras Vincent, Selvarajoo Kumar
Epigenetics in pediatrics.
Pediatrics in review | 2015-01-01 | PMID 25554107
Puumala Susan E, Hoyme H Eugene
Cardiac channelopathies in pediatric patients - 7-years single center experience.
Journal of electrocardiology | 2000-01-01 | PMID 25554238
Illikova V, Hlivak P, Hatala R
Multiple drug-susceptibility screening in Mycobacterium bovis: new nucleotide polymorphisms in the embB gene among ethambutol susceptible strains.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases | 2015-04-01 | PMID 25554388
Marianelli Cinzia, Armas Federica, Boniotti Maria Beatrice and 3 more
A molecular pathway analysis informs the genetic background at risk for schizophrenia.
Progress in neuro-psychopharmacology & biological psychiatry | 2015-06-03 | PMID 25554435
Crisafulli Concetta, Drago Antonio, Calabrò Marco and 2 more
A haplotype of the norepinephrine transporter gene (SLC6A2) is associated with visual memory in attention-deficit/hyperactivity disorder.
Progress in neuro-psychopharmacology & biological psychiatry | 2015-04-03 | PMID 25554436
Shang Chi-Yung, Chiang Huey-Ling, Gau Susan Shur-Fen
Genes: SRM
Triple positive breast cancer: a distinct subtype?
Cancer treatment reviews | 2015-02-01 | PMID 25554445
Vici Patrizia, Pizzuti Laura, Natoli Clara and 17 more
Link between the SNCA gene and parkinsonism.
Neurobiology of aging | 2015-03-01 | PMID 25554495
Xu Wei, Tan Lan, Yu Jin-Tai
Genes: SNCA
Relationship Among Gefitinib Exposure, Polymorphisms of Its Metabolizing Enzymes and Transporters, and Side Effects in Japanese Patients With Non-Small-Cell Lung Cancer.
Clinical lung cancer | 2015-07-01 | PMID 25554506
Kobayashi Hiroyuki, Sato Kazuhiro, Niioka Takenori and 3 more
Genes: ABCB1, ABCG2
High-throughput sequencing using the Ion Torrent personal genome machine for clinical evaluation of somatic hypermutation status in chronic lymphocytic leukemia.
The Journal of molecular diagnostics : JMD | 2015-03-01 | PMID 25554587
McClure Rebecca, Mai Ming, McClure Scott
Two novel methods for rapid detection and quantification of DNMT3A R882 mutations in acute myeloid leukemia.
The Journal of molecular diagnostics : JMD | 2015-03-01 | PMID 25554589
Mancini Melissa, Hasan Syed Khizer, Ottone Tiziana and 6 more
Study of the putative fusion regions of the preS domain of hepatitis B virus.
Biochimica et biophysica acta | 2015-04-01 | PMID 25554595
Delgado Carmen L, Núñez Elena, Yélamos Belén and 3 more
Uncommon constellation of multiglandular deficiency with 2 mutations in AIRE gene in an 18-year-old girl - 12 years of observation.
Endokrynologia Polska | 2014-01-01 | PMID 25554620
Barg Ewa, Skarżynska Małgorzata, Pollak Agnieszka and 5 more
Genes: AIRE
[Allgrove syndrome].
Annales de dermatologie et de venereologie | 2015-02-01 | PMID 25554662
Alakeel A, Raynaud C, Rossi M and 3 more
Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.
Cancer genetics | 2000-01-01 | PMID 25554686
Sherman Scott K, Maxwell Jessica E, Qian Qining and 5 more
Genes: PTEN, SMAD7, SMAD4
Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions.
Science (New York, N.Y.) | 2015-01-02 | PMID 25554788
Tomasetti Cristian, Vogelstein Bert
Hypertriglyceridemia in the genomic era: a new paradigm.
Endocrine reviews | 2015-02-01 | PMID 25554923
Lewis Gary F, Xiao Changting, Hegele Robert A
Genotypic and clinical differences of seropositive Helicobacter pylori children and adults in the Polish population.
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society | 2014-12-01 | PMID 25554984
Iwanczak B, Laszewicz W, Iwanczak F and 5 more
[Molecular detection of Saint Louis encephalitis virus in mosquitoes in Buenos Aires].
Medicina | 2014-01-01 | PMID 25555001
Beltrán Fernando J, Bechara Yamila I, Guido Guillermo G and 3 more
Phenotypic regulation of the sphingosine 1-phosphate receptor miles apart by G protein-coupled receptor kinase 2.
Biochemistry | 2015-01-27 | PMID 25555130
Burczyk Martina, Burkhalter Martin D, Blätte Tamara and 4 more
Genes: GRK2
Comparison of similar Arctic and Antarctic morphotypes of heterotrophic protists regarding their genotypes and ecotypes.
Protist | 2015-02-01 | PMID 25555150
Nitsche Frank, Arndt Hartmut
Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome.
Blood cancer journal | 2015-01-02 | PMID 25555161
Patnaik M M, Wassie E A, Padron E and 10 more
Genes: ASXL1, SRSF2
TLR4 genotype and environmental LPS mediate RSV bronchiolitis through Th2 polarization.
The Journal of clinical investigation | 2015-02-01 | PMID 25555213
Caballero Mauricio T, Serra M Elina, Acosta Patricio L and 40 more
Genes: TLR4, GATA3
ACE insertion/deletion polymorphism is associated with periodontal disease in Korean population.
Archives of oral biology | 2015-03-01 | PMID 25555251
Kang Sang Wook, Han Seung Yeop, Lim Sung Bin and 2 more
Genes: ACE
Improving identification of familial hypercholesterolaemia in primary care: derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT).
Atherosclerosis | 2015-02-01 | PMID 25555265
Weng Stephen F, Kai Joe, Andrew Neil H and 2 more
Different clinical effects upon separate inhibition of coexisting EGFR and PI3KCA mutations in a lung adenocarcinoma patient.
Lung cancer (Amsterdam, Netherlands) | 2015-02-01 | PMID 25555368
Tiseo Marcello, Bersanelli Melissa, Perrone Federica and 6 more
Genes: EGFR