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.

Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.

Publications

Page 7580 of 10600

[Rare thalassemia mutations among southern Chinese population].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188602
Lin Fen, Yang Liye, Lin Min and 5 more
Genes: HBB
[Genetic mutation and clinical features of osteogenesis imperfecta type V].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188603
Guan Shizhen, Bai Xue, Wang Yi and 6 more
Genes: IFITM5
[Analysis of 12 patients with novel mutations of Dystrophin gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188604
Xu Xiaoxin, Liu Yang, Pan Yuchun and 3 more
[Analysis of prognosis of acute myeloid leukemia patients based on genetic mutations].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188605
Shi Jinning, Zhu Yu, Hong Ming and 10 more
Genes: DNMT3A, FLT3, KIT, NPM1
[NOTCH3 gene mutations in two Chinese families featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188607
Sun Qiying, Li Wenwen, Zhou Yafang and 6 more
Genes: NOTCH3
[CADASIL with clinical manifestations of baldness, lumbago and Parkinson's symptoms].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188608
Ren Zhixia, Chen Shuai, Shi Yingying and 6 more
Genes: NOTCH3
[Clinical and genetic analysis of two unrelated patients with Angelman syndrome and novel UBE3A mutations].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188609
Xu Huihui, Ji Xing, Xu Yan and 4 more
[Influence of CYP2C19 gene polymorphisms on the efficacy of clopidogrel treatment for the prevention of ischemic stroke following coronary stent implantation].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188612
Li Guode, Chen Jingjuan, Xu Zuohang and 5 more
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188615
Ji Xiuqing, Hu Huanran, Wang Yan and 8 more
[Prenatal diagnosis of a tetrasomy 18p case using BACs-on-Beads technology and single nucleotide polymorphism array].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188616
Jiang Huling, Ping Zepeng, Wang Luming and 4 more
Genes: LPIN2, SMCHD1, TGIF1
[SNP array analysis of three cases with partial 21q trisomy].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188617
Zhou Lili, Chen Chong, Zheng Zhaoke and 6 more
[Identification of novel compound heterozygous mutations in the ANTXR2 gene in a Chinese patient with juvenile hyaline fibromatosis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188618
Zhang Yongling, Li Ru, Li Yan and 1 more
Genes: ANTXR2
[Detection and prenatal diagnosis of TOR1A gene mutation in a Chinese family affected with dystonia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188619
Chen Chen, Zhu Chaofeng, Zhao Zhenhua and 2 more
[Analysis of genotype and phenotype of SEC23B gene in a family affected with congenital dyserythropoietic anemia type II].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188620
Li Dongliang, Li Bolun, Qu Shanshan and 4 more
Genes: CDA, HFE
[Prenatal diagnosis of a fetus with Miller-Dieker syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188621
Xu Liangpu, Huang Hailong, Wang Yan and 7 more
[Identification of a novel Bx allele of the ABO blood group].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188624
He Yunlei, Yu Lu, Deng Gang and 2 more
Genes: ABO
[Identification of a novel ABO B(A)07 allele].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188625
Luo Hong, Luo Guangping, Zhang Runqing and 2 more
Genes: ABO
[Polymorphism of RHD gene among RhD negative and D variant blood donors from Qingdao region].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188626
Hu Bin, Feng Zhihui, Zhu Yuli
Genes: RHD
[Association of aggressive behaviors of schizophrenia with short tandem repeats loci].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188627
Yang Chun, Ba Huajie, Tan Xingqi and 3 more
Genes: FGA
[Effect of MTHFR gene on the schizophrenia and its cognitive function].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188628
Wang Weiping, Fan Weixing, Shi Bo and 4 more
Genes: MTHFR
[Association of HSPA1A gene single nucleotide polymorphisms with the development of cervical cancer among ethnic Han Chinese from Yunnan].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188629
Zhang Xinwen, Yan Zhiling, Shi Li and 5 more
[Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2017-12-10 | PMID 29188631
He Shengliang, Du Jing, Liu Fangqi
Genes: FAP, APC, MUTYH
[Correlation between interleukin-10 polymorphisms and susceptibility to chronic periodontitis among Uygur adults in the Moyu area].
Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology | 2017-10-01 | PMID 29188649
Yuhui Zhang, Ping Huang, Jing Lin and 1 more
[Genetic Polymorphisms of SNP Located in the 5' Region of VEGF Gene in Han Population in Guangdong].
Fa yi xue za zhi | 2016-08-01 | PMID 29188666
He W Z, Ma X Y, Xian J J and 5 more
[Review of Second Generation Sequencing and Its Application in Forensic Genetics].
Fa yi xue za zhi | 2016-08-01 | PMID 29188673
Zhang S H, Bian Y N, Zhao Q and 1 more
Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach.
International journal of obesity (2005) | 2018-04-01 | PMID 29188820
Kotnik P, Knapič E, Kokošar J and 4 more
Genes: PYGB, ECE1, GNPDA1
Supplementation of Mussel Peptides Reduces aging Phenotype, Lipid Deposition and Oxidative Stress in D-Galactose-Induce Aging Mice.
The journal of nutrition, health & aging | 2017-01-01 | PMID 29188895
Zhou Y, Xu Q, Dong Y and 3 more
Classification, Morphology, Molecular Pathogenesis, and Outcome of Premalignant Lesions of the Pancreas.
Archives of pathology & laboratory medicine | 2017-12-01 | PMID 29189063
Pittman Meredith E, Rao Rema, Hruban Ralph H
The Updated World Health Organization Glioma Classification: Cellular and Molecular Origins of Adult Infiltrating Gliomas.
Archives of pathology & laboratory medicine | 2017-12-01 | PMID 29189064
Pisapia David J
The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy.
Current gene therapy | 2017-01-01 | PMID 29189152
Zhang Yong, Tian Zhen, Yuan Jiajia and 4 more
Sex Differences in Neuropsychological Test Performance in Alzheimer's Disease and the Influence of the ApoE Genotype.
Alzheimer disease and associated disorders | 2000-01-01 | PMID 29189302
Tensil Maria, Hessler Johannes B, Gutsmiedl Maria and 3 more
Advances in the Genetics and Biology of Pancreatic Cancer.
Cancer journal (Sudbury, Mass.) | 2000-01-01 | PMID 29189326
Aguirre Andrew J, Collisson Eric A
Asthma: personalized and precision medicine.
Current opinion in allergy and clinical immunology | 2018-02-01 | PMID 29189350
Canonica Giorgio W, Ferrando Matteo, Baiardini Ilaria and 4 more
Association of Cardiac Abnormalities to the Frail Phenotype in Cirrhotic Patients on the Waitlist: From the Functional Assessment in Liver Transplantation Study.
Transplantation | 2018-03-01 | PMID 29189486
Puchades Lorena, Chau Stephanie, Dodson John A and 6 more
Successful Nonmyeloablative Allogeneic Stem Cell Transplant in a Child With Emberger Syndrome and GATA2 Mutation.
Journal of pediatric hematology/oncology | 2018-08-01 | PMID 29189513
Rastogi Neha, Abraham Roshini S, Chadha Ritu and 4 more
Genes: GATA2
Somatic PTPN11 Mutation in a Child With Neuroblastoma and Protein Losing Enteropathy.
Journal of pediatric hematology/oncology | 2018-05-01 | PMID 29189514
Obasaju Patience, Brondon Jennifer, Mir Sabina and 3 more
Genes: PTPN11
Common Variant of POC5 Is Associated With the Susceptibility of Adolescent Idiopathic Scoliosis.
Spine | 2018-06-15 | PMID 29189569
Xu Leilei, Sheng Fei, Xia Chao and 4 more
Genes: POC5
A randomized phase II study of S-1 versus capecitabine as first-line chemotherapy in elderly metastatic gastric cancer patients with or without poor performance status: clinical and pharmacogenetic results.
Pharmacogenetics and genomics | 2018-01-01 | PMID 29189588
Kim Mi-Jung, Kong Sun-Young, Nam Byung-Ho and 3 more
VANGL1 Is Not Associated With the Susceptibility of Adolescent Idiopathic Scoliosis in the Chinese Population.
Spine | 2018-05-15 | PMID 29189642
Xu Leilei, Sheng Fei, Xia Chao and 3 more
Genes: VANGL1
Rotavirus Genotypes Circulating in Brazil Before and After the National Rotavirus Vaccine Program: A Review.
The Pediatric infectious disease journal | 2018-03-01 | PMID 29189673
Santos Victor S, Nóbrega Flávia A, Soares Mariana W S and 3 more
Site I Inactivation Impacts Calmodulin Calcium Binding and Activation of Bordetella pertussis Adenylate Cyclase Toxin.
Toxins | 2017-11-30 | PMID 29189743
Johns Christian W, Finley Natosha L
Genes: ACD
Deriving genotypes from RAD-seq short-read data using Stacks.
Nature protocols | 2017-12-01 | PMID 29189774
Rochette Nicolas C, Catchen Julian M
Elevational distribution and morphological attributes of the entomopathogenic fungi from forests of the Qinling Mountains in China.
Applied microbiology and biotechnology | 2018-02-01 | PMID 29189901
Masoudi Abolfazl, Koprowski John Lad, Bhattarai Upendra Raj and 1 more
Genes: TEF
Cell wall biosynthesis impairment affects the budding lifespan of the Saccharomyces cerevisiae yeast.
Biogerontology | 2018-02-01 | PMID 29189912
Molon Mateusz, Woznicka Olga, Zebrowski Jacek
Congenital myasthenic syndrome with episodic apnoea: clinical, neurophysiological and genetic features in the long-term follow-up of 19 patients.
Journal of neurology | 2018-01-01 | PMID 29189923
McMacken Grace, Whittaker Roger G, Evangelista Teresinha and 3 more
Genes: CHAT, RAPSN
Cardiac structure and function in elite Native Hawaiian and Pacific Islander Rugby Football League athletes: an exploratory study.
The international journal of cardiovascular imaging | 2018-05-01 | PMID 29189933
Johnson Christopher, Forsythe Lynsey, Somauroo John and 3 more
Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.
Familial cancer | 2018-10-01 | PMID 29189962
Malik Salim S, Lythgoe Mark P, McPhail Mark and 1 more
Genes: MCC
Association of SIRT1 gene polymorphism and its expression for the risk of alcoholic fatty liver disease in the Han population.
Hepatology international | 2018-01-01 | PMID 29189974
Hou Yeting, Su Bingzhong, Chen Ping and 4 more
Genes: SIRT1
Associations between ALDH1A1 polymorphisms, alcohol consumption, and mortality among Hispanic and non-Hispanic white women diagnosed with breast cancer: the Breast Cancer Health Disparities Study.
Breast cancer research and treatment | 2018-04-01 | PMID 29190005
Xia Zhiyu, Baumgartner Kathy B, Baumgartner Richard N and 6 more
Relevance of genetic relationship in GWAS and genomic prediction.
Journal of applied genetics | 2018-02-01 | PMID 29190011
Pereira Helcio Duarte, Soriano Viana José Marcelo, Andrade Andréa Carla Bastos and 2 more
Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort.
Genetic testing and molecular biomarkers | 2018-01-01 | PMID 29190129
Kondkar Altaf A, Azad Taif A, Almobarak Faisal A and 5 more
Genes: SIX1, SIX6
FAMILIAL CENTRAL SEROUS CHORIORETINOPATHY.
Retina (Philadelphia, Pa.) | 2019-02-01 | PMID 29190234
van Dijk Elon H C, Schellevis Rosa L, Breukink Myrte B and 8 more
Fibrinolysis shutdown is associated with a fivefold increase in mortality in trauma patients lacking hypersensitivity to tissue plasminogen activator.
The journal of trauma and acute care surgery | 2017-12-01 | PMID 29190254
Moore Hunter B, Moore Ernest E, Huebner Benjamin R and 10 more
Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse.
PloS one | 2017-01-01 | PMID 29190290
Rooney Mary F, Porter Richard K, Katz Lisa M and 1 more
Genes: MSTN, COQ4
A network diffusion approach to inferring sample-specific function reveals functional changes associated with breast cancer.
PLoS computational biology | 2017-11-01 | PMID 29190299
Patkar Sushant, Magen Assaf, Sharan Roded and 1 more
Developmental Connectivity and Molecular Phenotypes of Unique Cortical Projection Neurons that Express a Synapse-Associated Receptor Tyrosine Kinase.
Cerebral cortex (New York, N.Y. : 1991) | 2019-01-01 | PMID 29190358
Kast Ryan J, Wu Hsiao-Huei, Levitt Pat
Genes: MET
Gene-edited MLE-15 Cells as a Model for the Hermansky-Pudlak Syndromes.
American journal of respiratory cell and molecular biology | 2018-05-01 | PMID 29190429
Kook Seunghyi, Qi Aidong, Wang Ping and 4 more
Genes: HPS1
A gapmer aptamer nanobiosensor for real-time monitoring of transcription and translation in single cells.
Biomaterials | 2018-02-01 | PMID 29190498
Wang Shue, Xiao Yuan, Zhang Donna D and 1 more
Advances in sarcoma gene mutations and therapeutic targets.
Cancer treatment reviews | 2018-01-01 | PMID 29190505
Gao Peng, Seebacher Nicole A, Hornicek Francis and 2 more
Genetic determinants of freckle occurrence in the Spanish population: Towards ephelides prediction from human DNA samples.
Forensic science international. Genetics | 2018-03-01 | PMID 29190509
Hernando Barbara, Ibañez Maria Victoria, Deserio-Cuesta Julio Alberto and 3 more
Genes: ASIP, BNC2
Predicted activity of UGT2B7, ABCB1, OPRM1, and COMT using full-gene haplotypes and their association with the CYP2D6-inferred metabolizer phenotype.
Forensic science international. Genetics | 2018-03-01 | PMID 29190510
Wendt Frank R, Sajantila Antti, Budowle Bruce
Genes: ABCB1, COMT, OPRM1
Rare missense coding variants in oxytocin receptor (OXTR) in schizophrenia cases are associated with early trauma exposure, cognition and emotional processing.
Journal of psychiatric research | 2018-02-01 | PMID 29190530
Veras Andre B, Getz Mara, Froemke Robert C and 6 more
Genes: OXTR
Cytokine Gene Polymorphism in Children With Idiopathic Nephrotic Syndrome.
Iranian journal of kidney diseases | 2017-11-01 | PMID 29190601
Midan Dina Abdel Razek, Elhelbawy Nesreen Gamal, Habib Mona Salah El-Din and 2 more
Genes: INS, TNF
Association Between Klotho Gene Polymorphism and Markers of Bone Metabolism in Patients Receiving Maintenance Hemodialysis in Iran.
Iranian journal of kidney diseases | 2017-11-01 | PMID 29190606
Nazarian Aboalfazl, Hasankhani Meisam, Aghajany-Nasab Monireh and 1 more
Four Novel NR5A1 Mutations in 46,XY Gonadal Dysgenesis Patients Including Frameshift Mutations with Altered Subcellular SF-1 Localization.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation | 2017-01-01 | PMID 29190620
Rehkämper Jan, Tewes Ann-Christin, Horvath Judit and 3 more
Genes: SRY
NSCLC Patients Harbouring Rare or Complex EGFR Mutations Are More Often Smokers and Might Not Benefit from First-Line Tyrosine Kinase Inhibitor Therapy.
Respiration; international review of thoracic diseases | 2000-01-01 | PMID 29190621
Kauffmann-Guerrero Diego, Huber Rudolf Maria, Reu Simone and 5 more
Genes: EGFR
Focal Segmental Glomerulosclerosis Associated with Chronic Progressive External Ophthalmoplegia and Mitochondrial DNA A3243G Mutation.
Nephron | 2018-01-01 | PMID 29190634
Narumi Kaori, Mishima Eikan, Akiyama Yukako and 11 more
Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer.
British journal of cancer | 2018-01-01 | PMID 29190637
Nanjo Shigeki, Hata Akito, Okuda Chiyuki and 7 more
Genes: EGFR
Actionable mutations in canine hemangiosarcoma.
PloS one | 2017-01-01 | PMID 29190660
Wang Guannan, Wu Ming, Maloneyhuss Martha A and 4 more
Genes: PLCG1, PTEN
Dual expression of immunoreactive estrogen receptor β and p53 is a potential predictor of regional lymph node metastasis and postoperative recurrence in endometrial endometrioid carcinoma.
PloS one | 2017-01-01 | PMID 29190668
Obata Takeshi, Nakamura Mitsuhiro, Mizumoto Yasunari and 5 more
Hepatic Aryl hydrocarbon Receptor Nuclear Translocator (ARNT) regulates metabolism in mice.
PloS one | 2017-01-01 | PMID 29190746
Scott Christopher H, Cha Kuan-Minn, Ngai Jason and 7 more
Genes: ARNT
Genetic diversity and population structure analysis of spinach by single-nucleotide polymorphisms identified through genotyping-by-sequencing.
PloS one | 2017-01-01 | PMID 29190770
Shi Ainong, Qin Jun, Mou Beiquan and 9 more
InDel marker based genetic differentiation and genetic diversity in traditional rice (Oryza sativa L.) landraces of Chhattisgarh, India.
PloS one | 2017-01-01 | PMID 29190790
Sahu Parmeshwar Kumar, Mondal Suvendu, Sharma Deepak and 3 more
Molecular genetic diversity and population structure of Ethiopian white lupin landraces: Implications for breeding and conservation.
PloS one | 2017-01-01 | PMID 29190792
Atnaf Mulugeta, Yao Nasser, Martina Kyalo and 3 more
Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes.
PloS one | 2017-01-01 | PMID 29190809
Ortega-Moreno Laura, Giráldez Beatriz G, Soto-Insuga Victor and 7 more
Genes: ALG13, ARX, CDKL5, CHD2, GRIN1, KCNQ2, PCDH19, POLG
Whole genome sequencing of Oryza sativa L. cv. Seeragasamba identifies a new fragrance allele in rice.
PloS one | 2017-01-01 | PMID 29190814
Bindusree Ganigara, Natarajan Purushothaman, Kalva Sukesh and 1 more
Reduced functional connectivity of fronto-parietal sustained attention networks in severe childhood abuse.
PloS one | 2017-01-01 | PMID 29190830
Hart Heledd, Lim Lena, Mehta Mitul A and 7 more
Genes: FKBP5, MAOA
[C677T-SNP of methylenetetrahydrofolate reductase gene and breast cancer in Mexican women].
Revista medica del Instituto Mexicano del Seguro Social | 2000-01-01 | PMID 29190865
Calderón-Garcidueñas Ana Laura, Cerda-Flores Ricardo Martín, Castruita-Ávila Ana Lilia and 2 more
Genes: MTHFR
Suppression of phenotype of Escherichia coli mutant defective in farnesyl diphosphate synthase by overexpression of gene for octaprenyl diphosphate synthase.
Bioscience, biotechnology, and biochemistry | 2018-06-01 | PMID 29191106
Takahashi Hiroshi, Aihara Yuta, Ogawa Yukihiro and 5 more
Genes: IPP
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review.
BMC medical genetics | 2017-12-01 | PMID 29191162
Tan Li, Bi Bo, Zhao Peiwei and 4 more
Genes: NDE1
Weighted likelihood inference of genomic autozygosity patterns in dense genotype data.
BMC genomics | 2017-12-01 | PMID 29191164
Blant Alexandra, Kwong Michelle, Szpiech Zachary A and 1 more
Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations.
BMC bioinformatics | 2017-12-01 | PMID 29191167
Broeckx Bart J G, Peelman Luc, Saunders Jimmy H and 2 more
Genetic parameters and expected responses to selection for components of feed efficiency in a Duroc pig line.
Genetics, selection, evolution : GSE | 2017-12-01 | PMID 29191169
Sánchez Juan P, Ragab Mohamed, Quintanilla Raquel and 2 more
A fast indirect method to compute functions of genomic relationships concerning genotyped and ungenotyped individuals, for diversity management.
Genetics, selection, evolution : GSE | 2017-12-01 | PMID 29191178
Colleau Jean-Jacques, Palhière Isabelle, Rodríguez-Ramilo Silvia T and 1 more
Asymptomatic infections with highly polymorphic Chlamydia suis are ubiquitous in pigs.
BMC veterinary research | 2017-12-01 | PMID 29191191
Li Min, Jelocnik Martina, Yang Feng and 14 more
Neurons derived from sporadic Alzheimer's disease iPSCs reveal elevated TAU hyperphosphorylation, increased amyloid levels, and GSK3B activation.
Alzheimer's research & therapy | 2017-12-01 | PMID 29191219
Ochalek Anna, Mihalik Balázs, Avci Hasan X and 13 more
Genes: APP, PSEN1
Performance of MTBDRplus assay in detecting multidrug resistant tuberculosis at hospital level.
BMC research notes | 2017-12-01 | PMID 29191227
Kebede Abebaw, Demisse Daniel, Assefa Meazashwork and 4 more
Functional dissection of Drosophila melanogaster SUUR protein influence on H3K27me3 profile.
Epigenetics & chromatin | 2017-12-01 | PMID 29191233
Posukh Olga V, Maksimov Daniil A, Laktionov Petr P and 2 more
Genes: PCNA
MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development.
Acta neuropathologica communications | 2017-11-30 | PMID 29191246
Hamada Nanako, Iwamoto Ikuko, Tabata Hidenori and 1 more
Pseudopregnancy and aseasonal breeding in dairy goats: genetic basis of fertility and impact on lifetime productivity.
Animal : an international journal of animal bioscience | 2018-09-01 | PMID 29191252
Desire S, Mucha S, Coffey M and 3 more
Screening of Patients at Risk for Familial Pancreatic Cancer: What Is Beneﬁcial?
The Surgical clinics of North America | 2018-02-01 | PMID 29191275
Torphy Robert J, Schulick Richard D
Genome Editing: The Recent History and Perspective in Cardiovascular Diseases.
Journal of the American College of Cardiology | 2017-12-05 | PMID 29191331
Musunuru Kiran
Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis.
Brain & development | 2018-04-01 | PMID 29191363
Brackmann Florian, Coras Roland, Rössler Karl and 3 more
Genes: GFAP
A novel homozygous nonsense mutation in NEFL causes autosomal recessive Charcot-Marie-Tooth disease.
Neuromuscular disorders : NMD | 2018-01-01 | PMID 29191368
Fu Jun, Yuan Yun
Genes: NEFL
A novel cell-based high throughput assay to determine neutralizing antibody titers against circulating strains of rubella virus.
Journal of virological methods | 2018-02-01 | PMID 29191395
Kanbayashi Daiki, Kurata Takako, Takahashi Kazuo and 2 more
The Search for 'Evolution-Proof' Antibiotics.
Trends in microbiology | 2018-06-01 | PMID 29191398
Bell Graham, MacLean Craig
Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.
Matrix biology : journal of the International Society for Matrix Biology | 2018-10-01 | PMID 29191403
Yurchenco Peter D, McKee Karen K, Reinhard Judith R and 1 more
Genes: LAMA2
Successful Repatriation of Breast Cancer Surveillance for High-Risk Women to the UK National Health Service Breast Screening Programme.
Clinical breast cancer | 2018-08-01 | PMID 29191429
McVeigh Terri P, Wiggins Jennifer, Ward Simon and 2 more
Genes: BRCA1, BRCA2
Atopic disorders in CHARGE syndrome: A retrospective study and literature review.
European journal of medical genetics | 2018-04-01 | PMID 29191495
Kong Fang, Martin Donna M
Genes: CHD7
A report of three families with FBN1-related acromelic dysplasias and review of literature for genotype-phenotype correlation in geleophysic dysplasia.
European journal of medical genetics | 2018-04-01 | PMID 29191498
Cheng S W, Luk Ho-Ming, Chu YoYo W Y and 4 more
Genes: FBN1, ADAMTSL2