Biomedical publications with connected research

Gender-Specific Association Between ABCC2 -24C>T SNP and Reduction in Triglycerides in Chilean Patients Treated With Atorvastatin.

Basic & clinical pharmacology & toxicology | 2018-05-01 | PMID 29178257

Prado Yalena, Arencibia Alberto, Zambrano Tomás and 1 more

Genes: ABCC2

Tracing the origins of genotype VIIh Newcastle disease in southern Africa.

Transboundary and emerging diseases | 2018-04-01 | PMID 29178267

Abolnik C, Mubamba C, Wandrag D B R and 4 more

Unmodern Synthesis: Developmental Hierarchies and the Origin of Phenotypes.

BioEssays : news and reviews in molecular, cellular and developmental biology | 2018-01-01 | PMID 29178269

Gawne Richard, McKenna Kenneth Z, Nijhout H Frederik

Evaluation of modafinil as a perpetrator of metabolic drug-drug interactions using a model informed cocktail reaction phenotyping trial protocol.

British journal of clinical pharmacology | 2018-03-01 | PMID 29178272

Rowland Angela, van Dyk Madelé, Warncken David and 3 more

Effect of LSR polymorphism on blood lipid levels and age-specific epistatic interaction with the APOE common polymorphism.

Clinical genetics | 2018-04-01 | PMID 29178324

Xie T, Stathopoulou M G, Akbar S and 4 more

Genes: LSR, APOE

Chemical Constituents of Sweetpotato Genotypes in Relation to Textural Characteristics of Processed French Fries.

Journal of food science | 2018-01-01 | PMID 29178339

Sato Ai, Truong Van-Den, Johanningsmeier Suzanne D and 3 more

Concise Review: The Use of Stem Cells for Understanding and Treating Huntington's Disease.

Stem cells (Dayton, Ohio) | 2018-02-01 | PMID 29178352

Connor Bronwen

Genes: HTT

Multifactorial disease risk calculator: Risk prediction for multifactorial disease pedigrees.

Genetic epidemiology | 2018-03-01 | PMID 29178360

Campbell Desmond D, Li Yiming, Sham Pak C

Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model.

Clinical genetics | 2018-04-01 | PMID 29178422

Gurbuz F, Desai S, Diao F and 12 more

Genes: DCAF17

Gene-based genetic association test with adaptive optimal weights.

Genetic epidemiology | 2018-02-01 | PMID 29178441

Chen Zhongxue, Lu Yan, Lin Tong and 2 more

Pleistocene climatic changes drive diversification across a tropical savanna.

Molecular ecology | 2018-01-01 | PMID 29178445

Potter Sally, Xue Alexander T, Bragg Jason G and 3 more

Phenotype and genotype analysis of a French cohort of 119 patients with CHARGE syndrome.

American journal of medical genetics. Part C, Seminars in medical genetics | 2017-12-01 | PMID 29178447

Legendre Marine, Abadie Véronique, Attié-Bitach Tania and 44 more

Genes: CHD7

Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies.

Genetic epidemiology | 2018-03-01 | PMID 29178451

Song Minsun, Wheeler William, Caporaso Neil E and 2 more

A Single Mutation is Sufficient to Modify the Metal Selectivity and Specificity of a Eukaryotic Manganese Superoxide Dismutase to Encompass Iron.

Chemistry (Weinheim an der Bergstrasse, Germany) | 2018-04-06 | PMID 29178484

Hunter Thérèse, Bonetta Rosalin, Sacco Anthony and 8 more

Predictive accuracy of combined genetic and environmental risk scores.

Genetic epidemiology | 2018-02-01 | PMID 29178508

Dudbridge Frank, Pashayan Nora, Yang Jian

A catch-22: Interleukin-22 and cancer.

European journal of immunology | 2018-01-01 | PMID 29178520

Hernandez Pedro, Gronke Konrad, Diefenbach Andreas

Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans.

Obesity (Silver Spring, Md.) | 2018-01-01 | PMID 29178545

Gao Chuan, Langefeld Carl D, Ziegler Julie T and 11 more

Genes: MAF, GLIS3, PAPPA2, SRFBP1, TBX15

Shared additive genetic variation for alcohol dependence among subjects of African and European ancestry.

Addiction biology | 2019-01-01 | PMID 29178570

Brick Leslie A, Keller Matthew C, Knopik Valerie S and 2 more

Macrophages-common culprit in obesity and asthma.

Allergy | 2018-06-01 | PMID 29178573

Sharma N, Akkoyunlu M, Rabin R L

Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients.

Clinical genetics | 2018-04-01 | PMID 29178603

He L, Pang X, Liu H and 3 more

Genes: OTOA

Diffusion-weighted MRI characteristics associated with prognostic pathological factors and recurrence risk in invasive ER+/HER2- breast cancers.

Journal of magnetic resonance imaging : JMRI | 2018-07-01 | PMID 29178616

Amornsiripanitch Nita, Nguyen Vicky T, Rahbar Habib and 4 more

Comparative genomics of Spiraeoideae-infecting Erwinia amylovora strains provides novel insight to genetic diversity and identifies the genetic basis of a low-virulence strain.

Molecular plant pathology | 2018-07-01 | PMID 29178620

Zeng Quan, Cui Zhouqi, Wang Jie and 9 more

Clinical and genetic characteristics of xeroderma pigmentosum in Nepal.

Journal of the European Academy of Dermatology and Venereology : JEADV | 2018-05-01 | PMID 29178624

Espi P, Parajuli S, Benfodda M and 7 more

Genes: XPC, ERCC2, XPA

A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178636

Lara-Velazquez Montserrat, Perdomo-Pantoja Alexander, Blackburn Patrick R and 3 more

Allelic spectrum of formiminotransferase-cyclodeaminase gene variants in individuals with formiminoglutamic aciduria.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178637

Majumdar Ramanath, Yori Andrew, Rush Peggy W and 7 more

Genes: FTCD

Spectrum of CFTR gene mutations in Ecuadorian cystic fibrosis patients: the second report of the p.H609R mutation.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178639

Ortiz Sofía C, Aguirre Santiago J, Flores Sofía and 3 more

Genes: CFTR

Expanding the mutational spectrum in Johanson-Blizzard syndrome: identification of whole exon deletions and duplications in the UBR1 gene by multiplex ligation-dependent probe amplification analysis.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178640

Sukalo Maja, Schäflein Eva, Schanze Ina and 8 more

Genes: UBR1

The genetic profile of Leber congenital amaurosis in an Australian cohort.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178642

Thompson Jennifer A, De Roach John N, McLaren Terri L and 6 more

Genes: NMNAT1

Role of WNT10A in failure of tooth development in humans and zebrafish.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178643

Yuan Qiuping, Zhao Min, Tandon Bhavna and 10 more

Inherited SHQ1 mutations impair interaction with NAP57/dyskerin, a major target in dyskeratosis congenita.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178645

Bizarro Jonathan, Meier U Thomas

Genes: SHQ1, DKC1

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178646

Konersman Chamindra G, Freyermuth Fernande, Winder Thomas L and 3 more

Genes: TNNT1

Panel-based whole exome sequencing identifies novel mutations in microphthalmia and anophthalmia patients showing complex Mendelian inheritance patterns.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178648

Riera Marina, Wert Ana, Nieto Isabel and 1 more

Genes: OTX2, PAX6, RBP4

The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178649

Eggermann Thomas, Oehl-Jaschkowitz Barbara, Dicks Severin and 7 more

Compound heterozygous CASQ2 mutations and long-term course of catecholaminergic polymorphic ventricular tachycardia.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178653

Josephs Katherine, Patel Kunjan, Janson Christopher M and 2 more

Genes: CASQ2, RYR2, TRDN

RYR1 causing distal myopathy.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178655

Laughlin Ruple S, Niu Zhiyv, Wieben Eric and 1 more

Genes: RYR1

Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Molecular genetics & genomic medicine | 2017-11-01 | PMID 29178656

Wada Yuko, Ohno Seiko, Aiba Takeshi and 1 more

Genes: DSG2, PKP2, DSC2, DSP

Quantification of classical HLA class I mRNA by allele-specific, real-time polymerase chain reaction for most Han individuals.

HLA | 2018-02-01 | PMID 29178661

Pan N, Lu S, Wang W and 7 more

Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.

Clinical & experimental ophthalmology | 2018-07-01 | PMID 29178665

Abed Edoardo, Placidi Giorgio, Campagna Francesca and 7 more

Genes: ABCA4, ERG

Mosaicism in Cutaneous Disorders.

Annual review of genetics | 2017-11-27 | PMID 29178821

Lim Young H, Moscato Zoe, Choate Keith A

Genetic relatedness of Vibrio cholerae isolates within and between households during outbreaks in Dhaka, Bangladesh.

BMC genomics | 2017-11-25 | PMID 29178823

George Christine Marie, Rashid Mahamud, Almeida Mathieu and 14 more

Phylogenetic relationships of cone snails endemic to Cabo Verde based on mitochondrial genomes.

BMC evolutionary biology | 2017-11-25 | PMID 29178825

Abalde Samuel, Tenorio Manuel J, Afonso Carlos M L and 3 more

Genome-wide segregation of single nucleotide and structural variants into single cancer cells.

BMC genomics | 2017-11-25 | PMID 29178827

Easton John, Gonzalez-Pena Veronica, Yergeau Donald and 2 more

ENCoRE: an efficient software for CRISPR screens identifies new players in extrinsic apoptosis.

BMC genomics | 2017-11-25 | PMID 29178829

Trümbach Dietrich, Pfeiffer Susanne, Poppe Manuel and 4 more

Mosaic autosomal aneuploidies are detectable from single-cell RNAseq data.

BMC genomics | 2017-11-25 | PMID 29178830

Griffiths Jonathan A, Scialdone Antonio, Marioni John C

Genome-wide association studies of fertility and calving traits in Brown Swiss cattle using imputed whole-genome sequences.

BMC genomics | 2017-11-25 | PMID 29178833

Frischknecht Mirjam, Bapst Beat, Seefried Franz R and 10 more

Association of variation in the sugarcane transcriptome with sugar content.

BMC genomics | 2017-11-25 | PMID 29178834

Thirugnanasambandam Prathima P, Hoang Nam V, Furtado Agnelo and 2 more

Prevalence of oncogenic human papillomavirus genotypes in patients diagnosed with anogenital malignancies in Botswana.

BMC infectious diseases | 2017-11-25 | PMID 29178840

Rantshabeng Patricia S, Moyo Sikhulile, Moraka Natasha O and 4 more

Prevalence and types of high-risk human papillomaviruses in head and neck cancers from Bangladesh.

BMC cancer | 2017-11-25 | PMID 29178862

Shaikh Mushfiq H, Khan Aminul I, Sadat Anwar and 7 more

A new panel of SNPs to assess thyroid carcinoma risk: a pilot study in a Brazilian admixture population.

BMC medical genetics | 2017-11-25 | PMID 29178884

Dos Santos Isabelle C C, Genre Julieta, Marques Diego and 10 more

The gut mycobiome of the Human Microbiome Project healthy cohort.

Microbiome | 2017-11-25 | PMID 29178920

Nash Andrea K, Auchtung Thomas A, Wong Matthew C and 9 more

Plasmodium falciparum Kelch 13 mutations and treatment response in patients in Hpa-Pun District, Northern Kayin State, Myanmar.

Malaria journal | 2017-11-25 | PMID 29178921

Bonnington Craig A, Phyo Aung Pyae, Ashley Elizabeth A and 6 more

An Msh3 ATPase domain mutation has no effect on MMR function.

BMC research notes | 2017-11-25 | PMID 29178930

Edwards Yasmin

CRISPR/Cas9-mediated targeted chromosome elimination.

Genome biology | 2017-11-24 | PMID 29178945

Zuo Erwei, Huo Xiaona, Yao Xuan and 15 more

A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.

Genome medicine | 2017-11-27 | PMID 29178946

Polimanti Renato, Amstadter Ananda B, Stein Murray B and 18 more

Molecular evolution and invasion pattern of Cryphonectria hypovirus 1 in Europe: Mutation rate, and selection pressure differ between genome domains.

Virology | 2018-01-15 | PMID 29179038

Mlinarec Jelena, Nuskern Lucija, Ježić Marin and 2 more

A hypermorphic antioxidant response element is associated with increased MS4A6A expression and Alzheimer's disease.

Redox biology | 2018-04-01 | PMID 29179108

Lacher Sarah E, Alazizi Adnan, Wang Xuting and 4 more

Genes: NRF1

Radiosensitization with an inhibitor of poly(ADP-ribose) glycohydrolase: A comparison with the PARP1/2/3 inhibitor olaparib.

DNA repair | 2018-01-01 | PMID 29179156

Gravells Polly, Neale James, Grant Emma and 4 more

Genes: PARG, PARP1, PRKDC, RAD51

CNTNAP2 mutations and autosomal dominant epilepsy with auditory features.

Epilepsy research | 2018-01-01 | PMID 29179159

Leonardi Emanuela, Dazzo Emanuela, Aspromonte Maria Cristina and 6 more

Genes: CNTNAP2, LGI1, RELN

Permanently Hypoxic Cell Culture Yields Rat Bone Marrow Mesenchymal Cells with Higher Therapeutic Potential in the Treatment of Chronic Myocardial Infarction.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology | 2017-01-01 | PMID 29179177

Liu Yihua, Yang Xiaoxi, Maureira Pablo and 7 more

VEGF-A/Neuropilin 1 Pathway Confers Cancer Stemness via Activating Wnt/β-Catenin Axis in Breast Cancer Cells.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology | 2017-01-01 | PMID 29179185

Zhang Lansheng, Wang Hongmei, Li Caihong and 4 more

Hybrid Complexes of High and Low Molecular Weight Hyaluronans Highly Enhance HASCs Differentiation: Implication for Facial Bioremodelling.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology | 2017-01-01 | PMID 29179206

Stellavato Antonietta, La Noce Marcella, Corsuto Luisana and 5 more

Genes: LPL

Atypical Neurologic Phenotype and Novel SLC30A10 Mutation in Two Brothers with Hereditary Hypermanganesemia.

Neuropediatrics | 2018-02-01 | PMID 29179235

Gulab Shamshad, Kayyali Husam R, Al-Said Youssef

SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure.

Molecular genetics & genomic medicine | 2018-01-01 | PMID 29179256

Al Zaabi Nuha, Al Menhali Noora, Al-Jasmi Fatma

Genes: SYNJ1

Is the FSHR 2039A>G variant associated with susceptibility to testicular germ cell cancer?

Andrology | 2018-01-01 | PMID 29179257

Bang A K, Busch A S, Almstrup K and 7 more

Genes: FSHR, FSHB

Targeted Base Editing via RNA-Guided Cytidine Deaminases in Xenopus laevis Embryos.

Molecules and cells | 2017-11-30 | PMID 29179261

Park Dong-Seok, Yoon Mijung, Kweon Jiyeon and 3 more

Advances towards Controlling Meiotic Recombination for Plant Breeding.

Molecules and cells | 2017-11-30 | PMID 29179262

Choi Kyuha

[A survey of willingness about genetic counseling and tests in patients of epithelial ovarian cancer].

Zhonghua yi xue za zhi | 2017-11-21 | PMID 29179283

Li L, Qiu L, Wu M

Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis | 2018-03-01 | PMID 29179580

Amara Ahmed, Mrad Meriem, Sayeh Aicha and 5 more

Genes: CAD

In vitro differentiation of progenitor cells isolated from juvenile pig hearts - expression of relevant gene and protein markers.

Scandinavian cardiovascular journal : SCJ | 2018-02-01 | PMID 29179587

Mogensen Simon Limbrecht, Rasmussen Martin Krøyer, Oksbjerg Niels and 2 more

Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians | 2019-05-01 | PMID 29179591

Mehrad-Majd Hassan, Haerian Monir Sadat, Akhtari Javad and 3 more

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).

Channels (Austin, Tex.) | 2018-01-01 | PMID 29179637

Waldner D M, Giraldo Sierra N C, Bonfield S and 5 more

The Hobnail Variant of Papillary Thyroid Carcinoma: Clinical/Molecular Characteristics of a Large Monocentric Series and Comparison with Conventional Histotypes.

Thyroid : official journal of the American Thyroid Association | 2018-01-01 | PMID 29179638

Watutantrige-Fernando Sara, Vianello Federica, Barollo Susi and 11 more

Genes: TERT, BRAF

Cgl2 plays an essential role in cuticular wax biosynthesis in cabbage (Brassica oleracea L. var. capitata).

BMC plant biology | 2017-11-28 | PMID 29179675

Liu Dongming, Tang Jun, Liu Zezhou and 10 more

Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening.

BMC genetics | 2017-11-28 | PMID 29179688

Shraga Roman, Yarnall Sarah, Elango Sonya and 12 more

High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder.

BMC medical genomics | 2017-11-28 | PMID 29179725

Grünblatt Edna, Oneda Beatrice, Ekici Arif B and 6 more

Genes: NRXN1

Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis.

BMC ophthalmology | 2017-11-28 | PMID 29179746

Li Junhua, Feng Yifan, Sung Mi Sun and 2 more

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.

Genome medicine | 2017-11-27 | PMID 29179772

Wilfert Amy B, Sulovari Arvis, Turner Tychele N and 2 more

Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines.

Genome biology | 2017-11-28 | PMID 29179779

Ghosh Rajarshi, Oak Ninad, Plon Sharon E

CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations.

eLife | 2017-11-28 | PMID 29179815

Okuno Hironobu, Renault Mihara Francois, Ohta Shigeki and 11 more

Genes: CHD7

Analysis of the influence of the T393C polymorphism of the GNAS gene on the clinical expression of primary hyperparathyroidism.

Endocrinologia, diabetes y nutricion | 2017-12-01 | PMID 29179855

Piedra María, Berja Ana, Ramos Laura and 4 more

Genes: GNAS, PTH

HPV genotype-specific concordance between EuroArray HPV, Anyplex II HPV28 and Linear Array HPV Genotyping test in Australian cervical samples.

Papillomavirus research (Amsterdam, Netherlands) | 2017-12-01 | PMID 29179874

Cornall Alyssa M, Poljak Marin, Garland Suzanne M and 5 more

Surgical staging identified false HPV-negative cases in a large series of invasive cervical cancers.

Papillomavirus research (Amsterdam, Netherlands) | 2017-12-01 | PMID 29179875

Petry Karl Ulrich, Liebrich Clemens, Luyten Alexander and 2 more

[Genetic analysis of a family with Von Hippel-Lindau syndrome].

Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia | 2000-01-01 | PMID 29179968

Lafuente-Sanchis Aránzazu, Cuevas José M, Alemany Pilar and 2 more

Genes: VHL

Moving Character Displacement beyond Characters Using Contemporary Coexistence Theory.

Trends in ecology & evolution | 2018-02-01 | PMID 29180041

Germain Rachel M, Williams Jennifer L, Schluter Dolph and 1 more

Alpha-Synuclein transgenic mice, h-α-SynL62, display α-Syn aggregation and a dopaminergic phenotype reminiscent of Parkinson's disease.

Behavioural brain research | 2018-02-26 | PMID 29180135

Frahm Silke, Melis Valeria, Horsley David and 8 more

Distinction of intrahepatic metastasis from multicentric carcinogenesis in multifocal hepatocellular carcinoma using molecular alterations.

Human pathology | 2018-02-01 | PMID 29180252

Chianchiano Peter, Pezhouh Maryam Kherad, Kim Amy and 8 more

Genes: TERT

Development of indirect immunofluorescence assay for TCID50 measurement of grass carp reovirus genotype II without cytopathic effect onto cells.

Microbial pathogenesis | 2018-01-01 | PMID 29180293

Wang Qing, Xie Hualiang, Zeng Weiwei and 6 more

Functional analysis of corin protein domains required for PCSK6-mediated activation.

The international journal of biochemistry & cell biology | 2018-01-01 | PMID 29180304

Chen Shenghan, Wang Hao, Li Heng and 2 more

Genes: PCSK6

Dermoscopy and confocal microscopy for metachronous multiple melanomas: morphological, clinical, and molecular correlations.

European journal of dermatology : EJD | 2018-04-01 | PMID 29180316

Colombino Maria, Paliogiannis Panagiotis, Pagliarello Calogero and 11 more

Genes: BRAF, NRAS

Pseudouridine-Free Escherichia coli Ribosomes.

Journal of bacteriology | 2018-02-15 | PMID 29180357

O'Connor Michael, Leppik Margus, Remme Jaanus

Membrane Vesicles Derived from Bordetella bronchiseptica: Active Constituent of a New Vaccine against Infections Caused by This Pathogen.

Applied and environmental microbiology | 2018-02-15 | PMID 29180369

Bottero D, Zurita M E, Gaillard M E and 3 more

Quantifying the Survival of Multiple Salmonella enterica Serovars In Vivo via Massively Parallel Whole-Genome Sequencing To Predict Zoonotic Risk.

Applied and environmental microbiology | 2018-02-15 | PMID 29180370

Vohra Prerna, Bugarel Marie, Turner Frances and 4 more

Generation of Bacteriophage-Insensitive Mutants of Streptococcus thermophilus via an Antisense RNA CRISPR-Cas Silencing Approach.

Applied and environmental microbiology | 2018-02-15 | PMID 29180373

McDonnell Brian, Mahony Jennifer, Hanemaaijer Laurens and 2 more

OsmiR396d Affects Gibberellin and Brassinosteroid Signaling to Regulate Plant Architecture in Rice.

Plant physiology | 2018-01-01 | PMID 29180380

Tang Yongyan, Liu Huanhuan, Guo Siyi and 4 more

Tamm-Horsfall Protein Regulates Mononuclear Phagocytes in the Kidney.

Journal of the American Society of Nephrology : JASN | 2018-03-01 | PMID 29180395

Micanovic Radmila, Khan Shehnaz, Janosevic Danielle and 10 more

The UMOD Locus: Insights into the Pathogenesis and Prognosis of Kidney Disease.

Journal of the American Society of Nephrology : JASN | 2018-03-01 | PMID 29180396

Devuyst Olivier, Pattaro Cristian

Genes: UMOD

ApoL1 Overexpression Drives Variant-Independent Cytotoxicity.

Journal of the American Society of Nephrology : JASN | 2018-03-01 | PMID 29180397

O'Toole John F, Schilling William, Kunze Diana and 7 more

Genes: APOL1

Neural deletion of Sh2b1 results in brain growth retardation and reactive aggression.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2018-04-01 | PMID 29180441

Jiang Lin, Su Haoran, Keogh Julia M and 6 more

A variant of death-receptor 3 associated with rheumatoid arthritis interferes with apoptosis-induction of T cell.

The Journal of biological chemistry | 2018-02-09 | PMID 29180447

Hashiramoto Akira, Konishi Yoshitake, Murayama Koichi and 12 more

Genes: TNF

Ligand-specific conformational transitions and intracellular transport are required for atypical chemokine receptor 3-mediated chemokine scavenging.

The Journal of biological chemistry | 2018-01-19 | PMID 29180449

Montpas Nicolas, St-Onge Geneviève, Nama Nassr and 6 more

Genes: ACKR3, CXCL11, CXCL12