Exploring the association between specific genes and the onset of idiopathic scoliosis: a systematic review.
BMC medical genomics | 2022-05-19 | PMID 35590413
De Salvatore Sergio, Ruzzini Laura, Longo Umile Giuseppe and 5 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 8911 of 10600
Histone H3.3 K27M chromatin functions implicate a network of neurodevelopmental factors including ASCL1 and NEUROD1 in DIPG.
Epigenetics & chromatin | 2022-05-19 | PMID 35590427
Lewis Nichole A, Klein Rachel Herndon, Kelly Cailin and 2 more
Global distribution of Echinococcus granulosus genotypes in domestic and wild canids: a systematic review and meta-analysis.
Parasitology | 2022-08-01 | PMID 35591776
Shams Morteza, Khazaei Sasan, Naserifar Razi and 5 more
Aberrantly Activated APOBEC3B Is Associated With Mutant p53-Driven Refractory/Relapsed Diffuse Large B-Cell Lymphoma.
Frontiers in immunology | 2022-01-01 | PMID 35592333
Zhang Xuzhao, Wu Zhaoxing, Hao Yuanyuan and 15 more
A Novel TNFSF-Based Signature Predicts the Prognosis and Immunosuppressive Status of Lower-Grade Glioma.
BioMed research international | 2022-01-01 | PMID 35592520
Tao Rui, Liu Qi, Huang Ruoyu and 4 more
Serological and Molecular Characterization of Hepatitis B Virus Infection in Gastric Cancer.
Frontiers in cellular and infection microbiology | 2022-01-01 | PMID 35592651
Li Mengge, Wu Shusheng, Luo Huiqin and 12 more
Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma.
Disease markers | 2022-01-01 | PMID 35592705
Xiong Ying, Chen Ting, Yu Jia and 7 more
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.
Frontiers in endocrinology | 2022-01-01 | PMID 35592775
Wang Zhe, Choi Shing Wan, Chami Nathalie and 38 more
Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil.
Frontiers in endocrinology | 2022-01-01 | PMID 35592779
Abreu Gabriella de Medeiros, Tarantino Roberta Magalhães, da Fonseca Ana Carolina Proença and 9 more
Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.
Epilepsia | 2022-08-01 | PMID 35592948
Hammer Michael F, Pan Yanling, Cumbay Medhane and 6 more
NURR1-deficient mice have age- and sex-specific behavioral phenotypes.
Journal of neuroscience research | 2022-09-01 | PMID 35593070
Montarolo Francesca, Martire Serena, Chiara Francesco and 6 more
Cost-effectiveness analysis of molecular diagnosis by next-generation sequencing versus sequential single testing in metastatic non-small cell lung cancer patients from a south Spanish hospital perspective.
Expert review of pharmacoeconomics & outcomes research | 2022-09-01 | PMID 35593180
de Alava Enrique, Pareja María Jesús, Carcedo David and 3 more
Genetic polymorphisms related to muscular strength and flexibility are associated with artistic gymnastic performance in the Japanese population.
European journal of sport science | 2023-06-01 | PMID 35593181
Kumagai Hiroshi, Kaneko Tomoko, Shintake Yuko and 12 more
Anesthetic Challenges in a Patient With TANGO2 Gene Deletion, DiGeorge Syndrome, and Tetralogy of Fallot: A Case Report.
Seminars in cardiothoracic and vascular anesthesia | 2022-09-01 | PMID 35593202
Wrobleski Ivana, Gautam Nischal K, Hubbard Richard M
Killer cell immunoglobulin-like receptor (KIR) gene contents: Are they associated with cervical cancer?
Journal of medical virology | 2023-01-01 | PMID 35593263
Tembhurne Alok K, Maheshwari Amita, Warke Himangi and 5 more
The physiological cost of colour change: evidence, implications and mitigations.
The Journal of experimental biology | 2022-05-15 | PMID 35593398
Alfakih Ateah, Watt Penelope J, Nadeau Nicola J
DNA Methyl Transferase 3A (DNMT3A) Mutation Presenting as Isolated Pure Red Cell Aplasia.
Journal of investigative medicine high impact case reports | 2000-01-01 | PMID 35593442
Sidda Adarsh, Manu Gurusidda, Alsharedi Mohamed and 2 more
Gene, virulence and related regulatory mechanisms in Cryptococcus gattii.
Acta biochimica et biophysica Sinica | 2022-05-25 | PMID 35593469
Huang Yemei, Zang Xuelei, Yang Chen and 6 more
The role of staff and contaminated environmental surfaces in spreading of norovirus infection in a long-term health care facility in Italy.
Veterinaria italiana | 2021-12-31 | PMID 35593490
Aprea Giuseppe, Di Bartolo Ilaria, Monini Marina and 11 more
Polymorphism of the leptin gene in buffalo breed groups from eastern Amazon.
Veterinaria italiana | 2021-12-31 | PMID 35593502
Silva Lorena Keyse, Barbosa Elizabeth Machado, Silva Sandra Cristina Becker and 5 more
Detection of pyrethroid resistance mutations and intron variants in the voltage-gated sodium channel of Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus mosquitoes from Lao People's Democratic Republic.
Medical and veterinary entomology | 2022-12-01 | PMID 35593512
Marcombe Sebastien, Shimell Katherine, Savage Rachel and 19 more
Challenges in diagnosis and understanding of natural history of polycystic ovary syndrome.
Clinical endocrinology | 2022-08-01 | PMID 35593530
Joham Anju E, Piltonen Terhi, Lujan Marla E and 2 more
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.
American journal of medical genetics. Part A | 2022-08-01 | PMID 35593535
Vincent Krista Marie, Stavropoulos Dimitri J, Beaulieu-Bergeron Melanie and 5 more
Individualized discovery of rare cancer drivers in global network context.
eLife | 2022-05-20 | PMID 35593700
Petrov Iurii, Alexeyenko Andrey
Brief Report: Evidence of Autism Spectrum Disorder Caused by a Mutation in ATRX Gene: A Case Report.
Journal of autism and developmental disorders | 2024-01-01 | PMID 35593993
López-Garrido María-Pilar, Carrascosa-Romero María-Carmen, Montero-Hernández Minerva and 2 more
Sex and Age-Related Differences in Complement Factors Among Patients With Intermediate Age-Related Macular Degeneration.
Translational vision science & technology | 2022-05-02 | PMID 35594041
Marin A Itzam, Poppelaars Felix, Wagner Brandie D and 9 more
Prevalence of Germline Findings Among Tumors From Cancer Types Lacking Hereditary Testing Guidelines.
JAMA network open | 2022-05-02 | PMID 35594047
Yap Timothy A, Ashok Arya, Stoll Jessica and 5 more
The role of sigma factor competition in bacterial adaptation under prolonged starvation.
Microbiology (Reading, England) | 2022-05-01 | PMID 35594140
Nandy Pabitra
Mild motor impairment as prodromal state in amyotrophic lateral sclerosis: a new diagnostic entity.
Brain : a journal of neurology | 2022-10-21 | PMID 35594156
Benatar Michael, Granit Volkan, Andersen Peter M and 5 more
Genes: SOD1, FUS
Molecular evolution and structural analyses of the spike glycoprotein from Brazilian SARS-CoV-2 genomes: the impact of selected mutations.
Journal of biomolecular structure & dynamics | 2023-04-01 | PMID 35594172
Gröhs Ferrareze Patrícia Aline, Zimerman Ricardo Ariel, Franceschi Vinícius Bonetti and 3 more
Nucleotide- and Protein-Dependent Functions of Actg1.
Molecular biology of the cell | 2022-08-01 | PMID 35594181
Sundby Lauren J, Southern William M, Hawbaker Katelin M and 3 more
Risk of chronic pancreatitis in carriers of loss-of-function CTRC variants: A meta-analysis.
PloS one | 2022-01-01 | PMID 35594281
Takáts Amanda, Berke Gergő, Gede Noémi and 7 more
Genes: CP, CTRC
Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.
PloS one | 2022-01-01 | PMID 35594287
Shadrina Alexandra S, Elgaeva Elizaveta E, Stanaway Ian B and 7 more
Multiple molecular events underlie stochastic switching between 2 heritable cell states in fungi.
PLoS biology | 2022-05-01 | PMID 35594297
Ziv Naomi, Brenes Lucas R, Johnson Alexander
Loss of GBA in zebrafish leads to dopaminergic neurodegeneration, but overexpression of α-synuclein does not further worsen degeneration.
Neuroreport | 2022-05-04 | PMID 35594444
Kodera Kazuki, Matsui Noriko, Saitoh Akihiko and 1 more
Genome-wide association studies identified loci associated with both feed conversion ratio and residual feed intake in Yorkshire pigs.
Genome | 2022-07-01 | PMID 35594567
Wang Kai, Wang Shujie, Ji Xiang and 8 more
HLA-genotyping by next-generation-sequencing reveals shared and unique HLA alleles in two patients with coexisting neuromyelitis optica spectrum disorder and thymectomized myasthenia gravis: Immunological implications for mutual aetiopathogenesis?
Multiple sclerosis and related disorders | 2022-07-01 | PMID 35594634
Vakrakou Aigli, Chatzistamatiou Theofanis, Koros Christos and 10 more
Design and synthesis of proteolysis targeting chimeras (PROTACs) as an EGFR degrader based on CO-1686.
European journal of medicinal chemistry | 2022-08-05 | PMID 35594654
Li Qinlan, Guo Qian, Wang Shuyi and 4 more
Screening of highly discriminative microhaplotype markers for individual identification and mixture deconvolution in East Asian populations.
Forensic science international. Genetics | 2022-07-01 | PMID 35594656
Yu Wen-Shuai, Feng Yao-Sen, Kang Ke-Lai and 4 more
Mutational profiling of mtDNA control region reveals tumor-specific evolutionary selection involved in mitochondrial dysfunction.
EBioMedicine | 2022-06-01 | PMID 35594659
Ji Xiaoying, Guo Wenjie, Gu Xiwen and 8 more
Bidirectional Mendelian randomization to explore the causal relationships between Sleep traits, Parkinson's disease and Amyotrophic lateral sclerosis.
Sleep medicine | 2022-08-01 | PMID 35594779
Di Hongkun, Zhu Yi, Xia Wenqi and 8 more
Prognostic role of TNF alpha, LT alpha, MDR1 and codon 72 Tp53 gene polymorphisms on multiple myeloma Egyptian patients.
Leukemia research | 2022-06-01 | PMID 35594781
Hegazi Heba M, Elghonemy M S, El-Baiomy M A and 2 more
Water activity influence on the simultaneous production of DON, 3-ADON and 15-ADON by a strain of Fusarium graminearum ss of 15-ADON genotype.
International journal of food microbiology | 2022-07-16 | PMID 35594816
Ramírez Albuquerque Diana, Patriarca Andrea, Fernández Pinto Virginia
Local Adaptation and the Evolution of Genome Architecture in Threespine Stickleback.
Genome biology and evolution | 2022-05-31 | PMID 35594844
Li Qiushi, Lindtke Dorothea, Rodríguez-Ramírez Carlos and 7 more
The rs705708 A allele of the ERBB3 gene is associated with lower prevalence of diabetic retinopathy and arterial hypertension and with improved renal function in type 1 diabetic patients.
Microvascular research | 2022-09-01 | PMID 35594935
Massignam Eloísa Toscan, Dieter Cristine, Assmann Taís Silveira and 4 more
24 loci MIRU-VNTR analysis and pattern of drug resistance in pre-extensively drug resistant pulmonary tuberculosis in Bangladesh.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2022-08-01 | PMID 35595025
Monir Bayzid Bin, Sultana Sabia Shahin, Tarafder Shirin
Multiancestral polygenic risk score for pediatric asthma.
The Journal of allergy and clinical immunology | 2022-11-01 | PMID 35595084
Namjou Bahram, Lape Michael, Malolepsza Edyta and 21 more
Ubiquitin-conjugating activity by PEX4 is required for efficient protein transport to peroxisomes in Arabidopsis thaliana.
The Journal of biological chemistry | 2022-06-01 | PMID 35595097
Mano Shoji, Hayashi Yasuko, Hikino Kazumi and 3 more
The extended avian urban phenotype: anthropogenic solid waste pollution, nest design, and fitness.
The Science of the total environment | 2022-09-10 | PMID 35595141
Jagiello Zuzanna, Corsini Michela, Dylewski Łukasz and 2 more
A Comprehensive Triple-Repeat Primed PCR and a Long-Range PCR Agarose-Based Assay for Improved Genotyping of Guanine-Adenine-Adenine Repeats in Friedreich Ataxia.
The Journal of molecular diagnostics : JMD | 2022-08-01 | PMID 35595154
Jama Mohamed, Margraf Rebecca L, Yu Ping and 2 more
What have we learned from genome-wide association studies (GWAS) in Parkinson's disease?
Ageing research reviews | 2022-08-01 | PMID 35595184
Fernández-Santiago Rubén, Sharma Manu
Examining clustered somatic mutations with SigProfilerClusters.
Bioinformatics (Oxford, England) | 2022-06-27 | PMID 35595234
Bergstrom Erik N, Kundu Mousumy, Tbeileh Noura and 1 more
Evaluation of phenotype-driven gene prioritization methods for Mendelian diseases.
Briefings in bioinformatics | 2022-09-20 | PMID 35595299
Jacobsen Julius O B, Kelly Catherine, Cipriani Valentina and 2 more
Mutations in rhodopsin, endothelin B receptor, and CC chemokine receptor 5 in large animals: Modeling human diseases.
Progress in molecular biology and translational science | 2022-01-01 | PMID 35595348
Ji Ren-Lei, Tao Ya-Xiong
Melanocortin-1 receptor mutations and pigmentation: Insights from large animals.
Progress in molecular biology and translational science | 2022-01-01 | PMID 35595349
Ji Ren-Lei, Tao Ya-Xiong
Mutations in melanocortin-4 receptor: From fish to men.
Progress in molecular biology and translational science | 2022-01-01 | PMID 35595350
Tao Ya-Xiong
Diet in the Pathogenesis and Management of Crohn's Disease.
Gastroenterology clinics of North America | 2022-06-01 | PMID 35595417
Gu Phillip, Feagins Linda A
Prenatal diagnosis of de novo int22h1/int22h2-mediated Xq28 duplication syndrome involving RAB39B following a previous ambiguous genitalia pregnancy.
Taiwanese journal of obstetrics & gynecology | 2022-05-01 | PMID 35595445
Chien Yung Chen, Chen Jia Shing, Shiao Yu Ming and 1 more
Whole exome sequencing identifies a novel FRAS1 mutation and aids in vitro fertilization with preimplantation genetic diagnosis in Fraser syndrome.
Taiwanese journal of obstetrics & gynecology | 2022-05-01 | PMID 35595450
Ou Tsung-Ying, Tsai Meng-Che, Kuo Pao-Lin and 2 more
Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature.
Taiwanese journal of obstetrics & gynecology | 2022-05-01 | PMID 35595454
Qiu Zilong, Chang Wan-Ting, Chou Yu-Ching and 7 more
Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review.
Taiwanese journal of obstetrics & gynecology | 2022-05-01 | PMID 35595456
Yue Fagui, Xi Qi, Zhang Xinyue and 3 more
Computational methods to assist in the discovery of pharmacological chaperones for rare diseases.
Briefings in bioinformatics | 2022-09-20 | PMID 35595532
Scafuri Bernardina, Verdino Anna, D'Arminio Nancy and 1 more
A radiomics feature-based nomogram to predict telomerase reverse transcriptase promoter mutation status and the prognosis of lower-grade gliomas.
Clinical radiology | 2022-08-01 | PMID 35595562
Lu J, Li X, Li H
Lupus nephritis - An update on disparities affecting african americans.
Journal of the National Medical Association | 2022-06-01 | PMID 35595581
Portalatin Gilda M, Gebreselassie Surafel K, Bobart Shane A
Sofosbuvir-based therapy for late pregnant women and infants with severe chronic hepatitis C: A case series study.
Journal of medical virology | 2022-09-01 | PMID 35595682
Zeng Qing-Lei, Yu Zu-Jiang, Lv Jun and 6 more
Epithelial to mesenchymal transition influences fibroblast phenotype in colorectal cancer by altering miR-200 levels in extracellular vesicles.
Journal of extracellular vesicles | 2022-05-01 | PMID 35595718
Bhome Rahul, Emaduddin Muhammad, James Victoria and 9 more
Pirtobrutinib inhibits wild-type and mutant Bruton's tyrosine kinase-mediated signaling in chronic lymphocytic leukemia.
Blood cancer journal | 2022-05-20 | PMID 35595730
Aslan Burcu, Kismali Gorkem, Iles Lakesla R and 7 more
Gene flow in a pioneer plant metapopulation (Myricaria germanica) at the catchment scale in a fragmented alpine river system.
Scientific reports | 2022-05-20 | PMID 35595737
Fink Sabine, Hoppler-Wiedmer Andrea, Zengerer Veronika and 3 more
Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ.
Nature communications | 2022-05-20 | PMID 35595740
Hemmerle Lucas, Maier Benjamin A, Bortfeld-Miller Miriam and 4 more
Assessment of mutations on RBD in the Spike protein of SARS-CoV-2 Alpha, Delta and Omicron variants.
Scientific reports | 2022-05-20 | PMID 35595778
da Costa Clauber Henrique Souza, de Freitas Camila Auad Beltrão, Alves Cláudio Nahum and 1 more
Apparent regional differences in the spectrum of BARD1 pathogenic variants in Spanish population and importance of copy number variants.
Scientific reports | 2022-05-20 | PMID 35595798
Benito-Sánchez B, Barroso A, Fernández V and 9 more
Machine learning phenomics (MLP) combining deep learning with time-lapse-microscopy for monitoring colorectal adenocarcinoma cells gene expression and drug-response.
Scientific reports | 2022-05-20 | PMID 35595808
D'Orazio M, Murdocca M, Mencattini A and 8 more
Automated next-generation profiling of genomic alterations in human cancers.
Nature communications | 2022-05-20 | PMID 35595835
Keefer Laurel A, White James R, Wood Derrick E and 25 more
Molecular basis for gating of cardiac ryanodine receptor explains the mechanisms for gain- and loss-of function mutations.
Nature communications | 2022-05-20 | PMID 35595836
Kobayashi Takuya, Tsutsumi Akihisa, Kurebayashi Nagomi and 6 more
Proof of concept for multiplex amplicon sequencing for mutation identification using the MinION nanopore sequencer.
Scientific reports | 2022-05-20 | PMID 35595858
Whitford Whitney, Hawkins Victoria, Moodley Kriebashne S and 4 more
Segmental spinal neurofibromatosis 1: a novel phenotype.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022-08-01 | PMID 35595873
Fatima Nida, La Dine Anna, Barnard Zachary R and 1 more
The efficacy of combining topiramate and 4-aminopyridine to reduce relapses and interictal progression in two cases of episodic ataxia type 2.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022-08-01 | PMID 35595874
González-Mingot Cristina, López-Ortega Ricard, Brieva-Ruiz Luis
Genes: CACNA1A
Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.
Reproductive sciences (Thousand Oaks, Calif.) | 2022-10-01 | PMID 35595959
Hou Meiqi, Zhu Lixia, Jiang Jinghang and 11 more
Paternal nicotine taking elicits heritable sex-specific phenotypes that are mediated by hippocampal Satb2.
Molecular psychiatry | 2022-09-01 | PMID 35595980
Maurer John J, Wimmer Mathieu E, Turner Christopher A and 8 more
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation.
Journal of autism and developmental disorders | 2023-03-01 | PMID 35596027
Chow Julie C, Hormozdiari Fereydoun
Recent status of Genotyping by Sequencing (GBS) Technology in cucumber (Cucumis sativus L.): a review.
Molecular biology reports | 2022-06-01 | PMID 35596053
Nyirahabimana Fildaus, Shimira Flavien, Zahid Ghassan and 1 more
Loss of RTN3 phenocopies chronic kidney disease and results in activation of the IGF2-JAK2 pathway in proximal tubular epithelial cells.
Experimental & molecular medicine | 2022-05-01 | PMID 35596061
Fan Liang-Liang, Du Ran, Liu Ji-Shi and 6 more
A comprehensive study on size and definition of the core group in the proven and young algorithm for single-step GBLUP.
Genetics, selection, evolution : GSE | 2022-05-20 | PMID 35596130
Abdollahi-Arpanahi Rostam, Lourenco Daniela, Misztal Ignacy
Recombination rates in pigs differ between breeds, sexes and individuals, and are associated with the RNF212, SYCP2, PRDM7, MEI1 and MSH4 loci.
Genetics, selection, evolution : GSE | 2022-05-20 | PMID 35596132
Brekke Cathrine, Berg Peer, Gjuvsland Arne B and 1 more
Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.).
BMC plant biology | 2022-05-21 | PMID 35596150
Zhao Yue, Sun Yufeng, Cao Kun and 6 more
Genomic features of Chinese small cell lung cancer.
BMC medical genomics | 2022-05-20 | PMID 35596192
Liu Jun, Zhao Zhuxiang, Wei Shuquan and 2 more
Detection of novel variant and functional study in a Chinese family with nonsyndromic oligodontia.
Oral diseases | 2023-07-01 | PMID 35596231
Sun Ruiqing, Li Shuangying, Xia Bin and 1 more
Population Genetic Characteristics and Mating Type Frequency of Venturia effusa from Pecan in South America.
Phytopathology | 2022-10-01 | PMID 35596236
Bock Clive H, Frusso Enrique, Zoppolo Roberto and 5 more
Behavioural and morphological traits influence sex-specific floral resource use by hummingbirds.
The Journal of animal ecology | 2022-11-01 | PMID 35596605
Maglianesi María A, Maruyama Pietro K, Temeles Ethan J and 14 more
[Clinical aspects of the effectiveness of metformin therapy in combination with a low-calorie diet in patients with type 2 diabetes mellitus with various variants of the TCF7L2 gene polymorphism].
Voprosy pitaniia | 2022-01-01 | PMID 35596630
Kondratyeva O V, Sharafetdinov Kh Kh, Plotnikova O A and 4 more
[The role of polymorphic variants rs11546155 and rs6119534 of the GGT7 gene and risk factors in the development of acute pancreatitis].
Voprosy pitaniia | 2022-01-01 | PMID 35596634
Samgina T A, Lazarenko V A
The p.P1127S pathogenic variant lowers von Willebrand factor levels through higher affinity for the macrophagic scavenger receptor LRP1: Clinical phenotype and pathogenic mechanisms.
Journal of thrombosis and haemostasis : JTH | 2022-08-01 | PMID 35596664
Sacco Monica, Lancellotti Stefano, Branchini Alessio and 8 more
Genetics of Cushing's disease.
Journal of neuroendocrinology | 2022-08-01 | PMID 35596671
Simon Julia, Theodoropoulou Marily
First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1.
American journal of medical genetics. Part A | 2022-08-01 | PMID 35596688
Danda Sumita, Datar Chaitanya, Kher Archana and 3 more
Evolution of selfing syndrome and its influence on genetic diversity and inbreeding: A range-wide study in Oenothera primiveris.
American journal of botany | 2022-05-01 | PMID 35596689
Cisternas-Fuentes Anita, Jogesh Tania, Broadhead Geoffrey T and 3 more
Trafficking of the glutamate transporter is impaired in LRRK2-related Parkinson's disease.
Acta neuropathologica | 2022-07-01 | PMID 35596783
Iovino Ludovica, Giusti Veronica, Pischedda Francesca and 18 more
BRCA1 and BRCA2 screening of nine Chilean founder mutations through allelic-discrimination and real-time PCR in breast/ovarian cancer patients.
Molecular biology reports | 2022-08-01 | PMID 35596815
Alvarez Carolina, Ortega-Hernández Victoria, Cortez Aracely and 1 more
Timely cancer genetic counseling and testing for young women with breast cancer: impact on surgical decision-making for contralateral risk-reducing mastectomy.
Breast cancer research and treatment | 2022-07-01 | PMID 35596825
Sanoba Shenin A, Thull Darcy L, McAuliffe Priscilla F and 4 more
Sensory and Social Subtypes of Japanese Individuals with Autism Spectrum Disorders.
Journal of autism and developmental disorders | 2023-08-01 | PMID 35596829
Kaneko Ayako, Ohshima Remi, Noda Haruka and 3 more
Combined Immunodeficiency Caused by a Novel De Novo Gain-of-Function RAC2 Mutation.
Journal of clinical immunology | 2022-08-01 | PMID 35596857
Zhang Liang, Chen Zhi, Li Wenyan and 11 more