Association of GWAS-Reported Variant rs11196288 near HABP2 with Ischemic Stroke in Chinese Han Population.
Journal of molecular neuroscience : MN | 2017-06-01 | PMID 28501930
Li Shao-Hua, Shi Chang-He, Li Yu-Sheng and 7 more
Genes: HABP2
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 7350 of 10600
Heightened perception of breast cancer risk in young women at risk of familial breast cancer.
Familial cancer | 2018-01-01 | PMID 28501958
Glassey Rachael, O'Connor Moira, Ives Angela and 3 more
Negative control of Candida albicans filamentation-associated gene expression by essential protein kinase gene KIN28.
Current genetics | 2017-12-01 | PMID 28501989
Woolford C A, Lagree K, Aleynikov T and 1 more
Somatic DNA Mutation Analysis.
Methods in molecular biology (Clifton, N.J.) | 2017-01-01 | PMID 28502004
O'Grady Anthony, Cummins Robert
Evolutionary processes in populations of Cryptosporidium inferred from gp60 sequence data.
Parasitology research | 2017-07-01 | PMID 28502018
Garcia-R Juan C, Hayman David T S
The Role of the Broader Autism Phenotype and Environmental Stressors in the Adjustment of Siblings of Children with Autism Spectrum Disorders in Taiwan and the United Kingdom.
Journal of autism and developmental disorders | 2017-08-01 | PMID 28502037
Tsai Hsiao-Wei Joy, Cebula Katie, Fletcher-Watson Sue
UGT1A1 polymorphisms with irinotecan-induced toxicities and treatment outcome in Asians with Lung Cancer: a meta-analysis.
Cancer chemotherapy and pharmacology | 2017-06-01 | PMID 28502040
Chen Xuewei, Liu Liping, Guo Zhihua and 10 more
Different Hippocampus Functional Connectivity Patterns in Healthy Young Adults with Mutations of APP/Presenilin-1/2 and APOEε4.
Molecular neurobiology | 2018-04-01 | PMID 28502043
Zheng Li Juan, Su Yun Yan, Wang Yun Fei and 8 more
Genes: APOE, APP
A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.
Molecular neurobiology | 2018-04-01 | PMID 28502045
Taghavi Shaghayegh, Chaouni Rita, Tafakhori Abbas and 45 more
Genes: PINK1, SYNJ1, VAC14
Dual-specificity tyrosine-regulated kinase 2 is a suppressor and potential prognostic marker for liver metastasis of colorectal cancer.
Cancer science | 2017-08-01 | PMID 28502078
Ito Daisuke, Yogosawa Satomi, Mimoto Rei and 5 more
Genes: DYRK2
Association between cytokine profile and transcription factors produced by T-cell subsets in early- and late-onset pre-eclampsia.
Immunology | 2017-09-01 | PMID 28502089
Ribeiro Vanessa R, Romao-Veiga Mariana, Romagnoli Graziela G and 5 more
The TLR4-TRIF pathway can protect against the development of experimental allergic asthma.
Immunology | 2017-09-01 | PMID 28502093
Shalaby Karim H, Al Heialy Saba, Tsuchiya Kimitake and 6 more
Genes: ICOS, TLR4, TLR2
Identification of somatic TERT promoter mutations in familial nonmedullary thyroid carcinomas.
Clinical endocrinology | 2017-10-01 | PMID 28502101
Marques Inês J, Moura Margarida M, Cabrera Rafael and 9 more
Genes: TERT, BRAF
Functional analysis by minigene assay of putative splicing variants found in Bardet-Biedl syndrome patients.
Journal of cellular and molecular medicine | 2017-10-01 | PMID 28502102
Álvarez-Satta María, Castro-Sánchez Sheila, Pousada Guillermo and 1 more
Genes: ALMS1, ARL6, BBS2, BBS4
Expression of the filaggrin gene in umbilical cord blood predicts eczema risk in infancy: A birth cohort study.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 2017-09-01 | PMID 28502108
Ziyab A H, Ewart S, Lockett G A and 4 more
Genes: FLG
Humanized NOG mice as a model for tuberculosis vaccine-induced immunity: a comparative analysis with the mouse and guinea pig models of tuberculosis.
Immunology | 2017-09-01 | PMID 28502122
Grover Ajay, Troy Amber, Rowe Jenny and 6 more
Genes: NOG
Risk Association between TNF-α-308 G>A and IL-6-174 G/C Polymorphisms and Recurrent Transient Ischemic Attacks.
The Egyptian journal of immunology | 2015-06-01 | PMID 28502144
Salama Hassan, Hammad Enas
Genes: TNF
Study of Interleukin 28B rs12979860 and rs8099917 Polymorphisms and T-helper 1 Response in Hepatitis C Virus Patients.
The Egyptian journal of immunology | 2015-06-01 | PMID 28502145
Ea Rashwan, Aa Ghazy, Ag El-Sheredy and 1 more
Surface Expression and Genetic Variants of Toll-like Receptor 2 in Pulmonary Tuberculosis Patients.
The Egyptian journal of immunology | 2016-01-01 | PMID 28502147
Aboelazm Abeer A, Abd El-Glil Reem R, Elmahdy Mohamed
Genes: TLR2
Serum Anti-TPO and TPO Gene Polymorphism as a Predictive Factor for Hidden Autoimmune Thyroiditis in Patient with Bronchial Asthma and Allergic Rhinitis.
The Egyptian journal of immunology | 2016-01-01 | PMID 28502155
El Shabrawy Reham M, Atta Amal H, Rashad Nearmeen M
Genes: TPO
Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms.
Journal of the American Chemical Society | 2017-05-31 | PMID 28502178
Solinski Amy E, Koval Alexander B, Brzozowski Richard S and 9 more
Investigation of angiogenesis genes with anterior cruciate ligament rupture risk in a South African population.
Journal of sports sciences | 2018-03-01 | PMID 28502223
Rahim Masouda, Hobbs Hayden, van der Merwe Willem and 3 more
Genes: KDR, VEGFA
Molecular analysis and genetic diversity of Aedes albopictus (Diptera, Culicidae) from China.
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis | 2018-05-01 | PMID 28502235
Ruiling Zhang, Peien Leng, Xuejun Wang and 1 more
Genes: FST
Differential analysis of mutations in the Jewish population and their implications for diseases.
Genetics research | 2017-05-15 | PMID 28502252
Einhorn Yaron, Weissglas-Volkov Daphna, Carmi Shai and 3 more
Genes: HGFAC
Within-host interference competition can prevent invasion of rare parasites.
Parasitology | 2018-05-01 | PMID 28502267
Quigley Benjamin J Z, Brown Sam P, Leggett Helen C and 2 more
Atypical teratoid rhabdoid tumor arising in a pleomorphic xanthoastrocytoma: a rare entity.
Clinical neuropathology | 2000-01-01 | PMID 28502320
Uner Meral, Saglam Arzu, Meydan Bilge Can and 2 more
Genes: BRAF
Favorable long-term outcomes of isolated liver transplantation in a child with atypical hemolytic uremic syndrome caused by a novel complement factor H mutation .
Clinical nephrology | 2017-07-01 | PMID 28502324
Cho Heeyeon, Lee Yeonhee
Genes: CFH
Early-Onset Acute Recurrent and Chronic Pancreatitis Is Associated with PRSS1 or CTRC Gene Mutations.
The Journal of pediatrics | 2017-07-01 | PMID 28502372
Giefer Matthew J, Lowe Mark E, Werlin Steven L and 20 more
Genes: CTRC, PRSS1
Acute bronchodilator responses to β2-agonist and anticholinergic agent in COPD: Their different associations with exacerbation.
Respiratory medicine | 2017-06-01 | PMID 28502414
Konno Satoshi, Makita Hironi, Suzuki Masaru and 4 more
Megakaryocytes in Myeloproliferative Neoplasms Have Unique Somatic Mutations.
The American journal of pathology | 2017-07-01 | PMID 28502479
Guo Belinda B, Allcock Richard J, Mirzai Bob and 10 more
Genes: CALR, MPL
Detection of common sequence variations of familial hypercholesterolemia in Taiwan using DNA mass spectrometry.
Journal of clinical lipidology | 2000-01-01 | PMID 28502495
Chiou Kuan-Rau, Charng Min-Ji
The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia.
Journal of clinical lipidology | 2000-01-01 | PMID 28502497
Paquette Martine, Chong Michael, Saavedra Yascara Grisel Luna and 3 more
Lysosomal acid lipase deficiency: A hidden disease among cohorts of familial hypercholesterolemia?
Journal of clinical lipidology | 2000-01-01 | PMID 28502505
Chora Joana Rita, Alves Ana Catarina, Medeiros Ana Margarida and 6 more
Genes: LIPA
Plasma lipoprotein(a) levels in patients with homozygous autosomal dominant hypercholesterolemia.
Journal of clinical lipidology | 2000-01-01 | PMID 28502508
Sjouke Barbara, Yahya Reyhana, Tanck Michael W T and 7 more
Genes: APOB, LDLR, PCSK9
The heterozygous N291S mutation in the lipoprotein lipase gene impairs whole-body insulin sensitivity and affects a distinct set of plasma metabolites in humans.
Journal of clinical lipidology | 2000-01-01 | PMID 28502509
Berg Sofia Mikkelsen, Havelund Jesper, Hasler-Sheetal Harald and 7 more
Preliminary spectrum of genetic variants in familial hypercholesterolemia in Argentina.
Journal of clinical lipidology | 2000-01-01 | PMID 28502510
Bañares Virginia G, Corral Pablo, Medeiros Ana Margarida and 7 more
Genes: APOB
Functional analysis of new 3' untranslated regions genetic variants in genes associated with genetic hypercholesterolemias.
Journal of clinical lipidology | 2000-01-01 | PMID 28502511
Pérez-Campo Flor María, De Castro-Orós Isabel, Noriega Alicia and 7 more
Lysosomal acid lipase deficiency in all siblings of the same parents.
Journal of clinical lipidology | 2000-01-01 | PMID 28502515
Maciejko James J, Anne Premchand, Raza Saleem and 1 more
Genes: LIPA
Mechanisms underlying the early risk to develop anxiety and depression: A translational approach.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology | 2017-06-01 | PMID 28502529
Kalin Ned H
3'-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.
Clinica chimica acta; international journal of clinical chemistry | 2017-08-01 | PMID 28502559
Karthi Sellamuthu, Rajeshwari Mohan, Francis Amirtharaj and 5 more
A case of a novel mutation in HNF1β-related maturity-onset diabetes of the young type 5 with diabetic kidney disease complication in a Chinese family.
Journal of diabetes and its complications | 2017-07-01 | PMID 28502589
Wang Yiting, Zhao Yingwang, Zhang Junlin and 2 more
Genes: ACE, KCNQ1, SORBS1
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
American journal of human genetics | 2017-06-01 | PMID 28502612
Wang Julia, Al-Ouran Rami, Hu Yanhui and 10 more
Partially compromised specification causes stochastic effects on gut development in C. elegans.
Developmental biology | 2017-07-01 | PMID 28502614
Choi Hailey, Broitman-Maduro Gina, Maduro Morris F
RACK-1, a multifaceted regulator is required for C. elegans innate immunity against S. flexneri M9OT infection.
Developmental and comparative immunology | 2017-09-01 | PMID 28502651
Marudhupandiyan Shanmugam, Prithika Udayakumar, Balasubramaniam Boopathi and 1 more
Genotype-guided dosing of warfarin through modeling and simulation.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences | 2017-11-15 | PMID 28502675
Deng Jiexin, Vozmediano Valvanera, Rodriguez Monica and 2 more
Genes: VKORC1
Mitochondrial ND5 mutation mediated elevated ROS regulates apoptotic pathway epigenetically in a P53 dependent manner for generating pro-cancerous phenotypes.
Mitochondrion | 2017-07-01 | PMID 28502718
Singh Rajnish Kumar, Saini Sunil, Verma Dileep and 2 more
MET Exon 14 Skipping Mutations in Lung Adenocarcinoma: Clinicopathologic Implications and Prognostic Values.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2017-08-01 | PMID 28502721
Lee Geun Dong, Lee Seung Eun, Oh Doo-Yi and 14 more
Genes: MET, ALK, EGFR, KRAS, RET, ROS1
Molecular Diagnosis of Mosaic Overgrowth Syndromes Using a Custom-Designed Next-Generation Sequencing Panel.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502725
Chang Fengqi, Liu Liu, Fang Erica and 5 more
Genes: AKT1
Utility of NIST Whole-Genome Reference Materials for the Technical Validation of a Multigene Next-Generation Sequencing Test.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502726
Shum Bennett O V, Henner Ilya, Belluoccio Daniele and 1 more
Genes: NEO1
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502727
Rasmussen-Torvik Laura J, Almoguera Berta, Doheny Kimberly F and 18 more
Technical Validation of a Next-Generation Sequencing Assay for Detecting Clinically Relevant Levels of Breast Cancer-Related Single-Nucleotide Variants and Copy Number Variants Using Simulated Cell-Free DNA.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502728
Yang Xin, Chu Yuxing, Zhang Rui and 19 more
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502729
Rey Jean-Marc, Ducros Vincent, Pujol Pascal and 5 more
Genes: MUTYH, PMS2, MSH6
Overgrowth Syndromes Caused by Somatic Variants in the Phosphatidylinositol 3-Kinase/AKT/Mammalian Target of Rapamycin Pathway.
The Journal of molecular diagnostics : JMD | 2017-07-01 | PMID 28502730
Akgumus Gozde, Chang Fengqi, Li Marilyn M
Positive family history of aortic dissection dramatically increases dissection risk in family members.
International journal of cardiology | 2017-08-01 | PMID 28502736
Ma Wei-Guo, Chou Alan S, Mok Salvior C M and 7 more
Cytochrome P450 diversity in the tree of life.
Biochimica et biophysica acta. Proteins and proteomics | 2018-01-01 | PMID 28502748
Nelson David R
No association detected between seven common variants in the CDKAL1 gene and gestational glycemic traits.
Molecular and cellular probes | 2017-08-01 | PMID 28502787
Ju Hongfang, Lin Rong, Yuan Ziyu and 4 more
Genes: CDKAL1
Single-Strand Consensus Sequencing Reveals that HIV Type but not Subtype Significantly Impacts Viral Mutation Frequencies and Spectra.
Journal of molecular biology | 2017-07-21 | PMID 28502791
Rawson Jonathan M O, Gohl Daryl M, Landman Sean R and 6 more
Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging.
The Journal of investigative dermatology | 2017-09-01 | PMID 28502801
Law Matthew H, Medland Sarah E, Zhu Gu and 19 more
WDR79/TCAB1 plays a conserved role in the control of locomotion and ameliorates phenotypic defects in SMA models.
Neurobiology of disease | 2017-09-01 | PMID 28502804
Di Giorgio Maria Laura, Esposito Alessandro, Maccallini Paolo and 9 more
Distinct phenotypes of three-repeat and four-repeat human tau in a transgenic model of tauopathy.
Neurobiology of disease | 2017-09-01 | PMID 28502805
Sealey Megan A, Vourkou Ergina, Cowan Catherine M and 5 more
SASP regulation by noncoding RNA.
Mechanisms of ageing and development | 2017-12-01 | PMID 28502821
Panda Amaresh C, Abdelmohsen Kotb, Gorospe Myriam
Ovarian Sertoli-Leydig Cell Tumor with Elevated Inhibin B as a Cause of Secondary Amenorrhea in an Adolescent with Germ Line DICER1 Mutation.
Journal of pediatric and adolescent gynecology | 2017-10-01 | PMID 28502826
Luke Amy M, Moroney John W, Snitchler Andrea and 1 more
Genes: DICER1
With me or against me: Tumor suppressor and drug resistance activities of SAMHD1.
Experimental hematology | 2017-08-01 | PMID 28502830
Herold Nikolas, Rudd Sean G, Sanjiv Kumar and 7 more
Genes: SAMHD1
DNA methylation and DNA methyltransferases.
Epigenetics & chromatin | 2017-01-01 | PMID 28503201
Edwards John R, Yarychkivska Olya, Boulard Mathieu and 1 more
A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote.
BioMed research international | 2017-01-01 | PMID 28503568
Pirastru Monica, Mereu Paolo, Nguyen Chau Quynh and 3 more
Association between NLPR1, NLPR3, and P2X7R Gene Polymorphisms with Partial Seizures.
BioMed research international | 2017-01-01 | PMID 28503575
Wang Haidong, Xu Pengfei, Liao Dehua and 4 more
Genes: NLRP3, NLRP1
Deficiency of Interleukin-1 Receptor Antagonist (DIRA): Report of the First Indian Patient and a Novel Deletion Affecting IL1RN.
Journal of clinical immunology | 2017-07-01 | PMID 28503715
Mendonca Leonardo O, Malle Louise, Donovan Frank X and 10 more
Contribution of germline mutations in cancer predisposition genes to tumor etiology in young women diagnosed with invasive breast cancer.
Breast cancer research and treatment | 2017-08-01 | PMID 28503720
Rummel Seth K, Lovejoy Leann, Shriver Craig D and 1 more
Genes: BRCA2, CHEK2, APC, ATM, BRCA1, CDH1, MUTYH, PALB2
WDR45B-related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome.
Clinical genetics | 2018-02-01 | PMID 28503735
Suleiman J, Allingham-Hawkins D, Hashem M and 3 more
Friends and family: A software program for identification of unrelated individuals from molecular marker data.
Molecular ecology resources | 2017-11-01 | PMID 28503747
de Jager Deon, Swarts Petrus, Harper Cindy and 1 more
The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers.
Clinical genetics | 2018-01-01 | PMID 28503760
Rijken J A, Niemeijer N D, Jonker M A and 14 more
Genes: SDHB
Reducing anti-nutritional factor and enhancing yield with advancing time of planting and zinc application in grasspea in Ethiopia.
Journal of the science of food and agriculture | 2018-01-01 | PMID 28503807
Sarker Ashutosh, Fikre Asnake, El-Moneim Ali M Abd and 2 more
Molecular characterization of equine infectious anaemia virus from a major outbreak in southeastern France.
Transboundary and emerging diseases | 2018-02-01 | PMID 28503813
Gaudaire D, Lecouturier F, Ponçon N and 4 more
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
Clinical genetics | 2018-01-01 | PMID 28503822
Suerink M, Potjer T P, Versluijs A B and 4 more
Genes: PMS2, SPRED1
Demographic histories of three predatory lady beetles reveal complex patterns of diversity and population size change in the United States.
Insect science | 2018-12-01 | PMID 28503842
Sethuraman Arun, Janzen Fredric J, Rubio Michael A and 2 more
TypeLoader: A fast and efficient automated workflow for the annotation and submission of novel full-length HLA alleles.
HLA | 2017-07-01 | PMID 28503844
Surendranath V, Albrecht V, Hayhurst J D and 5 more
Genetic risk score and cardiovascular mortality in a southern european population with coronary artery disease.
International journal of clinical practice | 2017-06-01 | PMID 28503909
Pereira Andreia, Mendonca Maria Isabel, Sousa Ana Célia and 10 more
Genes: CAD
Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.
Human mutation | 2017-08-01 | PMID 28503910
Dou Yanmei, Yang Xiaoxu, Li Ziyi and 10 more
Genes: MAF
New insights into the earliest stages of colorectal tumorigenesis.
Expert review of gastroenterology & hepatology | 2017-08-01 | PMID 28503955
Sievers Chelsie K, Grady William M, Halberg Richard B and 1 more
Essential thrombocythemia: a review of the clinical features, diagnostic challenges, and treatment modalities in the era of molecular discovery.
Leukemia & lymphoma | 2017-12-01 | PMID 28503969
Chuzi Sarah, Stein Brady L
Genes: JAK2, MPL
N-acetylcysteine potentiates diclofenac toxicity in Saccharomyces cerevisiae: stronger potentiation in ABC transporter mutant strains.
Drug and chemical toxicology | 2018-01-01 | PMID 28504001
Al-Attrache Houssein, Chamieh Hala, Hamzé Monzer and 3 more
Different metabolic responses induced by long-term interdisciplinary therapy in obese adolescents related to ACE I/D polymorphism.
Journal of the renin-angiotensin-aldosterone system : JRAAS | 2000-01-01 | PMID 28504003
Almeida Sandro S, Corgosinho Flavia C, Amorim Carlos En and 10 more
Genes: ACE
Detection of driver and subclonal mutations in myelofibrosis: clinical impact on pharmacologic and transplant based treatment strategies.
Expert review of hematology | 2017-07-01 | PMID 28504024
Finazzi Maria Chiara, Lussana Federico, Salmoiraghi Silvia and 2 more
Combination therapy of BRAF inhibitors for advanced melanoma with BRAF V600 mutation: a systematic review and meta-analysis.
The Journal of dermatological treatment | 2018-05-01 | PMID 28504036
Kim Siin, Kim Hyung Tae, Suh Hae Sun
Genes: BRAF
Plasma butyrylcholinesterase activity: a possible biomarker for differential diagnosis between Alzheimer's disease and dementia with Lewy bodies?
The International journal of neuroscience | 2017-12-01 | PMID 28504037
Josviak N D, Batistela M S, Souza R K M and 7 more
Genes: BCHE
Characterization of porcine Trueperella pyogenes by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS), molecular typing and antimicrobial susceptibility profiling in Sao Paulo State.
Comparative immunology, microbiology and infectious diseases | 2017-04-01 | PMID 28504095
Moreno Luisa Z, Matajira Carlos E C, da Costa Barbara L P and 8 more
Multiple clones and low antimicrobial resistance rates for Salmonella enterica serovar Infantis populations in Greece.
Comparative immunology, microbiology and infectious diseases | 2017-04-01 | PMID 28504096
Papadopoulos Theofilos, Petridou Evanthia, Zdragas Antonios and 4 more
Ezrin Ser66 phosphorylation regulates invasion and metastasis of esophageal squamous cell carcinoma cells by mediating filopodia formation.
The international journal of biochemistry & cell biology | 2017-07-01 | PMID 28504189
Li Li-Yan, Xie Ying-Hua, Xie Yang-Min and 9 more
BRAF V600E mutation in pediatric intracranial and cranial juvenile xanthogranuloma.
Human pathology | 2017-11-01 | PMID 28504206
Techavichit Piti, Sosothikul Darintr, Chaichana Thiamjit and 3 more
Genes: BRAF
Antiviral drug resistance and hepatitis B: a continuing public health problem.
Antiviral therapy | 2017-01-01 | PMID 28504241
Littlejohn Margaret
Sirt1 carboxyl-domain is an ATP-repressible domain that is transferrable to other proteins.
Nature communications | 2017-05-15 | PMID 28504272
Kang Hyeog, Oka Shinichi, Lee Duck-Yeon and 13 more
Legionella effector Lpg1137 shuts down ER-mitochondria communication through cleavage of syntaxin 17.
Nature communications | 2017-05-15 | PMID 28504273
Arasaki Kohei, Mikami Yumi, Shames Stephanie R and 3 more
Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases.
Nature communications | 2017-05-15 | PMID 28504275
Wollenberg Valero Katharina C, Garcia-Porta Joan, Rodríguez Ariel and 10 more
Intranuclear and higher-order chromatin organization of the major histone gene cluster in breast cancer.
Journal of cellular physiology | 2018-02-01 | PMID 28504305
Fritz Andrew J, Ghule Prachi N, Boyd Joseph R and 14 more
Genes: CTCF
Rational design of a pH-insensitive cyan fluorescent protein CyPet2 based on the CyPet crystal structure.
FEBS letters | 2017-06-01 | PMID 28504316
Liu Rui, Hu Xiao-Jian, Ding Yu
CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues.
American journal of medical genetics. Part A | 2017-08-01 | PMID 28504353
Luo Minjie, Fan Jinbo, Wenger Tara L and 7 more
Genes: CMIP
Genetic vulnerabilities to prenatal alcohol exposure: Limb defects in sonic hedgehog and GLI2 heterozygous mice.
Birth defects research | 2017-07-03 | PMID 28504423
Fish Eric W, Murdaugh Laura B, Sulik Kathleen K and 2 more
Genes: GLI2
Mycoplasma bovis isolates from dairy calves in Japan have less susceptibility than a reference strain to all approved macrolides associated with a point mutation (G748A) combined with multiple species-specific nucleotide alterations in 23S rRNA.
Microbiology and immunology | 2017-06-01 | PMID 28504455
Sato Toyotaka, Higuchi Hidetoshi, Yokota Shin-Ichi and 1 more
MAP3K1-related gonadal dysgenesis: Six new cases and review of the literature.
American journal of medical genetics. Part C, Seminars in medical genetics | 2017-06-01 | PMID 28504475
Granados Andrea, Alaniz Veronica I, Mohnach Lauren and 6 more
Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.
Archivos argentinos de pediatria | 2017-06-01 | PMID 28504500
Katipoğlu Nagehan, Karapinar Tuba H, Demir Korean and 10 more