Biomedical publications with connected research

Genetic Influence on the Peripheral Blood CD4+ T-cell Differentiation Status in CMV Infection.

The journals of gerontology. Series A, Biological sciences and medical sciences | 2016-12-01 | PMID 26755680

Goldeck David, Larsen Lisbeth Aagaard, Christiansen Lene and 4 more

Plant Morphology of Heterotrimeric G Protein Mutants.

Plant & cell physiology | 2016-03-01 | PMID 26755691

Urano Daisuke, Miura Kotaro, Wu Qingyu and 3 more

Chondrocytic ephrin B2 promotes cartilage destruction by osteoclasts in endochondral ossification.

Development (Cambridge, England) | 2016-02-15 | PMID 26755702

Tonna Stephen, Poulton Ingrid J, Taykar Farzin and 8 more

Genes: ADAMTS4

Phenotypic and genomic analysis of multiple myeloma minimal residual disease tumor cells: a new model to understand chemoresistance.

Blood | 2016-04-14 | PMID 26755711

Paiva Bruno, Corchete Luis A, Vidriales Maria-Belen and 24 more

Genes: ALCAM, CXCR4

Benefit of high-dose daunorubicin in AML induction extends across cytogenetic and molecular groups.

Blood | 2016-03-24 | PMID 26755712

Luskin Marlise R, Lee Ju-Whei, Fernandez Hugo F and 13 more

Genes: NPM1, FLT3

Regulatory Characteristics of Vibrio vulnificus gbpA Gene Encoding a Mucin-binding Protein Essential for Pathogenesis.

The Journal of biological chemistry | 2016-03-11 | PMID 26755724

Jang Kyung Ku, Gil So Yeon, Lim Jong Gyu and 1 more

Genes: CRP

The Quaternary Structure of a Glycoside Hydrolase Dictates Specificity toward β-Glucans.

The Journal of biological chemistry | 2016-03-25 | PMID 26755730

Lafond Mickael, Sulzenbacher Gerlind, Freyd Thibaud and 3 more

Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes.

Human molecular genetics | 2016-03-15 | PMID 26755824

Pers Tune H, Timshel Pascal, Ripke Stephan and 5 more

Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms.

Human molecular genetics | 2016-03-15 | PMID 26755825

Gautam Mukesh, Jara Javier H, Sekerkova Gabriella and 3 more

Genes: UCHL1, ALS2

Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony.

Human molecular genetics | 2016-04-01 | PMID 26755826

Vessoni Alexandre T, Herai Roberto H, Karpiak Jerome V and 6 more

Genes: ERCC6

Exploring the complete mutational space of the LDL receptor LA5 domain using molecular dynamics: linking SNPs with disease phenotypes in familial hypercholesterolemia.

Human molecular genetics | 2016-03-15 | PMID 26755827

Angarica Vladimir Espinosa, Orozco Modesto, Sancho Javier

Overview of hepatitis B virus mutations and their implications in the management of infection.

World journal of gastroenterology | 2016-01-07 | PMID 26755866

Caligiuri Patrizia, Cerruti Rita, Icardi Giancarlo and 1 more

Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect.

The Journal of clinical endocrinology and metabolism | 2016-03-01 | PMID 26756113

Bhatti Tricia R, Ganapathy Karthik, Huppmann Alison R and 9 more

Genes: MEN1

Prediction of Future Osteoporotic Fracture Occurrence by Genetic Profiling: A 6-Year Follow-Up Observational Study.

The Journal of clinical endocrinology and metabolism | 2016-03-01 | PMID 26756118

Lee Seung Hun, Cho Eun-Hee, Ahn Seong Hee and 9 more

Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies.

American journal of medical genetics. Part A | 2016-04-01 | PMID 26756138

Gomez-Ospina Natalia, Bernstein Jonathan A

A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology | 2016-02-01 | PMID 26756145

Miyagawa Maiko, Nishio Shin-Ya, Usami Shin-ichi

The Outlier in All of Us: Why Implementing Pharmacogenomics Could Matter for Everyone.

Clinical pharmacology and therapeutics | 2016-04-01 | PMID 26756170

O'Donnell P H, Danahey K, Ratain M J

Genes: TPMT

Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations.

Diabetic medicine : a journal of the British Diabetic Association | 2016-10-01 | PMID 26756202

Demir T, Onay H, Savage D B and 8 more

Genes: PPARG, LMNA

Computational Trials: Unraveling Motility Phenotypes, Progression Patterns, and Treatment Options for Glioblastoma Multiforme.

PloS one | 2016-01-01 | PMID 26756205

Raman Fabio, Scribner Elizabeth, Saut Olivier and 3 more

Targeted Curing of All Lysogenic Bacteriophage from Streptococcus pyogenes Using a Novel Counter-selection Technique.

PloS one | 2016-01-01 | PMID 26756207

Euler Chad W, Juncosa Barbara, Ryan Patricia A and 3 more

Discovery of 1-{(3R,4R)-3-[({5-Chloro-2-[(1-methyl-1H-pyrazol-4-yl)amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}oxy)methyl]-4-methoxypyrrolidin-1-yl}prop-2-en-1-one (PF-06459988), a Potent, WT Sparing, Irreversible Inhibitor of T790M-Containing EGFR Mutants.

Journal of medicinal chemistry | 2016-03-10 | PMID 26756222

Cheng Hengmiao, Nair Sajiv K, Murray Brion W and 48 more

Genes: EGFR

Circulating Myeloid-Derived Suppressor Cells Predict Differentiated Thyroid Cancer Diagnosis and Extent.

Thyroid : official journal of the American Thyroid Association | 2016-03-01 | PMID 26756227

Angell Trevor E, Lechner Melissa G, Smith Alison M and 5 more

Genetics of psychosis of Alzheimer disease.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2017-01-01 | PMID 26756273

Shah Chintan, DeMichele-Sweet Mary Ann A, Sweet Robert A

Integrated analysis of DNA methylation and mutations in esophageal squamous cell carcinoma.

Molecular carcinogenesis | 2016-12-01 | PMID 26756304

Kishino Takayoshi, Niwa Tohru, Yamashita Satoshi and 7 more

Genes: CHFR, SFRP1, SFRP2, SFRP4, SFRP5, SOX17, WIF1

Longitudinal predictors of cannabis use and dependence in offspring from families at ultra high risk for alcohol dependence and in control families.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2016-04-01 | PMID 26756393

Hill Shirley Y, Jones Bobby L, Steinhauer Stuart R and 2 more

Genes: CNR1, DRD2

Cellular and molecular modifier pathways in tauopathies: the big picture from screening invertebrate models.

Journal of neurochemistry | 2016-04-01 | PMID 26756400

Hannan Shabab B, Dräger Nina M, Rasse Tobias M and 2 more

Genes: MAPT

A founder mutation p.H701P identified as a major cause of SPG7 in Norway.

European journal of neurology | 2016-04-01 | PMID 26756429

Rydning S L, Wedding I M, Koht J and 6 more

Genes: SPG7

Genetic inviability is a major driver of type III survivorship in experimental families of a highly fecund marine bivalve.

Molecular ecology | 2016-02-01 | PMID 26756438

Plough L V, Shin G, Hedgecock D

The impact of CACNA1C allelic variation on regional gray matter volume in Chinese population.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2016-04-01 | PMID 26756527

Huang Liang, Mo Yin, Sun Xuejin and 4 more

Association of PDE4B Polymorphisms with Susceptibility to Schizophrenia: A Meta-Analysis of Case-Control Studies.

PloS one | 2016-01-01 | PMID 26756575

Feng Yanguo, Cheng Dejun, Zhang Chaofeng and 4 more

Insulin-Producing Cells Differentiated from Human Bone Marrow Mesenchymal Stem Cells In Vitro Ameliorate Streptozotocin-Induced Diabetic Hyperglycemia.

PloS one | 2016-01-01 | PMID 26756576

Xin Ying, Jiang Xin, Wang Yishu and 7 more

Generation of Knock-In Pigs Carrying Oct4-tdTomato Reporter through CRISPR/Cas9-Mediated Genome Engineering.

PloS one | 2016-01-01 | PMID 26756580

Lai Sisi, Wei Shu, Zhao Bentian and 12 more

Measuring Selection on Physiology in the Wild and Manipulating Phenotypes (in Terrestrial Nonhuman Vertebrates).

Comprehensive Physiology | 2015-12-15 | PMID 26756627

Husak Jerry F

PD-L1 and Lung Cancer: The Era of Precision-ish Medicine?

Archives of pathology & laboratory medicine | 2016-04-01 | PMID 26756646

Borczuk Alain C, Allen Timothy Craig

The power and promise of RNA-seq in ecology and evolution.

Molecular ecology | 2016-03-01 | PMID 26756714

Todd Erica V, Black Michael A, Gemmell Neil J

Associations between TOMM40 Poly-T Repeat Variants and Dementia in Cases with Parkinsonism.

Journal of Parkinson's disease | 2016-01-01 | PMID 26756745

Lindqvist Daniel, Prokopenko Inga, Londos Elisabet and 2 more

Genes: TOMM40, APOE

Columnar Metaplasia in the Esophageal Remnant After Esophagectomy: A Common Occurrence and a Valuable Insight Into the Development of Barrett Esophagus.

Annals of surgery | 2016-12-01 | PMID 26756755

Dunn Lorna J, Burt Alastair D, Hayes Nicholas and 1 more

Circulating Tumor Cell Phenotype Predicts Recurrence and Survival in Pancreatic Adenocarcinoma.

Annals of surgery | 2016-12-01 | PMID 26756760

Poruk Katherine E, Valero Vicente, Saunders Tyler and 16 more

Associations of TM6SF2 167K allele with liver enzymes and lipid profile in children: the PANIC Study.

Pediatric research | 2016-05-01 | PMID 26756786

Viitasalo Anna, Pihlajamäki Jussi, Paananen Jussi and 3 more

Genetically Divergent Types of the Wheat Leaf Fungus Puccinia triticina in Ethiopia, a Center of Tetraploid Wheat Diversity.

Phytopathology | 2016-04-01 | PMID 26756826

Kolmer J A, Acevedo M A

The Sclerotinia sclerotiorum FoxE2 Gene Is Required for Apothecial Development.

Phytopathology | 2016-05-01 | PMID 26756829

Wang Lu, Liu Yanzhi, Liu Jinliang and 3 more

Absence of Maternal Microchimerism in Regional Lymph Nodes of Children With Biliary Atresia.

Journal of pediatric gastroenterology and nutrition | 2016-06-01 | PMID 26756872

Engelmann Carsten, Maelzer Madeleine, Kreyenberg Hermann

A Follow-Up of the Multicenter Collaborative Study on HIV-1 Drug Resistance and Tropism Testing Using 454 Ultra Deep Pyrosequencing.

PloS one | 2016-01-01 | PMID 26756901

St John Elizabeth P, Simen Birgitte B, Turenchalk Gregory S and 16 more

Factors Associated With Rates of False-Positive and False-Negative Results From Digital Mammography Screening: An Analysis of Registry Data.

Annals of internal medicine | 2016-02-16 | PMID 26756902

Nelson Heidi D, O'Meara Ellen S, Kerlikowske Karla and 2 more

Disrupted in schizophrenia 1 (DISC1) L100P mutants have impaired activity-dependent plasticity in vivo and in vitro.

Translational psychiatry | 2016-01-12 | PMID 26756905

Tropea D, Molinos I, Petit E and 9 more

Genes: DISC1

Research Progresses in Understanding the Pathophysiology of Moyamoya Disease.

Cerebrovascular diseases (Basel, Switzerland) | 2016-01-01 | PMID 26756907

Bersano Anna, Guey Stephanie, Bedini Gloria and 22 more

Genes: MMD

Direct sequencing and analysis of the genomes of newly emerging GII.17 norovirus strains in South China.

Journal of applied microbiology | 2016-04-01 | PMID 26756909

Xue L, Cai W, Wu Q and 2 more

Genes: IMPACT

Identification of recombination in the NS1 and VPs genes of parvovirus B19.

Journal of medical virology | 2016-08-01 | PMID 26756922

Shen Hongxing, Zhang Wen, Wang Hua and 1 more

Treatment to sustain a Th17-type phenotype to prevent skewing toward Treg and to limit premalignant lesion progression to cancer.

International journal of cancer | 2016-05-15 | PMID 26756968

Young M Rita I, Levingston Corinne A, Johnson Sara D

Climate structures genetic variation across a species' elevation range: a test of range limits hypotheses.

Molecular ecology | 2016-02-01 | PMID 26756973

Sexton Jason P, Hufford Matthew B, Bateman Ashley C and 4 more

Chronic Sleep Deprivation Exacerbates Learning-Memory Disability and Alzheimer's Disease-Like Pathologies in AβPP(swe)/PS1(ΔE9) Mice.

Journal of Alzheimer's disease : JAD | 2016-01-01 | PMID 26757041

Qiu Hongyan, Zhong Rujia, Liu Hui and 3 more

Genetic and Nongenetic Factors Affecting Clopidogrel Response in the Egyptian Population.

Clinical and translational science | 2016-02-01 | PMID 26757134

Khalil B M, Shahin M H, Solayman M H M and 8 more

Genes: ABCB1, CES1

Natural history collections as windows on evolutionary processes.

Molecular ecology | 2016-02-01 | PMID 26757135

Holmes Michael W, Hammond Talisin T, Wogan Guinevere O U and 8 more

Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic test.

Clinical genetics | 2016-06-01 | PMID 26757139

Thevenon J, Duffourd Y, Masurel-Paulet A and 12 more

Lower Prevalence of Alzheimer's Disease among Tibetans: Association with Religious and Genetic Factors.

Journal of Alzheimer's disease : JAD | 2016-01-01 | PMID 26757186

Huang Fukai, Shang Ying, Luo Yuandai and 6 more

Genes: CLU, BIN1, TFAM

Association of Butyrylcholinesterase-K Allele and Apolipoprotein E ɛ4 Allele with Cognitive Decline in Dementia with Lewy Bodies and Alzheimer's Disease.

Journal of Alzheimer's disease : JAD | 2016-01-01 | PMID 26757188

Vijayaraghavan Swetha, Darreh-Shori Taher, Rongve Arvid and 8 more

Genes: BCHE

Familial Presenilin Mutations and Sporadic Alzheimer's Disease Pathology: Is the Assumption of Biochemical Equivalence Justified?

Journal of Alzheimer's disease : JAD | 2016-01-01 | PMID 26757189

Roher Alex E, Maarouf Chera L, Kokjohn Tyler A

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

Journal of Alzheimer's disease : JAD | 2016-01-01 | PMID 26757195

Oldoni Emanuela, Fumagalli Giorgio G, Serpente Maria and 25 more

Genes: PRNP

On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set.

Annals of human genetics | 2016-03-01 | PMID 26757198

Wu Baolin, Guan Weihua, Pankow James S

How mutational epistasis impairs predictability in protein evolution and design.

Protein science : a publication of the Protein Society | 2016-07-01 | PMID 26757214

Miton Charlotte M, Tokuriki Nobuhiko

A Mutant of the Bck1 Homolog from Cryphonectria parasitica Resulted in Sectorization with an Impaired Pathogenicity.

Molecular plant-microbe interactions : MPMI | 2016-04-01 | PMID 26757242

Kim Jung-Mi, Lee Joong-Gi, Yun Suk-Hyun and 5 more

Identification of Quantitative Trait Loci for the Phenolic Acid Contents and Their Association with Agronomic Traits in Tibetan Wild Barley.

Journal of agricultural and food chemistry | 2016-02-03 | PMID 26757245

Cai Shengguan, Han Zhigang, Huang Yuqing and 3 more

The evolution of highly variable immunity genes across a passerine bird radiation.

Molecular ecology | 2016-02-01 | PMID 26757248

O'Connor E A, Strandh M, Hasselquist D and 2 more

Genetic variants in ABCG1 are associated with survival of nonsmall-cell lung cancer patients.

International journal of cancer | 2016-06-01 | PMID 26757251

Wang Yanru, Liu Hongliang, Ready Neal E and 4 more

Genes: ABCG1

DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation.

Clinical genetics | 2016-06-01 | PMID 26757254

Urquhart J E, Beaman G, Byers H and 12 more

Genes: DMRTA2

Intravenous administration of brain-targeted stable nucleic acid lipid particles alleviates Machado-Joseph disease neurological phenotype.

Biomaterials | 2016-03-01 | PMID 26757259

Conceição Mariana, Mendonça Liliana, Nóbrega Clévio and 7 more

Gene-environment interaction and risk of breast cancer.

British journal of cancer | 2016-01-19 | PMID 26757262

Rudolph Anja, Chang-Claude Jenny, Schmidt Marjanka K

The association of Asn453Ser polymorphism in CYP1B1 gene with selected somatic and biochemical variables in Slovak women of different menopause status.

Menopause (New York, N.Y.) | 2016-05-01 | PMID 26757271

Čerňanová Veronika, Danková Zuzana, Luptáková Lenka and 2 more

Pharmacogenetics and Treatment Response in Narcolepsy Type 1: Relevance of the Polymorphisms of the Drug Transporter Gene ABCB1.

Clinical neuropharmacology | 2000-01-01 | PMID 26757307

Moresco Monica, Riccardi Laura Natalia, Pizza Fabio and 4 more

Genes: ABCB1

Cystatin C as a p53-inducible apoptotic mediator that regulates cathepsin L activity.

Cancer science | 2016-03-01 | PMID 26757339

Mori Jinichi, Tanikawa Chizu, Funauchi Yuki and 3 more

Current Understanding of the Genetic Architecture of Rhegmatogenous Retinal Detachment.

Ophthalmic genetics | 2016-06-01 | PMID 26757352

Johnston Timothy, Chandra Aman, Hewitt Alex W

The MTHFR C677T Polymorphism and Risk of Intracerebral Hemorrhage in a Chinese Han Population.

Medical science monitor : international medical journal of experimental and clinical research | 2016-01-12 | PMID 26757363

Hu Xin, Tao Chuanyuan, Xie Zhiyi and 6 more

Genes: MTHFR

Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing.

Clinical genetics | 2016-10-01 | PMID 26757417

Ng P S, Wen W X, Fadlullah M Z H and 6 more

Genes: BRCA2, BRCA1, BARD1, PALB2

Placental Microparticles and MicroRNAs in Pregnant Women with Plasmodium falciparum or HIV Infection.

PloS one | 2016-01-01 | PMID 26757431

Moro Laura, Bardají Azucena, Macete Eusebio and 11 more

The relationship between EMT, CD44high /EGFRlow phenotype, and treatment response in head and neck cancer cell lines.

Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology | 2016-10-01 | PMID 26757432

Johansson Ann-Charlotte, La Fleur Linnea, Melissaridou Styliani and 1 more

Genes: EGFR, TWIST1, CDH1, CDH2, FOXC2, VIM

A novel sweet potato potyvirus open reading frame (ORF) is expressed via polymerase slippage and suppresses RNA silencing.

Molecular plant pathology | 2016-09-01 | PMID 26757490

Untiveros Milton, Olspert Allan, Artola Katrin and 3 more

[Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa].

La Tunisie medicale | 2015-07-01 | PMID 26757501

Chouchene Ibtissem, Largueche Leila, Derouiche Kaouther and 3 more

Genes: RPE65

[The JAK2 mutation in myeloproliferative disorders: A predictive factor of thrombosis].

La Tunisie medicale | 2015-07-01 | PMID 26757507

Mahjoub Sonia, Baccouche Héla, Sahnoun Mariam and 4 more

Genes: JAK2, BCR

Hepatitis C Virus in Children: Deferring Treatment in Expectation of Direct-Acting Antiviral Agents.

The Israel Medical Association journal : IMAJ | 2015-11-01 | PMID 26757569

Granot Esther, Sokal Etienne M

Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis.

Journal of clinical research in pediatric endocrinology | 2016-06-05 | PMID 26757598

Bao Shan, Cai Jun Hong, Yang Shu Ying and 4 more

Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis.

Journal of clinical research in pediatric endocrinology | 2016-03-05 | PMID 26757609

Liu Shiguo, Chai Jian, Zheng Guohua and 3 more

Genes: HHEX

Evaluation of genotoxic and antigenotoxic effects of boron by the somatic mutation and recombination test (SMART) on Drosophila.

Drug and chemical toxicology | 2016-10-01 | PMID 26757614

Sarıkaya Rabia, Erciyas Kamile, Kara Muhammed Isa and 3 more

Genomic characterization of primary central nervous system lymphoma.

Acta neuropathologica | 2016-06-01 | PMID 26757737

Fukumura Kazutaka, Kawazu Masahito, Kojima Shinya and 19 more

Genes: MYD88, BTG2, GRB2, PIM1

Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).

Hemoglobin | 2016-01-01 | PMID 26757782

He Yi, Zhao Ying, Lou Ji-Wu and 2 more

Genes: HBA2

Association of ACTN3 R577X but not ACE I/D gene variants with elite rugby union player status and playing position.

Physiological genomics | 2016-03-01 | PMID 26757799

Heffernan S M, Kilduff L P, Erskine R M and 16 more

Genes: ACTN3, ACE

Vitamin D status predicts reproductive fitness in a wild sheep population.

Scientific reports | 2016-01-13 | PMID 26757805

Handel Ian, Watt Kathryn A, Pilkington Jill G and 8 more

Efficient transgenesis mediated by pigmentation rescue in zebrafish.

BioTechniques | 2016-01-01 | PMID 26757807

Harrold Itrat, Carbonneau Seth, Moore Bethany M and 6 more

Development of single-tube nested real-time PCR assays with long internally quenched probes for detection of norovirus genogroup II.

BioTechniques | 2016-01-01 | PMID 26757809

Xia Hongyan, Gravelsina Sabine, Öhrmalm Christina and 2 more

Molecular markers for tolerance of European ash (Fraxinus excelsior) to dieback disease identified using Associative Transcriptomics.

Scientific reports | 2016-01-13 | PMID 26757823

Harper Andrea L, McKinney Lea Vig, Nielsen Lene Rostgaard and 12 more

RNA recombination in Hepatitis delta virus: Identification of a novel naturally occurring recombinant.

Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi | 2017-12-01 | PMID 26757847

Lin Chia-Chi, Lee Chi-Ching, Lin Siao-Han and 5 more

[Effect of VKORC1 and CYP2C9 variants on dosage of oral anticoagulants in Chilean individuals].

Revista medica de Chile | 2015-11-01 | PMID 26757860

Benavides Felipe, Grossman Nicole, Poggi Helena and 10 more

Genes: VKORC1

[Association between genotype and allele frequencies of CYP2A6*12 and rs16969968 in CHRNA5 variants with smoking and body mass index in young subjects from Northeast Mexico].

Revista medica de Chile | 2015-11-01 | PMID 26757861

Borrego-Soto Gissela, Costilla-Esquivel Antonio, Padilla-Rivas Gerardo Raymundo and 6 more

Genes: CHRNA5

Farewell to GBM-O: Genomic and transcriptomic profiling of glioblastoma with oligodendroglioma component reveals distinct molecular subgroups.

Acta neuropathologica communications | 2016-01-13 | PMID 26757882

Hinrichs Benjamin H, Newman Scott, Appin Christina L and 6 more

Genes: IDH1, EGFR, PDGFRA

Prognostic Genetic Signatures in Upper Tract Urothelial Carcinoma.

Current urology reports | 2016-02-01 | PMID 26757906

Li Qiang, Bagrodia Aditya, Cha Eugene K and 1 more

[Clinical characteristics, prognosis and genetic susceptibility of herpes simplex encephalitis in children].

Zhonghua er ke za zhi = Chinese journal of pediatrics | 2015-09-01 | PMID 26757972

Feng Wenya, Chen Tianming, Hu Bing and 2 more

Genes: TLR3

Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia.

European journal of human genetics : EJHG | 2016-08-01 | PMID 26757980

Cavé Hélène, Caye Aurélie, Ghedira Nehla and 30 more

Genes: RIT1, PTPN11

De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila.

European journal of human genetics : EJHG | 2016-08-01 | PMID 26757981

Lugtenberg Dorien, Reijnders Margot R F, Fenckova Michaela and 27 more

Genes: WAC

Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.

European journal of human genetics : EJHG | 2016-08-01 | PMID 26757982

Kan Mengyuan, Auer Paul L, Wang Gao T and 34 more

Genes: IKBKB

Nitrogen Use Efficiency Is Mediated by Vacuolar Nitrate Sequestration Capacity in Roots of Brassica napus.

Plant physiology | 2016-03-01 | PMID 26757990

Han Yong-Liang, Song Hai-Xing, Liao Qiong and 10 more

Using global transcription machinery engineering (gTME) to improve ethanol tolerance of Zymomonas mobilis.

Microbial cell factories | 2016-01-13 | PMID 26758018

Tan Furong, Wu Bo, Dai Lichun and 6 more