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 5702 of 10600

Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer.
The pharmacogenomics journal | 2014-06-01 | PMID 23999597
Yao S, Sucheston L E, Zhao H and 18 more
Genes: ABCC1, ABCB1
Molecular models and mutational analyses of plant specifier proteins suggest active site residues and reaction mechanism.
Plant molecular biology | 2014-01-01 | PMID 23999604
Brandt Wolfgang, Backenköhler Anita, Schulze Eva and 4 more
Prevention, management and extent of adverse pregnancy outcomes in women with hereditary antithrombin deficiency.
Annals of hematology | 2014-03-01 | PMID 23999648
Rogenhofer Nina, Bohlmann Michael K, Beuter-Winkler Petra and 4 more
A literature search tool for intelligent extraction of disease-associated genes.
Journal of the American Medical Informatics Association : JAMIA | 2000-01-01 | PMID 23999671
Jung Jae-Yoon, DeLuca Todd F, Nelson Tristan H and 1 more
Molecular epidemiology of Flavobacterium psychrophilum from Swiss fish farms.
Diseases of aquatic organisms | 2013-09-03 | PMID 23999704
Strepparava Nicole, Nicolas Pierre, Wahli Thomas and 2 more
CD226 rs763361 (Gly307Ser) polymorphism is associated with susceptibility to rheumatoid arthritis in Zahedan, southeast Iran.
Iranian biomedical journal | 2013-01-01 | PMID 23999715
Hashemi Mohammad, Zakeri Zahra, Eskandari-Nasab Ebrahim and 5 more
Engineering and kinetic stabilization of the therapeutic enzyme Anabeana variabilis phenylalanine ammonia lyase.
Applied biochemistry and biotechnology | 2013-12-01 | PMID 23999738
Jaliani Hossein Zarei, Farajnia Safar, Mohammadi Seyyed Abolghasem and 2 more
A phase II clinical study of mFOLFOX6 plus bevacizumab as first-line therapy for Japanese advanced/recurrent colorectal cancer patients.
Japanese journal of clinical oncology | 2013-11-01 | PMID 23999770
Nishina Tomohiro, Takano Yoshinao, Denda Tadamichi and 9 more
Genes: ERCC1, GSTP1
A possible genetic association with chronic fatigue in primary Sjögren's syndrome: a candidate gene study.
Rheumatology international | 2014-02-01 | PMID 23999819
Norheim Katrine Brække, Le Hellard Stephanie, Nordmark Gunnel and 6 more
Genes: PKN1
Association between single-nucleotide polymorphisms of OGG1 gene and pancreatic cancer risk in Chinese Han population.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2014-01-01 | PMID 23999824
Chen Hongxu, Zhou Bo, Lan Xiang and 3 more
Genes: OGG1
Inactivation of Vhl in osteochondral progenitor cells causes high bone mass phenotype and protects against age-related bone loss in adult mice.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2014-04-01 | PMID 23999831
Weng Tujun, Xie Yangli, Huang Junlan and 5 more
Genes: VHL
K-RAS mutation profile in Puerto Rican patients with colorectal cancer: trends from April 2009 to January 2011.
The International journal of biological markers | 2013-12-17 | PMID 23999847
Ruiz-Candelaria Yelitza, Miranda-Diaz Christine, Hunter-Mellado Robert F
Genes: EGFR
Role of the renin-angiotensin-aldosterone system and the glutathione S-transferase Mu, Pi and Theta gene polymorphisms in cardiotoxicity after anthracycline chemotherapy for breast carcinoma.
The International journal of biological markers | 2013-12-17 | PMID 23999848
Vivenza Daniela, Feola Mauro, Garrone Ornella and 3 more
Genes: GSTP1, ACE, AGT, GSTT1
Free-energy computations identify the mutations required to confer trans-sialidase activity into Trypanosoma rangeli sialidase.
Proteins | 2014-03-01 | PMID 23999862
Pierdominici-Sottile Gustavo, Palma Juliana, Roitberg Adrian E
A diagnostic algorithm to identify paired tumors with clonal origin.
Genes, chromosomes & cancer | 2013-11-01 | PMID 23999905
Nemes Szilárd, Danielsson Anna, Parris Toshima Z and 5 more
Haploid plants carrying a sodium azide-induced mutation (fdr1) produce fertile pollen grains due to first division restitution (FDR) in maize (Zea mays L.).
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2013-12-01 | PMID 23999907
Sugihara Naho, Higashigawa Takeyuki, Aramoto Daiki and 1 more
NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR.
Genes, chromosomes & cancer | 2013-11-01 | PMID 23999921
Akiki Susanna, Dyer Sara A, Grimwade David and 11 more
Genes: NSD1, NUP98, FLT3, NPM1
Epigenetic susceptibility factors for prostate cancer with aging.
The Prostate | 2013-12-01 | PMID 23999928
Damaschke N A, Yang B, Bhusari S and 2 more
Genes: IGF2, GSTP1
The diverse role of miR-31 in regulating cancer associated phenotypes.
Genes, chromosomes & cancer | 2013-12-01 | PMID 23999990
Laurila Eeva M, Kallioniemi Anne
Ursocholanic acid rescues mitochondrial function in common forms of familial Parkinson's disease.
Brain : a journal of neurology | 2013-10-01 | PMID 24000005
Mortiboys Heather, Aasly Jan, Bandmann Oliver
Cost-effectiveness analysis of triple therapy with protease inhibitors in treatment-naive hepatitis C patients.
PharmacoEconomics | 2013-10-01 | PMID 24000086
Blázquez-Pérez Antonio, San Miguel Ramón, Mar Javier
Relationship of Mediterranean diet and caloric intake to phenoconversion in Huntington disease.
JAMA neurology | 2013-11-01 | PMID 24000094
Marder Karen, Gu Yian, Eberly Shirley and 4 more
Hypomorphic NOTCH3 alleles do not cause CADASIL in humans.
Human mutation | 2013-11-01 | PMID 24000151
Rutten Julie W, Boon Elles M J, Liem Michael K and 9 more
Genes: NOTCH3
Tafamidis (Vyndaqel): a light for FAP patients.
ChemMedChem | 2013-10-01 | PMID 24000164
Nencetti Susanna, Rossello Armando, Orlandini Elisabetta
Genes: TTR, FAP
UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene.
Human mutation | 2013-12-01 | PMID 24000165
Wake Naomi C, Ricketts Christopher J, Morris Mark R and 10 more
Genes: CCNE1, MET, VHL
GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
Human mutation | 2013-12-01 | PMID 24000169
Yang Yi-Qing, Gharibeh Lara, Li Ruo-Gu and 12 more
Genes: GATA4, TBX5
Small insertions are more deleterious than small deletions in human genomes.
Human mutation | 2013-12-01 | PMID 24000181
Huang Shengfeng, Li Jie, Xu Anlong and 2 more
Molecular characterization of Klebsiella pneumoniae carbapenemase-producing isolates in southern Brazil.
Journal of medical microbiology | 2013-11-01 | PMID 24000225
Ribeiro Vanessa Bley, Andrade Leonardo Neves, Linhares Adriano Rostirolla and 4 more
A novel splicing mutation of KIT results in piebaldism and auburn hair color in a Chinese family.
BioMed research international | 2013-01-01 | PMID 24000325
Yang Yong-jia, Zhao Rui, He Xin-yu and 7 more
Genes: KIT
[Genotypic differences between Corynebacterium diphtheriae biovar gravis and mitis strains].
Zhurnal mikrobiologii, epidemiologii i immunobiologii | 2000-01-01 | PMID 24000590
Borisova O Iu, Volozhantsev N V, Mel'nikov V G and 3 more
[Presence of Yersinia enterocolitica in conditions of agro complex].
Zhurnal mikrobiologii, epidemiologii i immunobiologii | 2000-01-01 | PMID 24000591
Iurova M A, Pushkareva V I, Poliakov V Iu
Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis.
Clinical genetics | 2014-01-01 | PMID 24000781
Tun N M, Villani G, Ong K and 2 more
Genes: BRCA1
Phenotypic heterogeneity is a selected trait in natural yeast populations subject to environmental stress.
Environmental microbiology | 2014-06-01 | PMID 24000788
Holland Sara L, Reader Tom, Dyer Paul S and 1 more
Enzyme-dependent lysine deprotonation in EZH2 catalysis.
Biochemistry | 2013-10-01 | PMID 24000826
Kipp D Randal, Quinn Christopher M, Fortin Pascal D
Genes: SET
Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience.
Clinical genetics | 2014-09-01 | PMID 24000829
Liao C, Fu F, Li R and 4 more
Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents.
Journal of cognitive neuroscience | 2014-01-01 | PMID 24001007
Söderqvist Stina, Matsson Hans, Peyrard-Janvid Myriam and 2 more
Genes: DRD2, BDNF, COMT, DRD4, MAOA
Lens subluxation and retinal dysfunction in a girl with homozygous VSX2 mutation.
Ophthalmic genetics | 2015-03-01 | PMID 24001013
Khan Arif O, Aldahmesh Mohammed A, Noor Jawaher and 2 more
Genes: VSX2, ERG
De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients.
Ophthalmic genetics | 2015-03-01 | PMID 24001014
Zou Xuan, Yao Fengxia, Liang Xiaofang and 4 more
Genes: CRX
Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome.
Ophthalmic genetics | 2015-06-01 | PMID 24001015
Abu-Amero Khaled K, Kondkar Altaf, Hellani Ali M and 3 more
Genes: CHN1, CHRNB3, HOXA1, SALL4, TUBB3
A novel CYP1B1 mutation with congenital glaucoma and total aniridia.
Ophthalmic genetics | 2015-03-01 | PMID 24001018
Alzuhairy Sultan, Abu-Amero Khaled K, Al-Shahwan Sami and 1 more
The neurophysiologic types of nonconvulsive status epilepticus: EEG patterns of different phenotypes.
Epilepsia | 2013-09-01 | PMID 24001065
Sutter Raoul, Kaplan Peter W
Deep submersion: severe phenotype of deciduous-molar infraocclusion with biological associations.
The Angle orthodontist | 2014-03-01 | PMID 24001108
Shalish Miriam, Har-Zion Gilad, Zini Avraham and 2 more
Pharmacogenetic analysis of SNPs in genes involved in the pharmacokinetics and response to lopinavir/ritonavir therapy.
Current drug metabolism | 2013-09-01 | PMID 24001122
López Aspiroz E, Cabrera Figueroa S E, Porras Hurtado G L and 3 more
Molecular characterization and identification of members of the Anopheles subpictus complex in Sri Lanka.
Malaria journal | 2013-08-30 | PMID 24001126
Surendran Sinnathamby N, Sarma Devojit K, Jude Pavilupillai J and 6 more
Hematopoietic stem cell mobilization for gene therapy: superior mobilization by the combination of granulocyte-colony stimulating factor plus plerixafor in patients with β-thalassemia major.
Human gene therapy | 2013-10-01 | PMID 24001178
Yannaki Evangelia, Karponi Garyfalia, Zervou Fani and 8 more
Developing a rapid throughput screen for detection of nematicidal activity of plant cysteine proteinases: the role of Caenorhabditis elegans cystatins.
Parasitology | 2014-02-01 | PMID 24001183
Phiri A M, De Pomerai D, Buttle D J and 1 more
Molecular characterization and structure analysis of HPRT in a Chinese patient with Lesch-Nyhan disease.
Nucleosides, nucleotides & nucleic acids | 2013-01-01 | PMID 24001192
Jian Wei-Xia, Peng Wen-Hui, Li Hai-Ling and 3 more
Genes: HPRT1
The replication of the association of the rs9355610 within 6p27 with Graves' disease.
Autoimmunity | 2013-09-01 | PMID 24001206
Ban Yoshiyuki, Tozaki Teruaki, Taniyama Matsuo
Bioactive cytokinins are selectively secreted by Sinorhizobium meliloti nodulating and nonnodulating strains.
Molecular plant-microbe interactions : MPMI | 2013-10-01 | PMID 24001254
Kisiala Anna, Laffont Carole, Emery R J Neil and 1 more
Solving the mystery of human sleep schedules one mutation at a time.
Critical reviews in biochemistry and molecular biology | 2000-01-01 | PMID 24001255
Hallows William C, Ptáček Louis J, Fu Ying-Hui
Identification of a novel assemblage G subgenotype and a zoonotic assemblage B in rodent isolates of Giardia duodenalis in the Canary Islands, Spain.
Parasitology | 2014-02-01 | PMID 24001274
Fernández-Álvarez Ángela, Martín-Alonso Aarón, Abreu-Acosta Néstor and 4 more
First report of detection and molecular confirmation of Plasmodium ovale from severe malaria cases in central India.
Tropical medicine & international health : TM & IH | 2013-11-01 | PMID 24001284
Singh R, Jain V, Singh P P and 4 more
The interacting effects of diversity and propagule pressure on early colonization and population size.
The Journal of animal ecology | 2014-01-01 | PMID 24001312
Hedge Luke H, Leung Brian, O'Connor Wayne A and 1 more
Relationship between apolipoprotein E gene polymorphism with triglyceride level in patients with renal diseases.
Renal failure | 2013-01-01 | PMID 24001346
Dong Chun-Qiang, Luo Yi-Ge, Dong Kun and 3 more
Default network connectivity as a vulnerability marker for obsessive compulsive disorder.
Psychological medicine | 2014-05-01 | PMID 24001350
Peng Z W, Xu T, He Q H and 7 more
National mutation study among Danish patients with hereditary haemorrhagic telangiectasia.
Clinical genetics | 2014-08-01 | PMID 24001356
Tørring P M, Brusgaard K, Ousager L B and 2 more
Genes: ACVRL1, ENG, SMAD4
Classic Ehlers-Danlos syndrome: case report and brief review of literature.
Acta dermatovenerologica Croatica : ADC | 2013-01-01 | PMID 24001420
Morais Paulo, Ferreira Olga, Magina Sofia and 4 more
Genetic overlap between evoked frontocentral theta-band phase variability, reaction time variability, and attention-deficit/hyperactivity disorder symptoms in a twin study.
Biological psychiatry | 2014-02-01 | PMID 24001472
McLoughlin Gráinne, Palmer Jason A, Rijsdijk Fruhling and 1 more
Wheezing in preschool children.
Early human development | 2013-10-01 | PMID 24001476
Tenero Laura, Tezza Giovanna, Cattazzo Elena and 1 more
Defining a comprehensive verotype using electronic health records for personalized medicine.
Journal of the American Medical Informatics Association : JAMIA | 2013-12-01 | PMID 24001516
Boland Mary Regina, Hripcsak George, Shen Yufeng and 2 more
Temporal and spatial variation in Anaplasma phagocytophilum infection in Swedish moose (Alces alces).
Epidemiology and infection | 2014-06-01 | PMID 24001524
Malmsten J, Widén D Gavier, Rydevik G and 7 more
GCK-MODY diabetes as a protein misfolding disease: the mutation R275C promotes protein misfolding, self-association and cellular degradation.
Molecular and cellular endocrinology | 2014-01-25 | PMID 24001579
Negahdar Maria, Aukrust Ingvild, Molnes Janne and 9 more
Genes: GCK
Identification of sturgeon IgD bridges the evolutionary gap between elasmobranchs and teleosts.
Developmental and comparative immunology | 2014-02-01 | PMID 24001581
Zhu Lin, Yan Zhenxin, Feng Mengyang and 5 more
Gene-based polymorphisms, genomic organization of interferon-β promoter stimulator 1 (IPS-1) gene and association study with the natural resistance to grass carp reovirus in grass carp Ctenopharyngodon idella.
Developmental and comparative immunology | 2013-12-01 | PMID 24001582
Wan Quanyuan, Su Jianguo, Chen Xiaohui and 1 more
Latent profile analysis of healthy schizotypy within the extended psychosis phenotype.
Psychiatry research | 2013-12-30 | PMID 24001585
Tabak Naomi Tuchman, Weisman de Mamani Amy Gina
Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.
Human molecular genetics | 2014-01-15 | PMID 24001599
Zhang Jing, Zhang Yan, Yang Jing and 41 more
Genes: CXCR5, DDX6, PHLDB1
Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke.
Human molecular genetics | 2014-01-15 | PMID 24001601
Murray Lydia S, Lu Yinhui, Taggart Aislynn and 5 more
HNRNPA1 regulates HMGCR alternative splicing and modulates cellular cholesterol metabolism.
Human molecular genetics | 2014-01-15 | PMID 24001602
Yu Chi-Yi, Theusch Elizabeth, Lo Kathleen and 4 more
Genes: HNRNPA1, HMGCR, APOB
Successful fertilization requires the presence of at least one major O-acetylserine(thiol)lyase for cysteine synthesis in pollen of Arabidopsis.
Plant physiology | 2013-10-01 | PMID 24001608
Birke Hannah, Heeg Corinna, Wirtz Markus and 1 more
Establishment and characterization of a novel HPV-negative laryngeal squamous cell carcinoma cell line, FD-LSC-1, with missense and nonsense mutations of TP53 in the DNA-binding domain.
Cancer letters | 2014-01-01 | PMID 24001612
Wu Chun-Ping, Zhou Liang, Gong Hong-Li and 4 more
Genes: EGFR
Identification of novel OTOF compound heterozygous mutations by targeted next-generation sequencing in a Chinese patient with auditory neuropathy spectrum disorder.
International journal of pediatric otorhinolaryngology | 2013-10-01 | PMID 24001616
Zhang Lu-ping, Chai Yong-Chuan, Yang Tao and 1 more
Genes: OTOF
Biosafety assessment of titanium dioxide nanoparticles in acutely exposed nematode Caenorhabditis elegans with mutations of genes required for oxidative stress or stress response.
Chemosphere | 2013-11-01 | PMID 24001673
Rui Qi, Zhao Yunli, Wu Qiuli and 2 more
A novel strategy for plant breeding based on simulations of gene network models.
International journal of bioinformatics research and applications | 2013-01-01 | PMID 24001725
Cai X, Das S, Welch S M
Historic demography and phylogenetic relationship of Euthynnus species based on COI sequence analyses.
International journal of bioinformatics research and applications | 2013-01-01 | PMID 24001727
Kumar Girish, Kunal Swaraj Priyaranjan
The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.
Experimental cell research | 2013-11-15 | PMID 24001739
Al-Saaidi Rasha, Rasmussen Torsten B, Palmfeldt Johan and 7 more
Genes: LMNA
Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature in patients initially classified as idiopathic short stature.
The Journal of clinical endocrinology and metabolism | 2013-10-01 | PMID 24001744
Vasques Gabriela A, Amano Naoko, Docko Ana J and 6 more
Genes: NPR2
RNF43 mutations are recurrent in Chinese patients with mucinous ovarian carcinoma but absent in other subtypes of ovarian cancer.
Gene | 2013-11-15 | PMID 24001777
Zou Yang, Wang Feng, Liu Fa-Ying and 5 more
Genes: RNF43, DICER1, TRRAP
1914G variant of BCHE gene associated with enzyme activity, obesity and triglyceride levels.
Gene | 2013-12-10 | PMID 24001779
Lima Jovana Karoline, Leite Neiva, Turek Luciane Viater and 5 more
Genes: BCHE
Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.
Gene | 2013-11-15 | PMID 24001780
Martín-Morales R, García-Díaz J D, Tarugi P and 6 more
Genes: APOB, MTTP, ANGPTL3, PCSK9
Sixteen novel mutations in the arylsulfatase A gene causing metachromatic leukodystrophy.
Gene | 2013-11-10 | PMID 24001781
Luzi Paola, Rafi Mohammad A, Rao Han Zhi and 1 more
Genes: ARSA
Effect of genetic and phenotypic factors on the composition of commercial marmande type tomatoes studied through HRMAS NMR spectroscopy.
Food chemistry | 2014-01-01 | PMID 24001806
Iglesias María José, García López Jesús, Collados Luján Juan Fernando and 4 more
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci.
Hypertension (Dallas, Tex. : 1979) | 2013-11-01 | PMID 24001895
Kelly Tanika N, Takeuchi Fumihiko, Tabara Yasuharu and 54 more
Genes: FGF5, MAP4, NPR3
Functional dissection of myosin binding protein C phosphorylation.
Journal of molecular and cellular cardiology | 2013-11-01 | PMID 24001940
Gupta Manish K, Gulick James, James Jeanne and 3 more
Genes: ADA, SDS
Expression profiling of two stress-inducible genes encoding for miraculin-like proteins in citrus plants under insect infestation or salinity stress.
Journal of plant physiology | 2014-01-01 | PMID 24001970
Podda A, Simili M, Del Carratore R and 3 more
Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencing.
Genomics | 2000-01-01 | PMID 24001973
Dinwiddie Darrell L, Bracken Julia M, Bass Julie A and 9 more
Outbreak of postoperative empyema caused by Serratia marcescens in a thoracic surgery unit.
The Journal of hospital infection | 2013-11-01 | PMID 24001998
Ulu-Kilic A, Parkan O, Ersoy S and 5 more
MSI2 expression is decreased in grade II of gastric carcinoma.
Pathology, research and practice | 2013-11-01 | PMID 24002004
Emadi-Baygi Modjtaba, Nikpour Parvaneh, Mohammad-Hashem Faezeh and 2 more
Genes: MSI2, MSI1
Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.
Nature communications | 2013-01-01 | PMID 24002024
Baraban Scott C, Dinday Matthew T, Hortopan Gabriela A
A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.
Translational psychiatry | 2013-09-03 | PMID 24002087
Martin P-M, Yang X, Robin N and 9 more
Genes: WNT1, MAF
Novel organization of the arginine catabolic mobile element and staphylococcal cassette chromosome mec composite island and its horizontal transfer between distinct Staphylococcus aureus genotypes.
Antimicrobial agents and chemotherapy | 2013-11-01 | PMID 24002094
Sabat Artur J, Köck Robin, Akkerboom Viktoria and 4 more
Causal role of single nucleotide polymorphisms within the mprF gene of Staphylococcus aureus in daptomycin resistance.
Antimicrobial agents and chemotherapy | 2013-11-01 | PMID 24002096
Yang Soo-Jin, Mishra Nagendra N, Rubio Aileen and 1 more
Genes: DAP
A statistical variant calling approach from pedigree information and local haplotyping with phase informative reads.
Bioinformatics (Oxford, England) | 2013-11-15 | PMID 24002111
Kojima Kaname, Nariai Naoki, Mimori Takahiro and 4 more
M2SG: mapping human disease-related genetic variants to protein sequences and genomic loci.
Bioinformatics (Oxford, England) | 2013-11-15 | PMID 24002112
Ji Renkai, Cong Qian, Li Wenlin and 1 more
Haplotype structure and positive selection at TLR1.
European journal of human genetics : EJHG | 2014-04-01 | PMID 24002163
Heffelfinger Christopher, Pakstis Andrew J, Speed William C and 6 more
Genes: TLR1
Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon.
European journal of human genetics : EJHG | 2014-04-01 | PMID 24002164
Yasmeen Saiqa, Lund Katrine, De Paepe Anne and 6 more
Novel cardiovascular findings in association with a POMT2 mutation: three siblings with α-dystroglycanopathy.
European journal of human genetics : EJHG | 2014-04-01 | PMID 24002165
Martinez Hugo R, Craigen William J, Ummat Monika and 3 more
Genes: POMT2
Differential genotypic evolution of HIV-1 quasispecies in cerebrospinal fluid and plasma: a systematic review.
AIDS reviews | 2000-01-01 | PMID 24002199
Stam Arjen J, Nijhuis Monique, van den Bergh Walter M and 1 more
Mutational analysis of a red fluorescent protein-based calcium ion indicator.
Sensors (Basel, Switzerland) | 2013-09-02 | PMID 24002228
Carlson Haley J, Campbell Robert E
Patterns of cyto-nuclear linkage disequilibrium in Silene latifolia: genomic heterogeneity and temporal stability.
Heredity | 2014-02-01 | PMID 24002238
Fields P D, McCauley D E, McAssey E V and 1 more
Mating patterns and pollinator mobility are critical traits in forest fragmentation genetics.
Heredity | 2015-08-01 | PMID 24002239
Breed M F, Ottewell K M, Gardner M G and 3 more