[Parathyroid cancer].
Vnitrni lekarstvi | 2000-01-01 | PMID 28334546
Ságová Ivana, Stančík Matej, Kentoš Peter and 4 more
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 7286 of 10600
The NCAM1 gene set is linked to depressive symptoms and their brain structural correlates in healthy individuals.
Journal of psychiatric research | 2017-08-01 | PMID 28334615
Petrovska Jana, Coynel David, Fastenrath Matthias and 11 more
Genes: NCAM1
E3 Ubiquitin Ligase Cbl-b Prevents Tumor Metastasis by Maintaining the Epithelial Phenotype in Multiple Drug-Resistant Gastric and Breast Cancer Cells.
Neoplasia (New York, N.Y.) | 2017-04-01 | PMID 28334634
Xu Ling, Zhang Ye, Qu Xiujuan and 12 more
Genes: EGFR, ZEB1
Combining Real-Time COLD- and MAMA-PCR TaqMan Techniques to Detect and Quantify R201 GNAS Mutations in the McCune-Albright Syndrome .
Hormone research in paediatrics | 2017-01-01 | PMID 28334704
de Sanctis Luisa, Galliano Ilaria, Montanari Paola and 3 more
Genes: GNAS
New Genetic Diagnoses of Short Stature Provide Insights into Local Regulation of Childhood Growth .
Hormone research in paediatrics | 2017-01-01 | PMID 28334714
Andrade Anenisia C, Jee Youn Hee, Nilsson Ola
Predominance of G9P[4] Rotavirus from Children with Acute Gastroenteritis in Northwestern Mexico.
Intervirology | 2016-01-01 | PMID 28334725
Felix-Valenzuela Leticia, Cooley-García Dora Patricia, Cano-Rangel Manuel Alberto and 2 more
Disease correction by AAV-mediated gene therapy in a new mouse model of mucopolysaccharidosis type IIID.
Human molecular genetics | 2017-04-15 | PMID 28334745
Roca Carles, Motas Sandra, Marcó Sara and 12 more
Genes: GNS
A Newborn with Transient Diabetes Mellitus Accompanied by Ketoacidosis Attributable to a ZFP57 Mutation.
Journal of tropical pediatrics | 2017-10-01 | PMID 28334746
Iyigun Fatma, Ozcan Beyza, Kulali Ferit and 4 more
Genes: ZFP57
CTG repeat-targeting oligonucleotides for down-regulating Huntingtin expression.
Nucleic acids research | 2017-05-19 | PMID 28334749
Zaghloul Eman M, Gissberg Olof, Moreno Pedro M D and 8 more
Genes: HTT
ATP13A2/PARK9 regulates endo-/lysosomal cargo sorting and proteostasis through a novel PI(3, 5)P2-mediated scaffolding function.
Human molecular genetics | 2017-05-01 | PMID 28334751
Demirsoy S, Martin S, Motamedi S and 7 more
Highly efficient biallelic genome editing of human ES/iPS cells using a CRISPR/Cas9 or TALEN system.
Nucleic acids research | 2017-05-19 | PMID 28334759
Takayama Kazuo, Igai Keisuke, Hagihara Yasuko and 7 more
Genes: RAD51
Golgi-retained Cx32 mutants interfere with gene addition therapy for CMT1X.
Human molecular genetics | 2017-05-01 | PMID 28334782
Kyriakoudi Styliana, Sargiannidou Irene, Kagiava Alexia and 2 more
Genes: GJB1
Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development.
Human molecular genetics | 2017-05-15 | PMID 28334784
Kapoor Ashish, Auer Dallas R, Lee Dongwon and 2 more
Amino acid substitution equivalent to human chorea-acanthocytosis I2771R in yeast Vps13 protein affects its binding to phosphatidylinositol 3-phosphate.
Human molecular genetics | 2017-04-15 | PMID 28334785
Rzepnikowska Weronika, Flis Krzysztof, Kaminska Joanna and 4 more
GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians.
Human molecular genetics | 2017-07-01 | PMID 28334792
Nongmaithem Suraj S, Joglekar Charudatta V, Krishnaveni Ghattu V and 10 more
Genes: FUT6, CUBN, FUT2, MMAA, TCN1, TCN2
Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy.
Human molecular genetics | 2017-05-01 | PMID 28334793
Johnstone Devon L, Nguyen Thi-Tuyet-Mai, Murakami Yoshiko and 15 more
Genes: PIGP, GPI
A critical role of Hrd1 in the regulation of optineurin degradation and aggresome formation.
Human molecular genetics | 2017-05-15 | PMID 28334804
Mao Jiahui, Xia Qin, Liu Chunfeng and 3 more
Genes: OPTN
Allele-specific quantitative proteomics unravels molecular mechanisms modulated by cis-regulatory PPARG locus variation.
Nucleic acids research | 2017-04-07 | PMID 28334807
Lee Heekyoung, Qian Kun, von Toerne Christine and 16 more
Genes: PPARG, RING1, RYBP
Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.
Human molecular genetics | 2017-04-15 | PMID 28334814
Zhu Zezhang, Xu Leilei, Leung-Sang Tang Nelson and 13 more
Genes: TNIK, LBX1, MAGI1, MEIS1
High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds.
Human molecular genetics | 2017-03-01 | PMID 28334820
Ament Seth A, Pearl Jocelynn R, Grindeland Andrea and 20 more
Genes: HTT
Predicting the impact of non-coding variants on DNA methylation.
Nucleic acids research | 2017-06-20 | PMID 28334830
Zeng Haoyang, Gifford David K
AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expression.
Human molecular genetics | 2017-05-15 | PMID 28334834
Gicquel Evelyne, Maizonnier Natacha, Foltz Steven J and 6 more
Genes: FKRP
A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction.
Brain : a journal of neurology | 2017-04-01 | PMID 28334843
Lopez Ana, Lee Suzee E, Wojta Kevin and 16 more
Genes: MAPT
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.
Nucleic acids research | 2017-06-02 | PMID 28334849
Gatto Sole, Gagliardi Miriam, Franzese Monica and 10 more
Genes: PTPRC
Aicardi-Goutières syndrome protein TREX1 suppresses L1 and maintains genome integrity through exonuclease-independent ORF1p depletion.
Nucleic acids research | 2017-05-05 | PMID 28334850
Li Peng, Du Juan, Goodier John L and 5 more
Genes: TREX1
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.
Brain : a journal of neurology | 2017-04-01 | PMID 28334855
Perez Yonatan, Shorer Zamir, Liani-Leibson Keren and 13 more
Genetic regulation of gene expression in the epileptic human hippocampus.
Human molecular genetics | 2017-05-01 | PMID 28334860
Mirza Nasir, Appleton Richard, Burn Sasha and 11 more
Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice.
Human molecular genetics | 2017-06-01 | PMID 28334861
Marcos Séverine, Monnier Carine, Rovira Xavier and 5 more
Genes: PLXNA1
Structure of human POFUT1, its requirement in ligand-independent oncogenic Notch signaling, and functional effects of Dowling-Degos mutations.
Glycobiology | 2017-08-01 | PMID 28334865
McMillan Brian J, Zimmerman Brandon, Egan Emily D and 4 more
Genes: POFUT1
Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease.
Human molecular genetics | 2017-05-01 | PMID 28334871
Segal-Salto Michal, Hansson Karin, Sapir Tamar and 6 more
Genes: PPT1
Alternative DNA structure formation in the mutagenic human c-MYC promoter.
Nucleic acids research | 2017-05-05 | PMID 28334873
Del Mundo Imee Marie A, Zewail-Foote Maha, Kerwin Sean M and 1 more
Genes: MYC
Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders.
Human molecular genetics | 2017-05-15 | PMID 28334874
Zhang Ling, Wang Jingmin, Zhang Cheng and 13 more
Genes: PLP1
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.
Human molecular genetics | 2017-05-15 | PMID 28334876
Arts Florence A, Sciot Raf, Brichard Bénédicte and 13 more
Genes: PDGFRB
High expression of IRE1 in lung adenocarcinoma is associated with a lower rate of recurrence.
Japanese journal of clinical oncology | 2017-06-01 | PMID 28334878
Sakatani Toshio, Maemura Keita, Hiyama Noriko and 8 more
Genes: EGFR
Avoidance of APOBEC3B-induced mutation by error-free lesion bypass.
Nucleic acids research | 2017-05-19 | PMID 28334887
Hoopes James I, Hughes Amber L, Hobson Lauren A and 3 more
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Human molecular genetics | 2017-05-01 | PMID 28334899
Spracklen Cassandra N, Chen Peng, Kim Young Jin and 111 more
Genes: APOBEC1, BPTF, FGFR2, NCOA2, NID2, PDGFC, PTGDR
MERTK rs4374383 variant predicts incident nonalcoholic fatty liver disease and diabetes: role of mononuclear cell activation and adipokine response to dietary fat.
Human molecular genetics | 2017-05-01 | PMID 28334911
Musso Giovanni, Cassader Maurizio, De Michieli Franco and 13 more
Genes: MERTK
TDP-43 mutations causing amyotrophic lateral sclerosis are associated with altered expression of RNA-binding protein hnRNP K and affect the Nrf2 antioxidant pathway.
Human molecular genetics | 2017-05-01 | PMID 28334913
Moujalled Diane, Grubman Alexandra, Acevedo Karla and 14 more
Clinical utility of a self-administered questionnaire for assessment of hereditary gynecologic cancer.
Japanese journal of clinical oncology | 2017-05-01 | PMID 28334914
Masuda Kenta, Hirasawa Akira, Irie-Kunitomi Haruko and 10 more
Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Human molecular genetics | 2017-06-01 | PMID 28334922
Mishra Vikas, Karumuri Bharat K, Gautier Nicole M and 6 more
Rgf1p (Rho1p GEF) is required for double-strand break repair in fission yeast.
Nucleic acids research | 2017-05-19 | PMID 28334931
Manjón Elvira, Edreira Tomás, Muñoz Sofía and 1 more
A pseudaminic acid or a legionaminic acid derivative transferase is strain-specifically implicated in the general protein O-glycosylation system of the periodontal pathogen Tannerella forsythia.
Glycobiology | 2017-06-01 | PMID 28334934
Tomek Markus B, Janesch Bettina, Maresch Daniel and 4 more
Genes: HP
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
Human molecular genetics | 2017-05-15 | PMID 28334935
Raffield Laura M, Louie Tin, Sofer Tamar and 17 more
Genes: ABO, TMPRSS6, FADS2, GAB3, GRB2, HFE, NAT2, TFR2
Clinical and genetic characterization of leukoencephalopathies in adults.
Brain : a journal of neurology | 2017-05-01 | PMID 28334938
Lynch David S, Rodrigues Brandão de Paiva Anderson, Zhang Wei Jia and 26 more
Genes: AARS2, NOTCH3
Mutations affecting the transmembrane domain of the LDL receptor: impact of charged residues on the membrane insertion.
Human molecular genetics | 2017-05-01 | PMID 28334946
Strøm Thea Bismo, Laerdahl Jon K, Leren Trond P
Genes: LDLR, EGFR
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα).
Human molecular genetics | 2017-06-01 | PMID 28334947
Pham Duyen H, Tan Chuan C, Homan Claire C and 7 more
Genes: PCDH19, NONO
Downstream targets of GWAS-detected genes for breast, lung, and prostate and colon cancer converge to G1/S transition pathway.
Human molecular genetics | 2017-04-15 | PMID 28334950
Gorlova Olga Y, Demidenko Eugene I, Amos Christopher I and 1 more
DNMT1 mutations found in HSANIE patients affect interaction with UHRF1 and neuronal differentiation.
Human molecular genetics | 2017-04-15 | PMID 28334952
Smets Martha, Link Stephanie, Wolf Patricia and 6 more
Genes: DNMT1, UHRF1, PCNA
Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering.
Human molecular genetics | 2017-05-15 | PMID 28334953
Vogel Ciernia Annie, Pride Michael C, Durbin-Johnson Blythe and 5 more
The Schizosaccharomyces pombe PPR protein Ppr10 associates with a novel protein Mpa1 and acts as a mitochondrial translational activator.
Nucleic acids research | 2017-04-07 | PMID 28334955
Wang Yirong, Yan Jianhua, Zhang Qingzhen and 5 more
PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.
Brain : a journal of neurology | 2017-04-01 | PMID 28334956
Zollo Massimo, Ahmed Mustafa, Ferrucci Veronica and 44 more
Genes: DHH, PRUNE1
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations.
Human molecular genetics | 2017-05-01 | PMID 28334964
Kosfeld Anne, Brand Frank, Weiss Anna-Carina and 16 more
Genes: LIFR, LIF, STAT3
Identification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease.
Human molecular genetics | 2017-06-01 | PMID 28335003
Gallone Giuseppe, Haerty Wilfried, Disanto Giulio and 3 more
Genes: VDR
A platform for functional assessment of large variant libraries in mammalian cells.
Nucleic acids research | 2017-06-20 | PMID 28335006
Matreyek Kenneth A, Stephany Jason J, Fowler Douglas M
Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci.
Human molecular genetics | 2017-05-15 | PMID 28335009
Fullard John F, Giambartolomei Claudia, Hauberg Mads E and 9 more
Genes: SNX19
The synaptic function of parkin.
Brain : a journal of neurology | 2017-09-01 | PMID 28335015
Sassone Jenny, Serratto GiuliaMaia, Valtorta Flavia and 3 more
tRNA-derived small RNAs target transposable element transcripts.
Nucleic acids research | 2017-05-19 | PMID 28335016
Martinez German, Choudury Sarah G, Slotkin R Keith
Genes: AGO1
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation.
Human molecular genetics | 2017-05-01 | PMID 28335032
Yamamoto Yuta, Makiyama Takeru, Harita Takeshi and 16 more
Genes: CALM2, CALM1
LRSAM1-mediated ubiquitylation is disrupted in axonal Charcot-Marie-Tooth disease 2P.
Human molecular genetics | 2017-06-01 | PMID 28335037
Hakonen Johanna E, Sorrentino Vincenzo, Avagliano Trezza Rossella and 8 more
Clinical characteristics and whole exome/transcriptome sequencing of coexisting chronic myeloid leukemia and myelofibrosis.
American journal of hematology | 2017-06-01 | PMID 28335073
Kandarpa Malathi, Wu Yi-Mi, Robinson Dan and 3 more
Genes: BCR, JAK2, ASXL1, BRAF, CALR, GNAS, IDH2, KRAS
Fine mapping of chromosome 5p15.33 identifies novel lung cancer susceptibility loci in Han Chinese.
International journal of cancer | 2017-08-01 | PMID 28335076
Dong Jing, Cheng Yang, Zhu Meng and 13 more
Genes: TERT, TPPP
Identification of new BMP6 pro-peptide mutations in patients with iron overload.
American journal of hematology | 2017-06-01 | PMID 28335084
Piubelli Chiara, Castagna Annalisa, Marchi Giacomo and 12 more
Genes: BMP6, HFE, HAMP, HJV, TFR2
Genetic Polymorphisms Contribute to the Individual Variations of Imatinib Mesylate Plasma Levels and Adverse Reactions in Chinese GIST Patients.
International journal of molecular sciences | 2017-03-13 | PMID 28335376
Liu Jing, Chen Zhiyu, Chen Hanmei and 6 more
Genes: ABCB1, ABCG2
Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in Tanzania.
International journal of molecular sciences | 2017-03-13 | PMID 28335406
Caggiano Serena, Ullmann Nicola, De Vitis Elisa and 17 more
Profile of Polyphenol Compounds of Five Muscadine Grapes Cultivated in the United States and in Newly Adapted Locations in China.
International journal of molecular sciences | 2017-03-14 | PMID 28335440
Wei Zheng, Luo Jianming, Huang Yu and 5 more
Coccolithoviruses: A Review of Cross-Kingdom Genomic Thievery and Metabolic Thuggery.
Viruses | 2017-03-18 | PMID 28335474
Nissimov Jozef I, Pagarete António, Ma Fangrui and 4 more
Genetic Variants Contributing to Colistin Cytotoxicity: Identification of TGIF1 and HOXD10 Using a Population Genomics Approach.
International journal of molecular sciences | 2017-03-18 | PMID 28335481
Eadon Michael T, Hause Ronald J, Stark Amy L and 9 more
Genes: HOXD10, TGIF1
Genomic Loads and Genotypes of Respiratory Syncytial Virus: Viral Factors during Lower Respiratory Tract Infection in Chilean Hospitalized Infants.
International journal of molecular sciences | 2017-03-21 | PMID 28335547
Espinosa Yazmín, San Martín Camila, Torres Alejandro A and 5 more
Virological Surveillance of Influenza A Subtypes Isolated in 2014 from Clinical Outbreaks in Canadian Swine.
Viruses | 2017-03-21 | PMID 28335552
Grgić Helena, Gallant Jackie, Poljak Zvonimir
Global Functional Analysis of Butanol-Sensitive Escherichia coli and Its Evolved Butanol-Tolerant Strain.
Journal of microbiology and biotechnology | 2017-06-28 | PMID 28335589
Jeong Haeyoung, Lee Seung-Won, Kim Sun Hong and 3 more
Prioritizing Natural Product Diversity in a Collection of 146 Bacterial Strains Based on Growth and Extraction Protocols.
Journal of natural products | 2017-03-24 | PMID 28335604
Crüsemann Max, O'Neill Ellis C, Larson Charles B and 6 more
Opportunistic Sampling of Roadkill as an Entry Point to Accessing Natural Products Assembled by Bacteria Associated with Non-anthropoidal Mammalian Microbiomes.
Journal of natural products | 2017-03-24 | PMID 28335605
Motley Jeremy L, Stamps Blake W, Mitchell Carter A and 6 more
Genetic Heterogeneity in Depressive Symptoms Following the Death of a Spouse: Polygenic Score Analysis of the U.S. Health and Retirement Study.
The American journal of psychiatry | 2017-10-01 | PMID 28335623
Domingue Benjamin W, Liu Hexuan, Okbay Aysu and 1 more
Testis-specific ATP synthase peripheral stalk subunits required for tissue-specific mitochondrial morphogenesis in Drosophila.
BMC cell biology | 2017-03-23 | PMID 28335714
Sawyer Eric M, Brunner Elizabeth C, Hwang Yihharn and 14 more
Genomic regions underlying susceptibility to bovine tuberculosis in Holstein-Friesian cattle.
BMC genetics | 2017-03-23 | PMID 28335717
Raphaka Kethusegile, Matika Oswald, Sánchez-Molano Enrique and 7 more
A genetic chronology for the Indian Subcontinent points to heavily sex-biased dispersals.
BMC evolutionary biology | 2017-03-23 | PMID 28335724
Silva Marina, Oliveira Marisa, Vieira Daniel and 13 more
Allelic incompatibility can explain female biased sex ratios in dioecious plants.
BMC genomics | 2017-03-23 | PMID 28335728
Pucholt Pascal, Hallingbäck Henrik R, Berlin Sofia
Highly diverse population of Picornaviridae and other members of the Picornavirales, in Cameroonian fruit bats.
BMC genomics | 2017-03-23 | PMID 28335731
Yinda Claude Kwe, Zell Roland, Deboutte Ward and 8 more
Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways.
BMC genomics | 2017-03-23 | PMID 28335732
Kheirallah Alexander K, de Moor Cornelia H, Faiz Alen and 2 more
Genes: INTS12, GSTCD
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis.
BMC genomics | 2017-03-23 | PMID 28335735
Iorio Andrea, De Angelis Flavio, Di Girolamo Marco and 8 more
Genes: TTR
Steroid-resistant nephrotic syndrome as the initial presentation of nail-patella syndrome: a case of a de novo LMX1B mutation.
BMC nephrology | 2017-03-23 | PMID 28335748
Nakata Tomohiro, Ishida Ryo, Mihara Yuu and 8 more
Genes: NPS
Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder.
BMC medical genetics | 2017-03-23 | PMID 28335750
Tang Fengzhu, Ma Dengke, Wang Yulan and 8 more
Genes: OTOF, GJB2, GJB3
SVR Rates of HCV-infected population under PEG-IFN-α/R treatment in Northwest China.
Virology journal | 2017-03-23 | PMID 28335783
Li Yanhua, Wang Jiuping, Wang Juan and 6 more
Genotype distribution characteristics of multiple human papillomavirus in women from the Taihu River Basin, on the coast of eastern China.
BMC infectious diseases | 2017-03-23 | PMID 28335818
Lu Jing-Fen, Shen Guo-Rong, Li Qiong and 3 more
First establishment of microsatellite markers in clausiliid snails (Mollusca: Gastropoda: Clausiliidae).
BMC research notes | 2017-03-23 | PMID 28335826
Jaksch Katharina, Kruckenhauser Luise, Haring Elisabeth and 1 more
Familial acute necrotizing encephalopathy with RANBP2 mutation: The first report in Northeast Asia.
Brain & development | 2017-08-01 | PMID 28336122
Lee Yun-Jeong, Hwang Su-Kyeong, Lee So Mi and 1 more
Genes: RANBP2
Complete genome sequence of sequential Pandoraea apista isolates from the same cystic fibrosis patient supports a model of chronic colonization with in vivo strain evolution over time.
Diagnostic microbiology and infectious disease | 2017-01-01 | PMID 28336132
Greninger Alexander L, Streithorst Jessica, Golden Jeffrey A and 2 more
High prevalence of non-clonal imipenem-nonsusceptible Enterobacter spp. isolates in Korea and their association with porin down-regulation.
Diagnostic microbiology and infectious disease | 2017-01-01 | PMID 28336135
Lee Ji-Young, Hong Yoon-Kyoung, Lee Haejeong and 1 more
Association analysis of polymorphism in KiSS1 gene with reproductive traits in goats.
Animal reproduction science | 2017-05-01 | PMID 28336267
El-Tarabany Mahmoud S, Zaglool Asmaa W, El-Tarabany Akram A and 1 more
Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studies.
The Lancet. Neurology | 2017-05-01 | PMID 28336296
Wile Daryl J, Agarwal Pankaj A, Schulzer Michael and 19 more
Regulatory role of CCL5 (rs2280789) and CXCL10 (rs56061981) gene polymorphisms on intracellular CCL5 and CXCL10 expression in pulmonary tuberculosis.
Human immunology | 2000-01-01 | PMID 28336310
Singh Brijendra, Anbalagan Selvaraj, Selvaraj Paramasivam
Genes: CXCL10, CCL5
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin gene.
Neuromuscular disorders : NMD | 2017-06-01 | PMID 28336317
Abdalla Ebtesam, Ravenscroft Gianina, Zayed Louay and 2 more
Knockdown of APPL mimics transgenic Aβ induced neurodegenerative phenotypes in Drosophila.
Neuroscience letters | 2017-05-01 | PMID 28336338
Singh Sandeep Kumar, Srivastav Saurabh, Yadav Amarish Kumar and 1 more
Genes: APP
Viral delivered gene therapy to treat catecholaminergic polymorphic ventricular tachycardia (CPVT2) in mouse models.
Heart rhythm | 2017-07-01 | PMID 28336343
Kurtzwald-Josefson Efrat, Yadin Dor, Harun-Khun Shiraz and 6 more
Genes: CASQ2
New real time and conventional RT-PCRs for updated molecular diagnosis of infectious bronchitis virus infection (IBV) in chickens in Egypt associated with frequent co-infections with avian influenza and Newcastle Disease viruses.
Journal of virological methods | 2017-07-01 | PMID 28336367
Naguib Mahmoud M, El-Kady Magdy F, Lüschow Dörte and 7 more
Emergence of norovirus GII.2 and its novel recombination during the gastroenteritis outbreak in Japanese children in mid-2016.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2017-07-01 | PMID 28336428
Thongprachum Aksara, Okitsu Shoko, Khamrin Pattara and 3 more
Insight into stereochemistry of a new IMP allelic variant (IMP-55) metallo-β-lactamase identified in a clinical strain of Acinetobacter baumannii.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2017-07-01 | PMID 28336429
Shakibaie Mohammad Reza, Azizi Omid, Shahcheraghi Fereshteh
Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case report.
Gene | 2017-06-15 | PMID 28336463
Westphal Dominik S, Andres Stephanie, Beitzel Kirsten I and 3 more
Genes: HNRNPU, ZBTB18, AKT3
Novel therapeutic interventions for pseudoachondroplasia.
Bone | 2017-09-01 | PMID 28336490
Posey Karen L, Hecht Jacqueline T
Genes: COMP
Genetic variation and epigenetic modification of the prodynorphin gene in peripheral blood cells in alcoholism.
Progress in neuro-psychopharmacology & biological psychiatry | 2017-06-02 | PMID 28336495
D'Addario Claudio, Shchetynsky Klementy, Pucci Mariangela and 5 more
Genes: PDYN