Genetic screening of children with marrow failure. The role of primary Immunodeficiencies.
American journal of hematology | 2021-09-01 | PMID 34000087
Miano Maurizio, Grossi Alice, Dell'Orso Gianluca and 14 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 8567 of 10600
SHIRPA as a Neurological Screening Battery in Mice.
Current protocols | 2021-05-01 | PMID 34000103
Lalonde Robert, Filali Mohammed, Strazielle Catherine
Maternal serotonin transporter genotype and offsprings' clinical and cognitive measures of ADHD and ASD.
Progress in neuro-psychopharmacology & biological psychiatry | 2021-08-30 | PMID 34000292
Hanswijk Sabrina I, van Rooij Daan, Oosterlaan Jaap and 7 more
The evolving art of creating genetic diversity: From directed evolution to synthetic biology.
Biotechnology advances | 2000-01-01 | PMID 34000294
Currin Andrew, Parker Steven, Robinson Christopher J and 3 more
Regulation of Wnt receptor activity: Implications for therapeutic development in colon cancer.
The Journal of biological chemistry | 2000-01-01 | PMID 34000297
Zhong Zhendong A, Michalski Megan N, Stevens Payton D and 2 more
Attractin Gene Deficiency in Rats Leads to Impairments in Both Activity and Spatial Learning and Memory.
Neuroscience | 2021-07-01 | PMID 34000322
Li Xiao-Hui, Xue Cheng, Liu Meng-Qi and 7 more
Understanding pain perception through genetic painlessness diseases: The role of NGF and proNGF.
Pharmacological research | 2021-07-01 | PMID 34000361
Testa Giovanna, Cattaneo Antonino, Capsoni Simona
Increased Wheat Protein Content via Introgression of an HMW Glutenin Selectively Reshapes the Grain Proteome.
Molecular & cellular proteomics : MCP | 2021-01-01 | PMID 34000434
Cao Hui, Duncan Owen, Islam Shahidul and 3 more
Seven patients with Smith-McCort dysplasia 2: Four novel nonsense variants in RAB33B and follow-up findings.
European journal of medical genetics | 2021-07-01 | PMID 34000439
Tüysüz Beyhan, Geyik Filiz, Yıldırım Timur and 3 more
Management of CLN1 Disease: International Clinical Consensus.
Pediatric neurology | 2021-07-01 | PMID 34000449
Augustine Erika F, Adams Heather R, de Los Reyes Emily and 15 more
Genes: PPT1
Colorectal cancer risk in families with Birt-Hogg-Dubé syndrome increased.
European journal of cancer (Oxford, England : 1990) | 2021-07-01 | PMID 34000505
Sattler Elke C, Syunyaeva Zulfiya, Reithmair Marlene and 2 more
Impact of the spirometric definition on comorbidities in chronic obstructive pulmonary disease.
Respiratory medicine | 2021-08-01 | PMID 34000574
Meteran Howraman, Thomsen Simon Francis, Miller Martin R and 3 more
Association of adipocytokine IL-1A and IL-6 genes with intramuscular fat content and fatty acid composition in pigs.
Meat science | 2021-09-01 | PMID 34000609
Pothakam Nanthana, Supakankul Pantaporn, Norseeda Worrarak and 6 more
Deep learning predicts gene expression as an intermediate data modality to identify susceptibility patterns in Mycobacterium tuberculosis infected Diversity Outbred mice.
EBioMedicine | 2021-05-01 | PMID 34000621
Tavolara Thomas E, Niazi M K K, Gower Adam C and 3 more
Distinct clinical and genetic mutation characteristics in sporadic and Lynch syndrome-associated endometrial cancer in a Chinese population.
Cancer epidemiology | 2021-08-01 | PMID 34000661
Sun Peisong, Shen Yan, Wang Tian and 5 more
MTHFR 677T-1298C haplotype in acute lymphoblastic leukemia: Impact on methotrexate therapy.
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners | 2022-07-01 | PMID 34000920
Frikha Rim, Elloumi Moez, Rebai Tarek and 1 more
Influence of UGT2B7 and UGT1A6 polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children.
Xenobiotica; the fate of foreign compounds in biological systems | 2021-07-01 | PMID 34000957
Du Zhaosong, Xu Hua, Zhao Peiwei and 3 more
Val66Met polymorphism is associated with decreased likelihood for pediatric headache and migraine.
Neurological research | 2021-09-01 | PMID 34000980
Koute Vasiliki, Michalopoulou Amalia, Siokas Vasileios and 9 more
Estimating colocalization probability from limited summary statistics.
BMC bioinformatics | 2021-05-17 | PMID 34000989
King Emily A, Dunbar Fengjiao, Davis Justin Wade and 1 more
Single nucleotide polymorphisms reveal genetic diversity in New Mexican chile peppers (Capsicum spp.).
BMC genomics | 2021-05-17 | PMID 34000992
Lozada Dennis N, Bhatta Madhav, Coon Danise and 1 more
Genome-wide detection of CNVs and their association with performance traits in broilers.
BMC genomics | 2021-05-17 | PMID 34001004
Fernandes Anna Carolina, da Silva Vinicius Henrique, Goes Carolina Purcell and 8 more
Genetic diversity of Coxsackievirus A21 associated with sporadic cases of acute respiratory infections in Malaysia.
BMC infectious diseases | 2021-05-17 | PMID 34001016
Supian Nur Izzati, Ng Kim Tien, Chook Jack Bee and 3 more
PRICKLE1, a Wnt/PCP signaling component, is overexpressed and associated with inferior prognosis in acute myeloid leukemia.
Journal of translational medicine | 2021-05-17 | PMID 34001134
Jiang Duanfeng, He Yanjuan, Mo Qiuyu and 7 more
Cdk5 regulatory subunit-associated protein 1 knockout mice show hearing loss phenotypically similar to age-related hearing loss.
Molecular brain | 2021-05-17 | PMID 34001214
Miwa Toru, Wei Fan-Yan, Tomizawa Kazuhito
The Comprehensive Autistic Trait Inventory (CATI): development and validation of a new measure of autistic traits in the general population.
Molecular autism | 2021-05-17 | PMID 34001225
English Michael C W, Gignac Gilles E, Visser Troy A W and 3 more
Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy.
Orphanet journal of rare diseases | 2021-05-17 | PMID 34001227
Garcia-Delgado Ana B, Valdes-Sanchez Lourdes, Morillo-Sanchez Maria Jose and 3 more
Prevalence of IGFBP3, NOS3 and TCF7L2 polymorphisms and their association with hypertension: a population-based study with Brazilian women of African descent.
BMC research notes | 2021-05-17 | PMID 34001234
Neto Abel Barbosa Lira, Vasconcelos Nancy Borges Rodrigues, Dos Santos Tamara Rodrigues and 4 more
Are caveolin-1 minor alleles more likely to be risk alleles in insulin resistance mechanisms in metabolic diseases?
BMC research notes | 2021-05-17 | PMID 34001235
Abaj Faezeh, Saeedy Said Abdul Ghafour, Mirzaei Khadijeh
An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.
Genome medicine | 2021-05-17 | PMID 34001247
Wang Liuyang, Balmat Thomas J, Antonia Alejandro L and 13 more
Genes: ABO, CD209, DPP9
Initial study on TMPRSS2 p.Val160Met genetic variant in COVID-19 patients.
Human genomics | 2021-05-17 | PMID 34001248
Wulandari Laksmi, Hamidah Berliana, Pakpahan Cennikon and 14 more
The genomic distribution map of human papillomavirus in Western China.
Epidemiology and infection | 2021-05-18 | PMID 34001298
Chen Ling, Dong Yan, Li Jiao and 8 more
Validating the revised Symptom Impact Questionnaire with a proposed fibromyalgia phenotype using experimentally-induced pain and patient self-reports.
Clinical and experimental rheumatology | 2000-01-01 | PMID 34001310
Friend Ronald, Bennett Robert M, Aebischer Jonathan H and 2 more
Multi-step vs. single-step resistance evolution under different drugs, pharmacokinetics, and treatment regimens.
eLife | 2021-05-18 | PMID 34001313
Igler Claudia, Rolff Jens, Regoes Roland
Genomic evaluation of dairy heifer livability.
Journal of dairy science | 2021-08-01 | PMID 34001366
Neupane M, Hutchison J L, Van Tassell C P and 1 more
Clinical and epidemiological features of tuberculosis isolated from critically ill patients.
Revista Argentina de microbiologia | 2000-01-01 | PMID 34001412
Hurtado Joaquín, Coitinho Cecilia, Nin Nicolás and 4 more
An instantaneous coalescent method insensitive to population structure.
Journal of genetics and genomics = Yi chuan xue bao | 2021-03-20 | PMID 34001433
Yao Zeqi, Liu Kehui, Deng Shanjun and 1 more
Psoriasis is a disease of the entire skin: non-lesional skin displays a prepsoriasis phenotype.
European journal of dermatology : EJD | 2021-04-01 | PMID 34001466
Nosbaum Audrey, Dahel Karima, Goujon Catherine and 3 more
Staphylococcus aureus Peptide Methionine Sulfoxide Reductases Protect from Human Whole-Blood Killing.
Infection and immunity | 2021-07-15 | PMID 34001560
Beavers William N, DuMont Ashley L, Monteith Andrew J and 9 more
G-quadruplex structural variations in human genome associated with single-nucleotide variations and their impact on gene activity.
Proceedings of the National Academy of Sciences of the United States of America | 2021-05-25 | PMID 34001600
Gong Jia-Yuan, Wen Cui-Jiao, Tang Ming-Liang and 9 more
Genomic basis of parallel adaptation varies with divergence in Arabidopsis and its relatives.
Proceedings of the National Academy of Sciences of the United States of America | 2021-05-25 | PMID 34001609
Bohutínská Magdalena, Vlček Jakub, Yair Sivan and 5 more
Reconstitution of β-adrenergic regulation of CaV1.2: Rad-dependent and Rad-independent protein kinase A mechanisms.
Proceedings of the National Academy of Sciences of the United States of America | 2021-05-25 | PMID 34001616
Katz Moshe, Subramaniam Suraj, Chomsky-Hecht Orna and 6 more
Detection of differentially abundant cell subpopulations in scRNA-seq data.
Proceedings of the National Academy of Sciences of the United States of America | 2021-06-01 | PMID 34001664
Zhao Jun, Jaffe Ariel, Li Henry and 6 more
Clinicopathologic and Genomic Characterization of Inflammatory Myofibroblastic Tumors of the Head and Neck: Highlighting a Novel Fusion and Potential Diagnostic Pitfall.
The American journal of surgical pathology | 2021-12-01 | PMID 34001695
Kerr Darcy A, Thompson Lester D R, Tafe Laura J and 14 more
Contribution of lncRNA CASC8, CASC11, and PVT1 Genetic Variants to the Susceptibility of Coronary Heart Disease.
Journal of cardiovascular pharmacology | 2021-06-01 | PMID 34001726
Lu Yan, Yuan Wei, Wang Lan and 6 more
ADULT-ONSET BEST1 -VITELLIFORM DYSTROPHY ASSOCIATED WITH ANGIOID STREAK-LIKE CHANGES IN TWO SIBLINGS.
Retinal cases & brief reports | 2023-05-01 | PMID 34001763
Li Yafeng, Bracha Peter, Aleman Tomas S and 1 more
Birth weight, childhood obesity and risk of hypertension: a Mendelian randomization study.
Journal of hypertension | 2021-09-01 | PMID 34001814
Fan Jingwen, Shi Xuezhong, Jia Xiaocan and 5 more
ISOLATED MACULOPATHY AND MODERATE ROD-CONE DYSTROPHY REPRESENT THE MILDER END OF THE RDH12-RELATED RETINAL DYSTROPHY SPECTRUM.
Retina (Philadelphia, Pa.) | 2021-06-01 | PMID 34001834
De Zaeytijd Julie, Van Cauwenbergh Caroline, De Bruyne Marieke and 4 more
ACE2 polymorphism and susceptibility for SARS-CoV-2 infection and severity of COVID-19.
Pharmacogenetics and genomics | 2021-10-01 | PMID 34001841
Möhlendick Birte, Schönfelder Kristina, Breuckmann Katharina and 21 more
ZNF423 modulates the AMP-activated protein kinase pathway and metformin response in a single nucleotide polymorphisms, estrogen and selective estrogen receptor modulator dependent fashion.
Pharmacogenetics and genomics | 2021-09-01 | PMID 34001842
Qin Sisi, Ingle James N, Kim Wootae and 3 more
Circulating biomarkers of immunity and inflammation, risk of Alzheimer's disease, and hippocampal volume: a Mendelian randomization study.
Translational psychiatry | 2021-05-17 | PMID 34001857
Fani Lana, Georgakis Marios K, Ikram M Arfan and 3 more
Assessing olfactory, memory, social and circadian phenotypes associated with schizophrenia in a genetic model based on Rim.
Translational psychiatry | 2021-05-17 | PMID 34001859
Hidalgo Sergio, Campusano Jorge M, Hodge James J L
A global resource for genomic predictions of antimicrobial resistance and surveillance of Salmonella Typhi at pathogenwatch.
Nature communications | 2021-05-17 | PMID 34001879
Argimón Silvia, Yeats Corin A, Goater Richard J and 15 more
Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits.
Nature communications | 2021-05-17 | PMID 34001886
Zhao Bingxin, Shan Yue, Yang Yue and 9 more
The paradox of retained genetic diversity of Hippocampus guttulatus in the face of demographic decline.
Scientific reports | 2021-05-17 | PMID 34001923
Stacy Rupert, Palma Jorge, Correia Miguel and 3 more
CRISPR-mediated mutations in the ABC transporter gene ABCA2 confer pink bollworm resistance to Bt toxin Cry2Ab.
Scientific reports | 2021-05-17 | PMID 34001946
Fabrick Jeffrey A, LeRoy Dannialle M, Mathew Lolita G and 6 more
Radiation inducible MafB gene is required for thymic regeneration.
Scientific reports | 2021-05-17 | PMID 34001954
Hashimoto Daiki, Colet Jose Gabriel R, Murashima Aki and 9 more
Genetic structure of urban and non-urban populations differs between two common parid species.
Scientific reports | 2021-05-17 | PMID 34001959
Markowski Marcin, Minias Piotr, Bańbura Mirosława and 6 more
TERTp mutations and p53 expression in head and neck cutaneous basal cell carcinomas with different aggressive features.
Scientific reports | 2021-05-17 | PMID 34001963
Castanheira António, Vieira Maria João, Pinto Mafalda and 9 more
Identification of a PadR-type regulator essential for intracellular pathogenesis of Burkholderia pseudomallei.
Scientific reports | 2021-05-17 | PMID 34001967
McMillan Ian A, Norris Michael H, Zarzycki-Siek Jan and 4 more
Complement C5 is not critical for the formation of sub-RPE deposits in Efemp1 mutant mice.
Scientific reports | 2021-05-17 | PMID 34001980
Garland Donita L, Pierce Eric A, Fernandez-Godino Rosario
Genetic polymorphism of interleukin-1 receptor antagonist in Type 1 diabetic children.
Pediatric research | 2022-05-01 | PMID 34002010
Abed Neveen T, Ramadan Ismail A, Mohammed Shuzan A and 1 more
Characterization of the human TARDBP gene promoter.
Scientific reports | 2021-05-17 | PMID 34002018
Baralle Marco, Romano Maurizio
Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probands.
Molecular psychiatry | 2022-01-01 | PMID 34002022
Pugsley Kealan, Scherer Stephen W, Bellgrove Mark A and 1 more
Selection of metastasis competent subclones in the tumour interior.
Nature ecology & evolution | 2021-07-01 | PMID 34002049
Zhao Yue, Fu Xiao, Lopez Jose I and 23 more
The language of chromatin modification in human cancers.
Nature reviews. Cancer | 2021-07-01 | PMID 34002060
Zhao Shuai, Allis C David, Wang Gang Greg
Pancreatic cancer epidemiology: understanding the role of lifestyle and inherited risk factors.
Nature reviews. Gastroenterology & hepatology | 2021-07-01 | PMID 34002083
Klein Alison P
An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank.
Nature genetics | 2021-07-01 | PMID 34002094
Yonova-Doing Ekaterina, Calabrese Claudia, Gomez-Duran Aurora and 5 more
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nature genetics | 2021-06-01 | PMID 34002096
Mullins Niamh, Forstner Andreas J, O'Connell Kevin S and 314 more
Mutant-TMEM230-induced neurodegeneration and impaired axonal mitochondrial transport.
Human molecular genetics | 2021-07-28 | PMID 34002226
Wang Xiaobo, Guo Gongbo, Zhang Jinru and 5 more
A 24,482-bp deletion is associated with increased seed weight in Brassica napus L.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2021-08-01 | PMID 34002254
Zhang Xiaohui, Huang Qiyang, Wang Pengfei and 7 more
Distribution of genotypes in relation to metronidazole susceptibility patterns in Trichomonas vaginalis isolated from South African pregnant women.
Parasitology research | 2021-06-01 | PMID 34002261
Mabaso Nonkululeko, Abbai Nathlee
Influence of FecGE mutation on the reproductive variables of Pelibuey ewes in the anestrus period.
Tropical animal health and production | 2021-05-17 | PMID 34002300
Muñoz-García Canuto, Vaquera-Huerta Humberto, Gallegos-Sánchez Jaime and 4 more
Cerebral folate transporter deficiency: a potentially treatable neurometabolic disorder.
Acta neurologica Belgica | 2023-02-01 | PMID 34002331
Kanmaz Seda, Simsek Erdem, Yilmaz Sanem and 3 more
Traditional System Versus DNA Barcoding in Identification of Bamboo Species: A Systematic Review.
Molecular biotechnology | 2021-08-01 | PMID 34002354
Sawarkar Ankush D, Shrimankar Deepti D, Kumar Manish and 3 more
Digest: On the contribution of phenotypic plasticity to adaptation in desert environments.
Evolution; international journal of organic evolution | 2021-06-01 | PMID 34002385
Narayan Vikram P
Identification of genes associated with litter size combining genomic approaches in Luzhong mutton sheep.
Animal genetics | 2021-08-01 | PMID 34002409
Tao L, He X Y, Wang F Y and 5 more
Giant nevus comedonicus of the entire lower left limb protecting from the associated bullous pemphigoid: A hypothetical role of NEK9 mutation?
The Journal of dermatology | 2021-08-01 | PMID 34002421
Herzum Astrid, Cozzani Emanuele, Micalizzi Claudia and 3 more
Neuropathology of the spinal nerve roots, spinal cord, and brain in the first autopsied case of Charcot-Marie-Tooth disease 4F with a D651N mutation in the periaxin gene.
Neuropathology : official journal of the Japanese Society of Neuropathology | 2021-08-01 | PMID 34002422
Shintaku Masayuki, Maeda Kengo, Shiohara Masanori and 2 more
BRCA mutation carriers' perceptions on postmenopausal hormone therapy: An Italian study.
Psycho-oncology | 2021-10-01 | PMID 34002428
Grandi Giovanni, Boggio Sola Valentina, Cortesi Laura and 4 more
Profiling beneficial and potential adverse effects of MeCP2 overexpression in a hypomorphic Rett syndrome mouse model.
Genes, brain, and behavior | 2022-01-01 | PMID 34002468
Vermudez Sheryl Anne D, Gogliotti Rocco G, Arthur Bright and 6 more
Loss-of-function variants in Kv 11.1 cardiac channels as a biomarker for SUDEP.
Annals of clinical and translational neurology | 2021-07-01 | PMID 34002542
Soh Ming S, Bagnall Richard D, Bennett Mark F and 12 more
PD-L1 SNPs as biomarkers to define benefit in patients with advanced NSCLC treated with immune checkpoint inhibitors.
Tumori | 2022-02-01 | PMID 34002648
Minari Roberta, Bonatti Francesco, Mazzaschi Giulia and 15 more
Evaluation of hepatitis E antigen kinetics and its diagnostic utility for prediction of the outcomes of hepatitis E virus genotype 1 infection.
Virulence | 2021-12-01 | PMID 34002677
El-Mokhtar Mohamed A, Karam-Allah Ramadan Haidi, Abdel Hameed Muhamad R and 9 more
Polymerization of misfolded Z alpha-1 antitrypsin protein lowers CX3CR1 expression in human PBMCs.
eLife | 2021-05-18 | PMID 34002692
Tumpara Srinu, Ballmaier Matthias, Wrenger Sabine and 12 more
Deleterious mutation V369M in the mouse GCGR gene causes abnormal plasma amino acid levels indicative of a possible liver-α-cell axis.
Bioscience reports | 2021-06-25 | PMID 34002801
Liu Qiaofeng, Lin Guangyao, Chen Yan and 5 more
Serum lipid and adiponectin/leptin ratio changes after a Mediterranean dietary pattern in non-g-allele carriers of the genetic variant of adiponectin gene rs822393.
European review for medical and pharmacological sciences | 2021-05-01 | PMID 34002823
Primo D, Izaola O, de Luis D
Pediatric problematic severe asthma: Recent advances in management.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2021-10-01 | PMID 34002877
Scotney Elizabeth, Burchett Saskia, Goddard Thomas and 1 more
Rational Design of Novel Therapies for Pantothenate Kinase-Associated Neurodegeneration.
Movement disorders : official journal of the Movement Disorder Society | 2021-09-01 | PMID 34002881
Thakur Nivedita, Klopstock Thomas, Jackowski Suzanne and 4 more
Genes: PANK2
Natural nest substrates influence squamate embryo physiology but have little effect on hatchling phenotypes.
Integrative zoology | 2022-07-01 | PMID 34002932
Hall Joshua M, Miracle Jocelyn, Scruggs Cindy D and 1 more
The delineation of the Wolf-Hirschhorn syndrome over six decades: Illustration of the ongoing advances in phenotype analysis and cytogenomic technology.
American journal of medical genetics. Part A | 2021-09-01 | PMID 34002939
Battaglia Agatino, Carey John C
Prevalence of oncogenic human papillomavirus in patients with cervical lesion.
Revista medica del Instituto Mexicano del Seguro Social | 2020-05-18 | PMID 34002982
Juárez-González Karina, Paredes-Cervantes Vladimir, Martínez-Salazar Martha and 5 more
Implementation of a next-generation sequencing-based targeted approach for full-length CYP3A4 gene sequencing.
Pharmacogenomics | 2021-06-01 | PMID 34003019
Kivrane Agnija, Igumnova Viktorija, Kimsis Janis and 5 more
The association of glutathione S-transferase T1 and M1 deletions with myocardial infarction.
Free radical research | 2021-03-01 | PMID 34003050
Zivkovic Maja, Bubic Maja, Kolakovic Ana and 4 more
Corneal ectasia associated with posterior lamellar opacification.
Ophthalmic genetics | 2021-08-01 | PMID 34003075
Yung Madeline, Chen Angela C, Chung Doug D and 5 more
[Newborn screening for cystic fibrosis in France].
Medecine sciences : M/S | 2021-05-01 | PMID 34003095
Munck Anne, Cheillan David, Audrezet Marie-Pierre and 2 more
Reproductive history determines Erbb2 locus amplification, WNT signalling and tumour phenotype in a murine breast cancer model.
Disease models & mechanisms | 2021-05-01 | PMID 34003256
Ordonez Liliana D, Melchor Lorenzo, Greenow Kirsty R and 5 more
Comparative Genomics Reveals Factors Associated with Phenotypic Expression of Wolbachia.
Genome biology and evolution | 2021-07-06 | PMID 34003269
Baião Guilherme Costa, Janice Jessin, Galinou Maria and 1 more
The Effectiveness and Safety of Hyperbaric Oxygen Therapy in Various Phenotypes of Inflammatory Bowel Disease: Systematic Review With Meta-analysis.
Inflammatory bowel diseases | 2022-03-30 | PMID 34003289
McCurdy Jeffrey, Siw Kevin Chin Koon, Kandel Rana and 3 more
Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors.
Acta neuropathologica | 2021-08-01 | PMID 34003336
Pathak Rajiv, Zin Francesca, Thomas Christian and 16 more
Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome.
Calcified tissue international | 2021-11-01 | PMID 34003338
Al Kaissi Ali, Misof Barbara M, Laccone Franco and 7 more