Biomedical publications with connected research

High-resolution association mapping with libraries of immortalized lines from ancestral landraces.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2022-01-01 | PMID 34668978

Würschum Tobias, Weiß Thea M, Renner Juliane and 9 more

Stereotactic body radiotherapy to the primary lung lesion improves the survival of the selected patients with non-oligometastatic NSCLC harboring EGFR activating mutation with first-line EGFR-TKIs: a real-world study.

Journal of cancer research and clinical oncology | 2022-10-01 | PMID 34669037

Wei Hao, Zhou Xiaojuan, Yang Hui and 12 more

Risk of migraine contributed by genetic polymorphisms of ANKDD1B gene: a case-control study based on Chinese Han population.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022-04-01 | PMID 34669083

Zhang Tianxiao, Wei Hang, Li Miao and 6 more

Identification of women at risk of hereditary breast-ovarian cancer among participants in a population-based breast cancer screening.

Familial cancer | 2022-07-01 | PMID 34669096

Bonelli Luigina, Valle Ivana, Rebora Ivana and 6 more

A review on interplay between obesity, lipoprotein profile and nutrigenetics with selected candidate marker genes of type 2 diabetes mellitus.

Molecular biology reports | 2022-01-01 | PMID 34669123

Bhori Mustansir, Rastogi Varuni, Tungare Kanchanlata and 1 more

Mitochondrial DNA sequence variation and risk of meningioma.

Journal of neuro-oncology | 2021-12-01 | PMID 34669147

Samanic Claudine M, Teer Jamie K, Thompson Zachary J and 6 more

Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation - High-Grade PitNET or PitNEC?

Endocrine pathology | 2022-06-01 | PMID 34669159

Saeger Wolfgang, Mawrin Christian, Meinhardt Matthias and 2 more

Creating Cell Model 2.0 Using Patient Samples Carrying a Pathogenic Mitochondrial DNA Mutation: iPSC Approach for LHON.

Methods in molecular biology (Clifton, N.J.) | 2022-01-01 | PMID 34669166

Singh Pragya, Bahr Tyler, Zhao Xiaoxu and 4 more

Phenotypic plasticity drives phenological changes in a Mediterranean blue tit population.

Journal of evolutionary biology | 2022-02-01 | PMID 34669221

Biquet Juliette, Bonamour Suzanne, de Villemereuil Pierre and 2 more

Immune characterization of a Colombian family cluster with SARS-CoV-2 infection.

Biomedica : revista del Instituto Nacional de Salud | 2021-10-15 | PMID 34669281

Aguilar-Jiménez Wbeimar, Flórez-Álvarez Lizdany, Rincón Daniel S and 13 more

[Association of polymorphic markers rs7947461 of the TRIM21 gene and rs33996649 of the PTPN22 gene with the risk of developing exogenous dry eye syndrome].

Vestnik oftalmologii | 2021-01-01 | PMID 34669330

Safonova T N, Zaitseva G V, Burdennyy A M and 1 more

[New possibilities in diagnosis of hereditary optic neuropathies].

Vestnik oftalmologii | 2021-01-01 | PMID 34669349

Sheremet N L, Krylova T D, Tsygankova P G

[Clinical and genetic aspects of ABCA4-associated inherited retinal diseases].

Vestnik oftalmologii | 2021-01-01 | PMID 34669350

Sheremet N L, Strelnikov V V

Germline Testing in Prostate Cancer: When and Who to Test.

Oncology (Williston Park, N.Y.) | 2021-10-20 | PMID 34669358

Sokolova Alexandra, Cheng Heather

Functional Genomic Analyses Reveal an Open Pan-genome for the Chloroviruses and a Potential for Genetic Innovation in New Isolates.

Journal of virology | 2022-01-26 | PMID 34669449

Rodrigues Rodrigo A L, Queiroz Victória F, Ghosh Jayadri and 2 more

Obese, non-eosinophilic asthma: frequent exacerbators in a real-world setting.

The Journal of asthma : official journal of the Association for the Care of Asthma | 2022-11-01 | PMID 34669527

Ananth Sachin, Navarra Alessio, Vancheeswaran Rama

Asthma Phenotypes and COVID-19 Risk: A Population-based Observational Study.

American journal of respiratory and critical care medicine | 2022-01-01 | PMID 34669568

Bloom Chloe I, Cullinan Paul, Wedzicha Jadwiga A

Correlation of circulating tumor DNA EGFR mutation levels with clinical outcomes in patients with advanced lung adenocarcinoma.

Chinese medical journal | 2021-09-30 | PMID 34669636

Liu Xiang-Liang, Bai Ri-Lan, Chen Xiao and 10 more

Induced pluripotent stem cell-derived motor neurons from amyotrophic lateral sclerosis (ALS) patients carrying different superoxide dismutase 1 mutations recapitulate pathological features of ALS.

Chinese medical journal | 2021-10-06 | PMID 34669638

Liu Wen-Chao, Liu Na, Wang Yan and 5 more

Resistance mechanisms to osimertinib and emerging therapeutic strategies in nonsmall cell lung cancer.

Current opinion in oncology | 2022-01-01 | PMID 34669648

Zeng Yue, Yu Danlei, Tian Wentao and 1 more

Molecular genotyping of adrenocortical carcinoma: a systematic analysis of published literature 2019-2021.

Current opinion in oncology | 2022-01-01 | PMID 34669649

Grisanti Salvatore, Cosentini Deborah, Sigala Sandra and 1 more

Prolidase Deficiency Causing Recalcitrant Leg Ulcerations in Siblings.

Advances in skin & wound care | 2021-11-01 | PMID 34669667

Hajjar Nancy, Kabbani Mariam, Tannous Rim and 4 more

Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis.

PloS one | 2021-01-01 | PMID 34669720

Charfeddine Cherine, Laroussi Nadia, Mkaouar Rahma and 10 more

Rapid resistance development to three antistaphylococcal therapies in antibiotic-tolerant staphylococcus aureus bacteremia.

PloS one | 2021-01-01 | PMID 34669727

Miller Christopher R, Monk Jonathan M, Szubin Richard and 1 more

Leveraging auxiliary data from arbitrary distributions to boost GWAS discovery with Flexible cFDR.

PLoS genetics | 2021-10-01 | PMID 34669738

Hutchinson Anna, Reales Guillermo, Willis Thomas and 1 more

Mutation resource of Samba Mahsuri revealed the presence of high extent of variations among key traits for rice improvement.

PloS one | 2021-01-01 | PMID 34669755

Potupureddi Gopi, Balija Vishalakshi, Ballichatla Suneel and 20 more

Comparative metavirome analysis in polytransfused patients.

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas | 2021-01-01 | PMID 34669783

Valença I N, Rós F A, Zucherato V S and 4 more

Morphometric measurements and carcass characteristics of Black Australorp, Naked Neck, and Rhode Island Red crossbreds under alternative production systems.

Brazilian journal of biology = Revista brasleira de biologia | 2021-01-01 | PMID 34669811

Usman M, Ishaq H M, Mahmud A and 8 more

rs7903146 mutation of Type 2 diabetes mellitus-related gene TCF7L2 is not associated with polycystic ovary syndrome in a cohort of Turkey.

Revista da Associacao Medica Brasileira (1992) | 2021-08-01 | PMID 34669858

Taşkin Emre, Eroğlu Semra

The Thyroid Hormone Transporter MCT10 Is a Novel Regulator of Trabecular Bone Mass and Bone Turnover in Male Mice.

Endocrinology | 2022-01-01 | PMID 34669927

Lademann Franziska, Mayerl Steffen, Tsourdi Elena and 7 more

Genetically Predicted Lifelong Circulating 25(OH)D Levels are Associated With Serum Calcium Levels and Kidney Stone Risk.

The Journal of clinical endocrinology and metabolism | 2022-02-17 | PMID 34669929

Jian Zhongyu, Huang Yu, He Yazhou and 4 more

Identification of Enzymes from Pseudogluconobacter saccharoketogenes Producing d-Glucaric Acid from d-Glucose.

Bioscience, biotechnology, and biochemistry | 2021-12-22 | PMID 34669931

Ito Tetsuya, Masaki Hisaharu, Fujita Koki and 4 more

Interaction between rs10830962 polymorphism in MTNR1B and lifestyle intervention on maternal and neonatal outcomes: secondary analyses of the DALI lifestyle randomized controlled trial.

The American journal of clinical nutrition | 2022-02-09 | PMID 34669935

van Poppel Mireille N M, Corcoy Rosa, Hill David and 5 more

Causes and Consequences of Polycystic Ovary Syndrome: Insights From Mendelian Randomization.

The Journal of clinical endocrinology and metabolism | 2022-02-17 | PMID 34669940

Zhu Tiantian, Goodarzi Mark O

webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.

Nucleic acids research | 2022-01-07 | PMID 34669946

Cao Chen, Wang Jianhua, Kwok Devin and 5 more

Deep learning predicts epidermal growth factor receptor mutation subtypes in lung adenocarcinoma.

Medical physics | 2021-12-01 | PMID 34669994

Song Jiangdian, Ding Changwei, Huang Qinlai and 4 more

AQP1 Promoter Variant, Water Transport, and Outcomes in Peritoneal Dialysis.

The New England journal of medicine | 2021-10-21 | PMID 34670044

Morelle Johann, Marechal Céline, Yu Zanzhe and 21 more

Identification and structure characterization of novel IDS variants causing mucopolysaccharidosis type II: A retrospective analysis of 30 Chinese children.

Clinica chimica acta; international journal of clinical chemistry | 2021-12-01 | PMID 34670126

Zhao Xiao-Ying, Qiao Guang-Ming, Liu Fang

Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis.

Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia | 2021-09-01 | PMID 34670306

Coelho Maria Liz, Soares Elisa, Freixo Marília and 4 more

[Hereditary kidney cancer - easily clarified and diagnosed with ToSCaNA].

Aktuelle Urologie | 2022-09-01 | PMID 34670316

Fuhrmann Christian, Czerner Christoph P, Ripperger Tim and 1 more

Novel ceruloplasmin gene mutation causing aceruloplasminemia with diabetes in a Chinese woman: a case report.

Annals of palliative medicine | 2022-07-01 | PMID 34670377

Xiao Yuanyuan, Zhu Chaoyu, Jiang Fusong and 4 more

Cost-effectiveness analysis of glecaprevir/pibrentasvir regimen for treating Chinese patients with chronic hepatitis C genotype 1 and genotype 2 infection.

Annals of palliative medicine | 2021-10-01 | PMID 34670381

Zhou Hui-Jun, Wu Gang, Li Ji-Ming and 5 more

Genotype-Guided P2Y12 Inhibitor Therapy After Percutaneous Coronary Intervention: A Bayesian Analysis.

Circulation. Genomic and precision medicine | 2021-12-01 | PMID 34670396

Parcha Vibhu, Heindl Brittain F, Li Peng and 5 more

Endothelial GNAQ p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels.

Arteriosclerosis, thrombosis, and vascular biology | 2022-01-01 | PMID 34670408

Huang Lan, Bichsel Colette, Norris Alexis L and 9 more

Genes: ANGPT2, GNAQ

Molecular signatures of Janthinobacterium lividum from Trinidad support high potential for crude oil metabolism.

BMC microbiology | 2021-10-20 | PMID 34670489

Ramdass Amanda C, Rampersad Sephra N

DEL in China: the D antigen among serologic RhD-negative individuals.

Journal of translational medicine | 2021-10-20 | PMID 34670559

Yin Qinan, Flegel Willy Albert

Prevalence, characteristics, and distribution of HPV genotypes in women from Zhejiang Province, 2016-2020.

Virology journal | 2021-10-20 | PMID 34670576

Yan Xiaotian, Shen Lingwei, Xiao Yufei and 3 more

Gut-microbiota-microglia-brain interactions in Alzheimer's disease: knowledge-based, multi-dimensional characterization.

Alzheimer's research & therapy | 2021-10-20 | PMID 34670619

Wang QuanQiu, Davis Pamela B, Qi Xin and 5 more

Lung cancer is also a hereditary disease.

European respiratory review : an official journal of the European Respiratory Society | 2021-12-31 | PMID 34670806

Benusiglio Patrick R, Fallet Vincent, Sanchis-Borja Mateo and 2 more

A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin.

Internal medicine (Tokyo, Japan) | 2022-05-15 | PMID 34670883

Sano Yasuteru, Ota Satoko, Oishi Mariko and 6 more

A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed Carbamoyl Phosphate Synthase 1 Gene Monoallelic Mutation.

Internal medicine (Tokyo, Japan) | 2022-05-01 | PMID 34670888

Ishikawa Ruoyi, Sugimoto Takamichi, Abe Takafumi and 9 more

Combined Mutation of the GATA2 Gene and STAT5B Gene in a Patient with Hypogammaglobulinemia and Autoimmunity.

The Tohoku journal of experimental medicine | 2021-10-01 | PMID 34670919

Liu Zhihui, Qing Pingying, Zhao Yi and 2 more

Phenotyping in acute respiratory distress syndrome: state of the art and clinical implications.

Current opinion in critical care | 2022-02-01 | PMID 34670998

Alipanah Narges, Calfee Carolyn S

Viral genome wide association study identifies novel hepatitis C virus polymorphisms associated with sofosbuvir treatment failure.

Nature communications | 2021-10-20 | PMID 34671027

Smith David A, Fernandez-Antunez Carlota, Magri Andrea and 12 more

Population structure, biogeography and transmissibility of Mycobacterium tuberculosis.

Nature communications | 2021-10-20 | PMID 34671035

Freschi Luca, Vargas Roger, Husain Ashaque and 10 more

Structural and functional analysis of target recognition by the lymphocyte adaptor protein LNK.

Nature communications | 2021-10-20 | PMID 34671038

Morris Rhiannon, Zhang Yaoyuan, Ellyard Julia I and 5 more

Molecular insights into receptor binding of recent emerging SARS-CoV-2 variants.

Nature communications | 2021-10-20 | PMID 34671049

Han Pengcheng, Su Chao, Zhang Yanfang and 21 more

Prognostic significance of FLT3-ITD length in AML patients treated with intensive regimens.

Scientific reports | 2021-10-20 | PMID 34671057

Castaño-Bonilla Tamara, Alonso-Dominguez Juan M, Barragán Eva and 33 more

Ancient DNA SNP-panel data suggests stability in bluefin tuna genetic diversity despite centuries of fluctuating catches in the eastern Atlantic and Mediterranean.

Scientific reports | 2021-10-20 | PMID 34671077

Andrews Adam J, Puncher Gregory N, Bernal-Casasola Darío and 14 more

Genetic landscape of T cells identifies synthetic lethality for T-ALL.

Communications biology | 2021-10-20 | PMID 34671088

O'Meara Connor P, Guerri Lucia, Lawir Divine-Fondzenyuy and 10 more

Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer.

Journal of human genetics | 2022-03-01 | PMID 34671089

Hikino Keiko, Koido Masaru, Otomo Nao and 6 more

Nine-gene pharmacogenomics profile service: The Mayo Clinic experience.

The pharmacogenomics journal | 2022-02-01 | PMID 34671112

Matey Eric T, Ragan Ashley Kate, Oyen Lance J and 12 more

Distinct clinico-biological features in AML patients with low allelic ratio FLT3-ITD: role of allogeneic stem cell transplantation in first remission.

Bone marrow transplantation | 2022-01-01 | PMID 34671120

Tien Feng-Ming, Tsai Xavier Cheng-Hong, Huang Sheng-Chuan and 20 more

Genes: FLT3, CR1, AR, EFS

Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/β-catenin-Cyp2e1 Signaling.

International journal of biological sciences | 2021-01-01 | PMID 34671210

Chen Li-Jie, Lin Xiu-Xian, Guo Jing and 13 more

Association of Estrogen Receptor Genes Polymorphisms With Polycystic Ovary Syndrome: A Systematic Review and Meta-Analysis Based on Observational Studies.

Frontiers in endocrinology | 2021-01-01 | PMID 34671317

Zhou Siyu, Wen Shu, Sheng Yongcheng and 5 more

Complement Factor H Family Proteins Modulate Monocyte and Neutrophil Granulocyte Functions.

Frontiers in immunology | 2021-01-01 | PMID 34671340

Kárpáti Éva, Kremlitzka Mariann, Sándor Noémi and 3 more

CGAT: Cell Graph ATtention Network for Grading of Pancreatic Disease Histology Images.

Frontiers in immunology | 2021-01-01 | PMID 34671349

Baranwal Mayank, Krishnan Santhoshi, Oneka Morgan and 2 more

Computational Inference, Validation, and Analysis of 5'UTR-Leader Sequences of Alleles of Immunoglobulin Heavy Chain Variable Genes.

Frontiers in immunology | 2021-01-01 | PMID 34671351

Huang Yixun, Thörnqvist Linnea, Ohlin Mats

The Association Between Single-Nucleotide Polymorphisms of Co-Stimulatory Genes Within Non-HLA Region and the Prognosis of Leukemia Patients With Hematopoietic Stem Cell Transplantation.

Frontiers in immunology | 2021-01-01 | PMID 34671352

Chen Ding-Ping, Chang Su-Wei, Wang Po-Nan and 4 more

Automatic Film Label Acquisition Method Based on Improved Neural Networks Optimized by Mutation Ant Colony Algorithm.

Computational intelligence and neuroscience | 2021-01-01 | PMID 34671392

Liu Junjie

Predicting Cross-Species Infection of Swine Influenza Virus with Representation Learning of Amino Acid Features.

Computational and mathematical methods in medicine | 2021-01-01 | PMID 34671417

Kou Zheng, Li Junjie, Fan Xinyue and 2 more

Longitudinal Effects of Physical Activity Change on Hippocampal Volumes over up to 12 Years in Middle and Older Age Community-Dwelling Individuals.

Cerebral cortex (New York, N.Y. : 1991) | 2022-06-16 | PMID 34671805

Fraser Mark A, Walsh Erin I, Shaw Marnie E and 2 more

Detection of in-frame mutation by IS30-family insertion sequence in the phospholipid phosphatidylglycerol synthase gene (pgsA2) of high-level daptomycin-resistant Corynebacterium striatum.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2022-02-01 | PMID 34671843

Gotoh Kazuyoshi, Mayura I Putu Bayu, Enomoto Yusaku and 4 more

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7.

Journal of clinical immunology | 2022-01-01 | PMID 34671876

Caseley Emily A, Lara-Reyna Samuel, Poulter James A and 6 more

Starch synthases SSIIa and GBSSI control starch structure but do not determine starch granule morphology in the absence of SSIIIa and SSIVb.

Plant molecular biology | 2022-03-01 | PMID 34671919

Crofts Naoko, Domon Asaka, Miura Satoko and 5 more

The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.

Clinical genetics | 2022-02-01 | PMID 34671974

Stevens Servi J C, Stumpel Constance T R M, Diderich Karin E M and 12 more

Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China.

Clinical genetics | 2022-01-01 | PMID 34671977

Yang Lin, Wei Zejun, Chen Xiang and 24 more

Experiential modulation of social dominance in a SYNGAP1 rat model of Autism Spectrum Disorders.

The European journal of neuroscience | 2021-11-01 | PMID 34672048

Harris Emma, Myers Honor, Saxena Kapil and 4 more

Heritable variation in locomotion, reward sensitivity and impulsive behaviors in a genetically diverse inbred mouse panel.

Genes, brain, and behavior | 2021-11-01 | PMID 34672075

Bailey Lauren S, Bagley Jared R, Dodd Rainy and 9 more

Risk-Reducing Salpingo-Oophorectomy and the Use of Hormone Replacement Therapy Below the Age of Natural Menopause: Scientific Impact Paper No. 66 October 2021: Scientific Impact Paper No. 66.

BJOG : an international journal of obstetrics and gynaecology | 2022-01-01 | PMID 34672090

Manchanda R, Gaba F, Talaulikar V and 4 more

Detection of the HLA-A*11:32:01 allele in a Taiwanese bone marrow donor.

HLA | 2022-02-01 | PMID 34672119

Yang Kuo-Liang, Li Chi-Cheng, Lin Py-Yu

Cost-utility analysis of single nucleotide polymorphism panel-based machine learning algorithm to predict risk of opioid use disorder.

Journal of comparative effectiveness research | 2021-12-01 | PMID 34672212

Mallow Peter J, Belk Kathy W

The efficacy of immunohistochemistry in the diagnosis of molecular genetic alterations in central nervous system gliomas: Next-generation sequencing of 212 mutations in 112 patients.

Clinical neuropathology | 2000-01-01 | PMID 34672256

Daoud Elena V, Chkheidze Rati, Yell Paul C and 3 more

Utilizing preclinical models of genetic diversity to improve translation of phytochemical activities from rodents to humans and inform personalized nutrition.

Food & function | 2021-11-15 | PMID 34672309

Iglesias-Carres Lisard, Neilson Andrew P

HPODNets: deep graph convolutional networks for predicting human protein-phenotype associations.

Bioinformatics (Oxford, England) | 2022-01-12 | PMID 34672333

Liu Lizhi, Mamitsuka Hiroshi, Zhu Shanfeng

Optimizing viral genome subsampling by genetic diversity and temporal distribution (TARDiS) for phylogenetics.

Bioinformatics (Oxford, England) | 2022-01-12 | PMID 34672334

Marini Simone, Mavian Carla, Riva Alberto and 3 more

Nucleotide Substitutions during Speciation may Explain Substitution Rate Variation.

Systematic biology | 2022-08-10 | PMID 34672354

Janzen Thijs, Bokma Folmer, Etienne Rampal S

Concerns on the multiple nomenclature systems for SARS-CoV-2.

Journal of medical virology | 2022-03-01 | PMID 34672373

Li Xingguang

Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.

Genetic epidemiology | 2022-02-01 | PMID 34672391

Grace Christopher, Hopewell Jemma C, Watkins Hugh and 2 more

Contributions of NFKB1 -94insertion/deletion ATTG polymorphism to the susceptibility of gastrointestinal cancers: A meta-analysis.

Journal of cellular and molecular medicine | 2021-11-01 | PMID 34672421

Wu Hanqiang, Liang Jianrong

Increasing life expectancy in cystic fibrosis: Advances and challenges.

Pediatric pulmonology | 2022-02-01 | PMID 34672432

McBennett Kimberly A, Davis Pamela B, Konstan Michael W

Airway clearance and exercise for people with cystic fibrosis: Balancing longevity with life.

Pediatric pulmonology | 2022-02-01 | PMID 34672434

Rowbotham Nicola J, Daniels Tracey E

A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus.

Molecular genetics & genomic medicine | 2021-11-01 | PMID 34672437

Chesneau Bertrand, Plancke Aurélie, Rolland Guillaume and 9 more

Development of a Single Quantum Dot-Mediated FRET Nanosensor for Sensitive Detection of Single-Nucleotide Polymorphism in Cancer Cells.

Analytical chemistry | 2021-11-02 | PMID 34672523

Li Chen-Chen, Hu Jinping, Luo Xiliang and 2 more

A Phenotypic Screen Identifies a Compound Series That Induces Differentiation of Acute Myeloid Leukemia Cells In Vitro and Shows Antitumor Effects In Vivo.

Journal of medicinal chemistry | 2021-11-11 | PMID 34672555

Josa-Culleré Laia, Madden Katrina S, Cogswell Thomas J and 9 more

Direct Detection of Low Abundance Genes of Single Point Mutation.

Nano letters | 2021-11-10 | PMID 34672610

Mishra Sourav, Jeon Jinseong, Kang Jun-Kyu and 7 more

Genetic polymorphisms in the mEH gene in relation to tobacco smoking: role in lung cancer susceptibility and survival in north Indian patients with lung cancer undergoing platinum-based chemotherapy.

Future oncology (London, England) | 2021-12-01 | PMID 34672683

Walia Harleen Kaur, Singh Navneet, Sharma Siddharth

Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2021-12-10 | PMID 34672684

Yadav Siddhartha, Hu Chunling, Nathanson Katherine L and 39 more

AGO2 expression levels and related genetic polymorphisms: influence in renal cell progression and aggressive phenotypes.

Pharmacogenomics | 2021-11-01 | PMID 34672687

Teixeira Ana Luísa, Patrão Ana Sofia, Dias Francisca and 7 more

Molecular Pathology of Laminopathies.

Annual review of pathology | 2022-01-24 | PMID 34672689

Shin Ji-Yeon, Worman Howard J