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 7718 of 10600

A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience | 2018-06-01 | PMID 29604340
Liu Yedan, Guo Ya, Liu Peipei and 6 more
Genes: TCF4
GPS: Identification of disease genes by rank aggregation of multi-genomic scoring schemes.
Genomics | 2019-07-01 | PMID 29604342
Meshkin Alireza, Shakery Azadeh, Masoudi-Nejad Ali
Temporal evolutionary analysis of re-emerging recombinant GII.P16_GII.2 norovirus with acute gastroenteritis in patients from Hubei Province of China, 2017.
Virus research | 2018-04-02 | PMID 29604360
Li Jing, Zhang Ting, Cai Kun and 10 more
Effects of ceftriaxone on hydrocodone seeking behavior and glial glutamate transporters in P rats.
Behavioural brain research | 2018-07-16 | PMID 29604365
Alshehri Fahad S, Hakami Alqassem Y, Althobaiti Yusuf S and 1 more
Recurrently Mutated Genes Differ between Leptomeningeal and Solid Lung Cancer Brain Metastases.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2018-07-01 | PMID 29604399
Li Yingmei, Liu Boxiang, Connolly Ian David and 5 more
Genes: EGFR, KRAS
Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern Indians.
Neuroscience letters | 2018-05-14 | PMID 29604408
Sadhukhan Dipanwita, Das Gautami, Biswas Arindam and 4 more
Genes: FGF20
Role of NT-proANP and NT-proBNP in patients with atrial fibrillation: Association with atrial fibrillation progression phenotypes.
Heart rhythm | 2018-08-01 | PMID 29604419
Büttner Petra, Schumacher Katja, Dinov Borislav and 6 more
Prevalence of mutations in genes associated with isoniazid resistance in Mycobacterium tuberculosis isolates from re-treated smear-positive pulmonary tuberculosis patients: A meta-analysis.
Journal of global antimicrobial resistance | 2018-09-01 | PMID 29604431
Alagappan Chitra, Sunil Shivekar Smita, Brammacharry Usharani and 4 more
Reprint of: Quantitative proteomic analysis reveals that chemotaxis is involved in chlortetracycline resistance of Aeromonas hydrophila.
Journal of proteomics | 2018-05-30 | PMID 29604439
Li Wanxin, Ali Farman, Cai Qilan and 4 more
Changes in methylation within the STK32B promoter are associated with an increased risk for generalized anxiety disorder in adolescents.
Journal of psychiatric research | 2018-07-01 | PMID 29604450
Ciuculete Diana M, Boström Adrian E, Tuunainen Anna-Kaisa and 6 more
PON1 promoter polymorphisms contribute to PCOS susceptibility and phenotypic outcomes in Indian women.
Gene | 2018-06-30 | PMID 29604466
Dadachanji Roshan, Shaikh Nuzhat, Patil Anushree and 2 more
Genes: PON1
Oncogenic RAS: From Its Activation to Its Direct Targeting.
Critical reviews in oncogenesis | 2017-01-01 | PMID 29604905
Zaravinos Apostolos
The Long Evolutionary Journey of Cancer from Ancestor to Modern Humans.
Critical reviews in oncogenesis | 2017-01-01 | PMID 29604908
Carruba Giuseppe, Trosko James E
Yin Yang 1 (YY1): Regulation of Survivin and Its Role In Invasion and Metastasis.
Critical reviews in oncogenesis | 2017-01-01 | PMID 29604934
Galloway Nicholas R, Ball Kathryn F, Stiff TessaRae and 1 more
Deletion of Orai2 augments endogenous CRAC currents and degranulation in mast cells leading to enhanced anaphylaxis.
Cell calcium | 2018-05-01 | PMID 29604961
Tsvilovskyy Volodymyr, Solís-López Alejandra, Schumacher Dagmar and 4 more
A critical appraisal of the role of intracellular Ca2+-signaling pathways in Kawasaki disease.
Cell calcium | 2018-05-01 | PMID 29604968
Bijnens Jeroen, Missiaen Ludwig, Bultynck Geert and 1 more
Genes: ORAI1
Circulating genotypes of Toxoplasma gondii in Northwestern Italy.
Veterinary parasitology | 2018-04-15 | PMID 29605002
Battisti Elena, Zanet Stefania, Trisciuoglio Anna and 2 more
Tongue has higher larval burden of Trichinella spp. than diaphragm in wolverines (Gulo gulo).
Veterinary parasitology | 2018-04-15 | PMID 29605011
Sharma Rajnish, Harms N Jane, Kukka Piia M and 4 more
Genetic Vulnerability of GPCRs: A Call to Action.
Trends in biochemical sciences | 2018-04-01 | PMID 29605062
Liggett Stephen B
Why Functional Traits Do Not Predict Tree Demographic Rates.
Trends in ecology & evolution | 2018-05-01 | PMID 29605086
Yang Jie, Cao Min, Swenson Nathan G
The latent trait of ICD-11 nicotine dependence criteria: Dimensional and categorical phenotypes.
Psychiatry research | 2018-08-01 | PMID 29605101
Castaldelli-Maia João Mauricio, Andrade Laura H, Storr Carla L and 3 more
ALS Genes in the Genomic Era and their Implications for FTD.
Trends in genetics : TIG | 2018-06-01 | PMID 29605155
Nguyen Hung Phuoc, Van Broeckhoven Christine, van der Zee Julie
Genes: ANXA11, CCNF, CHCHD10, MATR3, NEK1, TBK1, TIA1
Systematic Evaluation of Molecular Networks for Discovery of Disease Genes.
Cell systems | 2018-04-25 | PMID 29605183
Huang Justin K, Carlin Daniel E, Yu Michael Ku and 4 more
The effect of using cow genomic information on accuracy and bias of genomic breeding values in a simulated Holstein dairy cattle population.
Journal of dairy science | 2018-06-01 | PMID 29605309
Dehnavi E, Mahyari S Ansari, Schenkel F S and 1 more
Prediction accuracy of direct and indirect approaches, and their relationships with prediction ability of calibration models.
Journal of dairy science | 2018-07-01 | PMID 29605329
Belay T K, Dagnachew B S, Boison S A and 1 more
High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy.
International journal of pediatric otorhinolaryngology | 2018-05-01 | PMID 29605341
Matsushima Kana, Nakano Atsuko, Arimoto Yukiko and 4 more
Genes: GJB2
Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.
International journal of pediatric otorhinolaryngology | 2018-05-01 | PMID 29605349
Ramzan Khushnooda, Al-Owain Mohammed, Huma Rozeena and 4 more
Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatment.
International journal of pediatric otorhinolaryngology | 2018-05-01 | PMID 29605356
Westergaard-Nielsen Marie, Amstrup Tine, Wanscher Jens Højberg and 2 more
Genes: NOG
Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
International journal of pediatric otorhinolaryngology | 2018-05-01 | PMID 29605365
Huang Bangqing, Han Mingyu, Wang Guojian and 4 more
Genes: GJB2
Emberger syndrome: A rare association with hearing loss.
International journal of pediatric otorhinolaryngology | 2018-05-01 | PMID 29605372
Zawawi Faisal, Sokolov Meirav, Mawby Thomas and 3 more
The impact of TNF-α 308G>A gene polymorphism on children's overweight risk and an assessment of biochemical variables: A cross-sectional single-center experience.
Pediatrics and neonatology | 2019-02-01 | PMID 29605384
Mărginean Cristina Oana, Mărginean Claudiu, Iancu Mihaela and 3 more
Genes: TNF, TST
Effects of APOE-ε4 allele load on brain morphology in a cohort of middle-aged healthy individuals with enriched genetic risk for Alzheimer's disease.
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2018-07-01 | PMID 29605385
Cacciaglia Raffaele, Molinuevo José Luis, Falcón Carles and 8 more
Genes: APOE
Venous Thromboembolism in Children with Sickle Cell Disease: A Retrospective Cohort Study.
The Journal of pediatrics | 2018-06-01 | PMID 29605397
Woods Gary M, Sharma Ruchika, Creary Susan and 6 more
Genes: SCD
Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome.
Neurobiology of disease | 2018-07-01 | PMID 29605426
Lovelace Jonathan W, Ethell Iryna M, Binder Devin K and 1 more
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.
Lancet (London, England) | 2018-04-14 | PMID 29605429
Männikkö Roope, Wong Leonie, Tester David J and 18 more
ACSL5 genotype influence on fatty acid metabolism: a cellular, tissue, and whole-body study.
Metabolism: clinical and experimental | 2018-06-01 | PMID 29605434
Rajkumar Abishankari, Liaghati Awa, Chan Jessica and 7 more
Genes: ACSL5
Association between ABCA1 gene polymorphisms and the therapeutic response to donepezil therapy in Han Chinese patients with Alzheimer's disease.
Brain research bulletin | 2018-06-01 | PMID 29605487
Lu Jin, Fu Jianliang, Zhong Yuan and 7 more
Genes: ABCA1, APOE
Apoptosis-Inducing Factor (AIF) in Physiology and Disease: The Tale of a Repented Natural Born Killer.
EBioMedicine | 2018-04-01 | PMID 29605508
Bano Daniele, Prehn Jochen H M
Genes: AIFM1
Epidemiology and molecular characterization of Neisseria lactamica carried in 11-19 years old students in Salvador, Brazil.
International journal of medical microbiology : IJMM | 2018-06-01 | PMID 29605532
Moura Ana Rafaela Silva Simões, Kretz Cécilia Batmalle, Ferreira Ítalo Eustáquio and 7 more
SCN1A rs3812718 polymorphism is associated with epilepsy: An updated meta-analysis.
Epilepsy research | 2018-05-01 | PMID 29605548
Zhi Haiyang, Wu Changan, Yang Ziqing
Rapid phenotypic methods to improve the diagnosis of bacterial bloodstream infections: meeting the challenge to reduce the time to result.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases | 2018-09-01 | PMID 29605563
Dubourg G, Lamy B, Ruimy R
Genetic variations in key inflammatory cytokines exacerbates the risk of diabetic nephropathy by influencing the gene expression.
Gene | 2018-06-30 | PMID 29605608
Hameed Iqra, Masoodi Shariq R, Malik Perveez A and 3 more
Genes: TNF
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review.
Seizure | 2018-04-01 | PMID 29605618
Tian Wo-Tu, Liu Xiao-Li, Xu Yang-Qi and 7 more
Genes: SCARB2
B-factor-saturation mutagenesis as a strategy to increase the thermostability of α-L-rhamnosidase from Aspergillus terreus.
Journal of biotechnology | 2018-06-10 | PMID 29605638
Ge Lin, Li Dongdong, Wu Tao and 4 more
Genome sequencing analysis of liver cancer for precision medicine.
Seminars in cancer biology | 2019-04-01 | PMID 29605648
Nakagawa Hidewaki, Fujita Masashi, Fujimoto Akihiro
Genomic, Recombinational and Phylogenetic Characterization of Global Feline Herpesvirus 1 Isolates.
Virology | 2018-05-01 | PMID 29605685
Lewin Andrew C, Kolb Aaron W, McLellan Gillian J and 4 more
HLA-inferred extended haplotype disparity level is more relevant than the level of HLA mismatch alone for the patients survival and GvHD in T cell-replate hematopoietic stem cell transplantation from unrelated donor.
Human immunology | 2018-06-01 | PMID 29605688
Nowak Jacek, Nestorowicz Klaudia, Graczyk-Pol Elzbieta and 46 more
HLA-G mediated immune regulation is impaired by a single amino acid exchange in the alpha 2 domain.
Human immunology | 2018-06-01 | PMID 29605689
Celik Alexander A, Simper Gwendolin S, Huyton Trevor and 2 more
Lack of evidence of association between IFNG and IL28B polymorphisms and QuantiFERON-CMV test results in seropositive transplant patients.
Human immunology | 2018-06-01 | PMID 29605690
Aguado Rocío, Páez-Vega Aurora, Agüera María L and 11 more
Genes: IFNG
Phenotypic spectrum in families with mesial temporal lobe epilepsy probands.
Seizure | 2018-05-01 | PMID 29605745
Cvetkovska Emilija, Kuzmanovski Igor, Babunovska Marija and 3 more
Genomic changes in an attenuated genotype I Japanese encephalitis virus and comparison with virulent parental strain.
Virus genes | 2018-06-01 | PMID 29605839
Zhou Yuyong, Wu Rui, Feng Yao and 9 more
Targeted Gene Deletion in Cordyceps militaris Using the Split-Marker Approach.
Molecular biotechnology | 2018-05-01 | PMID 29605840
Lou HaiWei, Ye ZhiWei, Yun Fan and 4 more
Induction of a central memory and stem cell memory phenotype in functionally active CD4+ and CD8+ CAR T cells produced in an automated good manufacturing practice system for the treatment of CD19+ acute lymphoblastic leukemia.
Cancer immunology, immunotherapy : CII | 2018-07-01 | PMID 29605883
Blaeschke Franziska, Stenger Dana, Kaeuferle Theresa and 7 more
Genes: TNF
EPHX1 rs1051740 T>C (Tyr113His) is strongly associated with acute myeloid leukemia and KMT2A rearrangements in early age.
Archives of toxicology | 2018-06-01 | PMID 29605894
Brisson Gisele Dallapicola, de Almeida Lopes Bruno, Andrade Francianne Gomes and 6 more
Genes: EPHX1, GSTM1, GSTT1, MPO, NQO1
GNAS-mutated carcinoma arising from gastric foveolar metaplasia in the duodenum after 9 years of observation.
Clinical journal of gastroenterology | 2018-10-01 | PMID 29605945
Matsuo Yasumasa, Yamamoto Hiroyuki, Sato Yoshinori and 7 more
Genes: GNAS
Medical management of meningioma in the era of precision medicine.
Neurosurgical focus | 2018-04-01 | PMID 29606052
Gupta Saksham, Bi Wenya Linda, Dunn Ian F
High-grade meningiomas: biology and implications.
Neurosurgical focus | 2018-04-01 | PMID 29606053
Bi Wenya Linda, Prabhu Vikram C, Dunn Ian F
Genes: AKT1, BAP1, KLF4, SMARCB1, SMARCE1, SMO, SUFU, TERT
DNA Methylation variability among individuals is related to CpGs cluster density and evolutionary signatures.
BMC genomics | 2018-04-02 | PMID 29606093
Palumbo Domenico, Affinito Ornella, Monticelli Antonella and 1 more
Molecular epidemiology and temporal evolution of norovirus associated with acute gastroenteritis in Amazonas state, Brazil.
BMC infectious diseases | 2018-04-02 | PMID 29606095
Hernandez Juliana Merces, Silva Luciana Damascena, Junior Edivaldo Costa Sousa and 5 more
Successful production of genome-edited rats by the rGONAD method.
BMC biotechnology | 2018-04-02 | PMID 29606116
Kobayashi Tomoe, Namba Masumi, Koyano Takayuki and 4 more
Polymorphism of the GLIS3 gene in a Caucasian population and among individuals with carbohydrate metabolism disorders in Russia.
BMC research notes | 2018-04-02 | PMID 29606121
Shakhtshneider E V, Mikhailova S V, Ivanoshchuk D E and 5 more
Genes: GLIS3
FTO variant is not associated with osteoarthritis in the Chinese Han population: replication study for a genome-wide association study identified risk loci.
Journal of orthopaedic surgery and research | 2018-04-02 | PMID 29606151
Dai Jin, Ying Pu, Shi Dongquan and 9 more
Genes: FTO
Review: The variability of the eating quality of beef can be reduced by predicting consumer satisfaction.
Animal : an international journal of animal bioscience | 2018-11-01 | PMID 29606159
Bonny S P F, Hocquette J-F, Pethick D W and 6 more
Echinococcus granulosus genotypes in Iran: a systematic review.
Journal of helminthology | 2019-03-01 | PMID 29606162
Khademvatan S, Majidiani H, Foroutan M and 3 more
Genetic mapping of a lobed-leaf gene associated with salt tolerance in Brassica napus L.
Plant science : an international journal of experimental plant biology | 2018-04-01 | PMID 29606219
Zhang Yan, Xu Aixia, Lang Lina and 7 more
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
American journal of human genetics | 2018-04-05 | PMID 29606300
Sang Qing, Li Bin, Kuang Yanping and 14 more
Genes: WEE2
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
American journal of human genetics | 2018-04-05 | PMID 29606301
Dong Frederick N, Amiri-Yekta Amir, Martinez Guillaume and 18 more
Genes: CFAP69
Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.
American journal of human genetics | 2018-04-05 | PMID 29606302
Blackburn Patrick R, Xu Zhi, Tumelty Kathleen E and 16 more
Genes: AEBP1
PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.
American journal of human genetics | 2018-04-05 | PMID 29606303
Verma Anurag, Lucas Anastasia, Verma Shefali S and 8 more
Nuclear Mechanopathology and Cancer Diagnosis.
Trends in cancer | 2018-04-01 | PMID 29606315
Uhler Caroline, Shivashankar G V
Gene Polymorphisms in the CCL5/CCR5 Pathway as a Genetic Biomarker for Outcome and Hand-Foot Skin Reaction in Metastatic Colorectal Cancer Patients Treated With Regorafenib.
Clinical colorectal cancer | 2018-06-01 | PMID 29606345
Suenaga Mitsukuni, Schirripa Marta, Cao Shu and 17 more
Genes: CCL5, CCR5, CCL3, CCL4
Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.
Reproductive biomedicine online | 2018-06-01 | PMID 29606347
Wang Xueqian, Song Di, Mykytenko Dmytro and 19 more
Genes: PADI6, TLE6
Usefulness of Genetic Study by Next-generation Sequencing in High-risk Arrhythmogenic Cardiomyopathy.
Revista espanola de cardiologia (English ed.) | 2018-12-01 | PMID 29606362
Ruiz Salas Amalio, Peña Hernández José, Medina Palomo Carmen and 9 more
Nuclease-free Adeno-Associated Virus-Mediated Il2rg Gene Editing in X-SCID Mice.
Molecular therapy : the journal of the American Society of Gene Therapy | 2018-05-02 | PMID 29606506
Hiramoto Takafumi, Li Li B, Funk Sarah E and 2 more
Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands.
Neuromuscular disorders : NMD | 2018-05-01 | PMID 29606556
Stunnenberg B C, Raaphorst J, Deenen J C W and 10 more
Genes: CLCN1, KCNJ2
Structural Basis of Transcription Inhibition by Fidaxomicin (Lipiarmycin A3).
Molecular cell | 2018-04-05 | PMID 29606590
Lin Wei, Das Kalyan, Degen David and 20 more
A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel.
Structure (London, England : 1993) | 2018-05-01 | PMID 29606593
Johnson Christopher N, Potet Franck, Thompson Matthew K and 6 more
Growth advantage of Escherichia coli O104:H4 strains on 5-N-acetyl-9-O-acetyl neuraminic acid as a carbon source is dependent on heterogeneous phage-Borne nanS-p esterases.
International journal of medical microbiology : IJMM | 2018-06-01 | PMID 29606600
Saile Nadja, Schwarz Lisa, Eißenberger Kristina and 3 more
Heterogeneity of Human Breast Stem and Progenitor Cells as Revealed by Transcriptional Profiling.
Stem cell reports | 2018-05-08 | PMID 29606612
Colacino Justin A, Azizi Ebrahim, Brooks Michael D and 11 more
Genes: SOX2, TWIST1, ZEB2
Promoting Myelin Repair through In Vivo Neuroblast Reprogramming.
Stem cell reports | 2018-05-08 | PMID 29606615
El Waly Bilal, Cayre Myriam, Durbec Pascale
Genes: OLIG2, SOX10
Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived Microglia.
Stem cell reports | 2018-04-10 | PMID 29606617
Brownjohn Philip W, Smith James, Solanki Ravi and 5 more
Genes: TREM2
PPARgamma-2 and ADRB3 polymorphisms in connective tissue diseases and lipid disorders.
Clinical interventions in aging | 2018-01-01 | PMID 29606859
Grygiel-Górniak Bogna, Ziółkowska-Suchanek Iwona, Kaczmarek Elżbieta and 3 more
Genes: ADRB3
Cigarette smoke exposure promotes differentiation of CD4+ T cells toward Th17 cells by CD40-CD40L costimulatory pathway in mice.
International journal of chronic obstructive pulmonary disease | 2018-01-01 | PMID 29606863
Liang Yi, Shen Ying, Kuang Liangjian and 5 more
Noninvasive evaluation of the migration effect of transplanted endothelial progenitor cells in ischemic muscle using a multimodal imaging agent.
International journal of nanomedicine | 2018-01-01 | PMID 29606873
Peng Xingui, Li Cong, Bai Yingying and 5 more
Genetic Testing Preferences of Individuals in Families with Essential Tremor.
Tremor and other hyperkinetic movements (New York, N.Y.) | 2018-01-01 | PMID 29607242
Naranjo Kelly V, Park Jemin, Chen Karen P and 4 more
Hereditary Myoclonus Dystonia: A Novel SGCE Variant and Phenotype Including Intellectual Disability.
Tremor and other hyperkinetic movements (New York, N.Y.) | 2018-01-01 | PMID 29607243
Coughlin David G, Bardakjian Tanya M, Spindler Meredith and 1 more
Genes: SGCE
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.
BioMed research international | 2018-01-01 | PMID 29607327
Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M and 9 more
Population pharmacokinetics of voriconazole and CYP2C19 polymorphisms for optimizing dosing regimens in renal transplant recipients.
British journal of clinical pharmacology | 2018-07-01 | PMID 29607533
Lin Xiao-Bin, Li Zi-Wei, Yan Miao and 9 more
Arabidopsis thaliana expressing PbBSMT, a gene encoding a SABATH-type methyltransferase from the plant pathogenic protist Plasmodiophora brassicae, show leaf chlorosis and altered host susceptibility.
Plant biology (Stuttgart, Germany) | 2019-01-01 | PMID 29607585
Bulman S, Richter F, Marschollek S and 3 more
Differences Between APOE Carriers and Non-APOE Carriers on Neurocognitive Tests: Jensen Effects?
American journal of Alzheimer's disease and other dementias | 2018-09-01 | PMID 29607654
Nijenhuis Jan Te, Choi Kyu Yeong, Choi Yu Yong and 4 more
Genes: APOE
Variations in mating-type-like (MTL) loci direct PCR-based tracking of Zygosaccharomyces strains formed by mating.
The Journal of general and applied microbiology | 2018-07-23 | PMID 29607877
Ogata Tomoo, Kuroki Katsuaki, Ito Koki and 2 more
Genetic variation and structure of Ubame oak, Quercus phillyraeoides, in Japan revealed by chloroplast DNA and nuclear microsatellite markers.
Genes & genetic systems | 2018-09-15 | PMID 29607879
Harada Ko, Dwiyanti Fifi Gus, Liu Huan-Zhen and 3 more
Association analysis of NUCKS1 and INPP5K polymorphism with Parkinson's disease.
Genes & genetic systems | 2018-09-15 | PMID 29607885
Zhu Wenqing, Luo Xiaoguang, Adnan Atif and 5 more
Genes: NUCKS1
Estimating the Asymptomatic Ratio of Norovirus Infection During Foodborne Outbreaks With Laboratory Testing in Japan.
Journal of epidemiology | 2018-09-05 | PMID 29607886
Miura Fuminari, Matsuyama Ryota, Nishiura Hiroshi
[CADASIL with cysteine-sparing NOTCH3 mutation manifesting as dissociated progression between cognitive impairment and brain image findings in 3 years: A case report].
Rinsho shinkeigaku = Clinical neurology | 2018-04-25 | PMID 29607917
Tachiyama Keisuke, Shiga Yuji, Shimoe Yutaka and 3 more
Genes: NOTCH3
Fluorescence Coupled with Macro and Microscopic Examinations of Morphological Phenotype Give Key Characteristics for Identification of Crude Drugs Derived from Scorpions.
Biological & pharmaceutical bulletin | 2018-01-01 | PMID 29607923
Tokumoto Hiroko, Shimomura Hiroko, Hakamatsuka Takashi and 2 more
Characterization of the SN35N Strain-Specific Exopolysaccharide Encoded in the Whole Circular Genome of a Plant-Derived Lactobacillus plantarum.
Biological & pharmaceutical bulletin | 2018-01-01 | PMID 29607926
Noda Masafumi, Shiraga Masaya, Kumagai Takanori and 2 more
Clinical Characteristics, Phenotype of Lipodystrophy and a Genetic Analysis of Six Diabetic Japanese Women with Familial Partial Lipodystrophy in a Diabetic Outpatient Clinic.
Internal medicine (Tokyo, Japan) | 2018-08-15 | PMID 29607946
Iwanishi Masanori, Ito-Kobayashi Jun, Washiyama Miki and 2 more
Genes: LMNA, PPARG
Expression of EMT inducers integrin-linked kinase (ILK) and ZEB1 in phyllodes breast tumors is associated with aggressive phenotype.
Histology and histopathology | 2018-09-01 | PMID 29608014
Akrida Ioanna, Nikou Sofia, Gyftopoulos Konstantinos and 5 more
Genes: ILK, ZEB1
Muscle-restricted nuclear receptor interaction protein knockout causes motor neuron degeneration through down-regulation of myogenin at the neuromuscular junction.
Journal of cachexia, sarcopenia and muscle | 2018-08-01 | PMID 29608040
Chen Hsin-Hsiung, Tsai Li-Kai, Liao Kuan-Yu and 7 more