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 8915 of 10600

Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report.
Hematology (Amsterdam, Netherlands) | 2022-12-01 | PMID 35617302
Park Joonhong, Yhim Ho-Young, Kang Kyung Pyo and 2 more
Circulating microRNA-122 in HCV cirrhotic patients with high frequency of genotype 3.
PloS one | 2022-01-01 | PMID 35617369
Ullah Amin, Yu Xiaojie, Odenthal Margarete and 6 more
How full is the evolutionary fuel tank?
Science (New York, N.Y.) | 2022-05-27 | PMID 35617388
Walsh Bruce
Genetic variance in fitness indicates rapid contemporary adaptive evolution in wild animals.
Science (New York, N.Y.) | 2022-05-27 | PMID 35617403
Bonnet Timothée, Morrissey Michael B, de Villemereuil Pierre and 37 more
Reduced physiological plasticity in a fish adapted to stable temperatures.
Proceedings of the National Academy of Sciences of the United States of America | 2022-05-31 | PMID 35617428
Morgan Rachael, Andreassen Anna H, Åsheim Eirik R and 6 more
The enigmatic tropical alpine flora on the African sky islands is young, disturbed, and unsaturated.
Proceedings of the National Academy of Sciences of the United States of America | 2022-05-31 | PMID 35617436
Kandziora Martha, Gehrke Berit, Popp Magnus and 3 more
A 2-bp deletion mutation in SMPD1 gene leading to lysosomal acid sphingomyelinase deficiency in a Chinese consanguineous pedigree.
Journal of pediatric endocrinology & metabolism : JPEM | 2022-08-26 | PMID 35617710
Kang Han, Zhou Min, Xie Chengxiu and 1 more
PTPN11 mutations in adult acute myeloid leukaemia: Prevalence and clinical implications in the context of NPM1 mutation.
Leukemia research | 2022-07-01 | PMID 35617714
Liu Jie, Qin Wei, Wang Biao and 7 more
SPG11 presenting with dystonic tremor in childhood.
Parkinsonism & related disorders | 2022-06-01 | PMID 35617747
Innes Emily A, Goetti Robert, Mahant Neil and 5 more
The effect of sickle cell genotype on the pharmacokinetic properties of artemether-lumefantrine in Tanzanian children.
International journal for parasitology. Drugs and drug resistance | 2022-08-01 | PMID 35617818
Sugiarto Sri Riyati, Bwire George M, Moore Brioni R and 8 more
Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q.
EBioMedicine | 2022-06-01 | PMID 35617825
Adema Vera, Palomo Laura, Walter Wencke and 17 more
Generation of isogenic control DJ-1-delP GC13 for the genetic Parkinson's disease-patient derived iPSC line DJ-1-delP (LCSBi008-A-1).
Stem cell research | 2022-07-01 | PMID 35617842
Mencke Pauline, Hanss Zoé, Jarazo Javier and 9 more
Plppr5 gene inactivation causes a more severe neurological phenotype and abnormal mitochondrial homeostasis in a mouse model of juvenile seizure.
Epilepsy research | 2022-07-01 | PMID 35617916
Wang Dandan, Liu Yueying, Zhao Dongjing and 3 more
Joint Effect of Multiple Prothrombotic Genotypes and Mean Platelet Volume on the Risk of Incident Venous Thromboembolism.
Thrombosis and haemostasis | 2022-11-01 | PMID 35617954
Jakobsen Lisa, Frischmuth Tobias, Brækkan Sigrid K and 2 more
Haploinsufficiency of PRRT2 Leading to Familial Hemiplegic Migraine in Chromosome 16p11.2 Deletion Syndrome.
Neuropediatrics | 2022-08-01 | PMID 35617967
Sen Kuntal, Genser Ilyse, DiFazio Marc and 1 more
Nonalcoholic fatty liver disease and cardiovascular diseases: A Mendelian randomization study.
Metabolism: clinical and experimental | 2022-08-01 | PMID 35618017
Peng Hexiang, Wang Siyue, Wang Mengying and 13 more
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologists.
European journal of medical genetics | 2022-07-01 | PMID 35618197
McTague Amy, Brunklaus Andreas, Barcia Giulia and 7 more
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.
European journal of medical genetics | 2022-07-01 | PMID 35618198
Kamal Neda, Khamirani Hossein Jafari, Mohammadi Sanaz and 3 more
Investigation on a MMACHC mutant from cblC disease: The c.394C>T variant.
Biochimica et biophysica acta. Proteins and proteomics | 2022-06-01 | PMID 35618206
Passantino Rosa, Mangione Maria Rosalia, Ortore Maria Grazia and 7 more
Using comparative genomics to detect mutations regulating plumage variations in graylag (A. anser) and swan geese (A. cygnoides).
Gene | 2022-08-05 | PMID 35618220
Yang Yunzhou, Wang Huiying, Li Guangquan and 7 more
The applications of plasma cell-free DNA in cancer detection: Implications in the management of breast cancer patients.
Critical reviews in oncology/hematology | 2022-07-01 | PMID 35618229
Igari Fumie, Tanaka Hisashi, Giuliano Armando E
Impact of Grade on Survival in Pleomorphic Xanthoastrocytoma and Low Prevalence of BRAF V600E Mutation.
World neurosurgery | 2022-08-01 | PMID 35618235
Gandham Edmond Jonathan, Goyal-Honavar Abhijit, Beno Daniel and 7 more
Mouse models of Alzheimer's disease for preclinical research.
Neurochemistry international | 2022-09-01 | PMID 35618239
Watamura Naoto, Sato Kaori, Saido Takaomi C
An emerging phenotype of pulmonary arterial hypertension patients carrying SOX17 variants.
The European respiratory journal | 2022-12-01 | PMID 35618278
Montani David, Lechartier Benoit, Girerd Barbara and 19 more
Bufalin stimulates antitumor immune response by driving tumor-infiltrating macrophage toward M1 phenotype in hepatocellular carcinoma.
Journal for immunotherapy of cancer | 2022-05-01 | PMID 35618286
Yu Zhuo, Li Yuyao, Li Yue and 13 more
Real-life experience of ledipasvir and sofosbuvir for HCV infected Korean patients: a multicenter cohort study.
The Korean journal of internal medicine | 2022-11-01 | PMID 35618302
Lee Soon Kyu, Lee Sung Won, Lee Hae Lim and 19 more
Senescence-induced endothelial phenotypes underpin immune-mediated senescence surveillance.
Genes & development | 2022-05-01 | PMID 35618311
Yin Kelvin, Patten Daniel, Gough Sarah and 14 more
Metabolic interactions shape a community's phenotype.
Trends in microbiology | 2022-07-01 | PMID 35618541
Melkonian Chrats, Seidl Michael F, van der Hooft Justin J J and 1 more
Cellular and molecular mechanisms of plasticity in cancer.
Trends in cancer | 2022-09-01 | PMID 35618573
Torborg Stefan R, Li Zhuxuan, Chan Jason E and 1 more
Changes of immune-related factors in the blood of schizophrenia and bipolar disorder patients receiving monotherapy.
Translational psychiatry | 2022-05-26 | PMID 35618730
Duan Fangyuan, Zhao Shunan, Xia Cuihua and 14 more
Plant phenotype relationship corpus for biomedical relationships between plants and phenotypes.
Scientific data | 2022-05-26 | PMID 35618736
Cho Hyejin, Kim Baeksoo, Choi Wonjun and 2 more
A Mild Case of Autosomal Recessive Osteopetrosis Masquerading as the Dominant Form Involving Homozygous Deep Intronic Variations in the CLCN7 Gene.
Calcified tissue international | 2022-10-01 | PMID 35618777
Hofstaetter Jochen G, Atkins Gerald J, Kato Hajime and 9 more
Achievements, prospects and challenges in precision care for monogenic insulin-deficient and insulin-resistant diabetes.
Diabetologia | 2022-11-01 | PMID 35618782
Bonnefond Amélie, Semple Robert K
Human enterococcal isolates as reservoirs for macrolide-lincosamide-streptogramin and other resistance genes.
The Journal of antibiotics | 2022-07-01 | PMID 35618783
Mišić Milena, Kocić Branislava, Arsović Aleksandra and 4 more
Different DNA methylome, transcriptome and histological features in uterine fibroids with and without MED12 mutations.
Scientific reports | 2022-05-26 | PMID 35618793
Maekawa Ryo, Sato Shun, Tamehisa Tetsuro and 4 more
Autoreactive CD8+ T cells are restrained by an exhaustion-like program that is maintained by LAG3.
Nature immunology | 2022-06-01 | PMID 35618829
Grebinoski Stephanie, Zhang Qianxia, Cillo Anthony R and 12 more
Immune disease risk variants regulate gene expression dynamics during CD4+ T cell activation.
Nature genetics | 2022-06-01 | PMID 35618845
Soskic Blagoje, Cano-Gamez Kiki, Smyth Deborah J and 14 more
Genes: CD4
Multiomics reveals persistence of obesity-associated immune cell phenotypes in adipose tissue during weight loss and weight regain in mice.
Nature communications | 2022-05-26 | PMID 35618862
Cottam Matthew A, Caslin Heather L, Winn Nathan C and 1 more
Proteomic phenotype of cerebral organoids derived from autism spectrum disorder patients reveal disrupted energy metabolism, cellular components, and biological processes.
Molecular psychiatry | 2022-09-01 | PMID 35618886
Ilieva Mirolyuba, Aldana Blanca Irene, Vinten Kasper Tore and 5 more
Assessing the contribution of genetic nurture to refractive error.
European journal of human genetics : EJHG | 2022-11-01 | PMID 35618892
Guggenheim Jeremy A, Clark Rosie, Zayats Tetyana and 1 more
Tocopherol Accumulation and Temporal Expression Analysis of VTE1 and VTE5 Gene Family in Fruit of Two Contrasting Avocado Genotypes.
Plant foods for human nutrition (Dordrecht, Netherlands) | 2022-06-01 | PMID 35618894
Valdez-Agramón Rosalva C, Valdez-Morales Maribel, López-Meyer Melina and 2 more
Mapping and identification of QTL in 5601T × U99-310255 RIL population using SNP genotyping: soybean seed quality traits.
Molecular biology reports | 2022-07-01 | PMID 35618938
Cunicelli Mia, Olukolu Bode A, Sams Carl and 3 more
Successful restoration of archived ovine formalin fixed paraffin-embedded tissue DNA and single nucleotide polymorphism analysis.
Veterinary research communications | 2023-01-01 | PMID 35618986
Kravitz Amanda, Tyler Ron, Manohar B Murali and 3 more
Generation of Markerless Gene Deletion Mutants in Listeria monocytogenes Using a Mutated pheS for Counterselection.
Methods in molecular biology (Clifton, N.J.) | 2022-01-01 | PMID 35619020
Ran Sapir Shai, Boichis Etai, Herskovits Anat A
Copula miss-specification in REML multivariate genetic animal model estimation.
Genetics, selection, evolution : GSE | 2022-05-26 | PMID 35619063
Rohmer Tom, Ricard Anne, David Ingrid
Role of human organic cation transporter-1 (OCT-1/SLC22A1) in modulating the response to metformin in patients with type 2 diabetes.
BMC endocrine disorders | 2022-05-26 | PMID 35619086
Kawoosa Fizalah, Shah Zafar A, Masoodi Shariq R and 6 more
Discovery of new therapeutic targets in ovarian cancer through identifying significantly non-mutated genes.
Journal of translational medicine | 2022-05-26 | PMID 35619151
Al-Farsi Halema, Al-Azwani Iman, Malek Joel A and 3 more
MTHFR Polymorphisms and Cardiac Parameters in Patients with Diabetic Retinopathy.
Current diabetes reviews | 2023-01-01 | PMID 35619268
Alcântara João Otávio Scarano, de Assis Caroline Severo, Diniz Tainá Gomes and 9 more
Alz-Disc: A Tool to Discriminate Disease-causing and Neutral Mutations in Alzheimer's Disease.
Combinatorial chemistry & high throughput screening | 2023-01-01 | PMID 35619290
Kulandaisamy A, Parvathy Dharshini S Akila, Gromiha M Michael
Melatonin and andrographolide synergize to inhibit the colospheroid phenotype by targeting Wnt/beta-catenin signaling.
Journal of pineal research | 2022-08-01 | PMID 35619550
Sokolov Daniil, Sharda Neha, Giri Banabihari and 10 more
The Effect of Peripheral Immune Cell Counts on the Risk of Multiple Sclerosis: A Mendelian Randomization Study.
Frontiers in immunology | 2022-01-01 | PMID 35619713
He Di, Liu Liyang, Shen Dongchao and 2 more
Complement Factor I Variants in Complement-Mediated Renal Diseases.
Frontiers in immunology | 2022-01-01 | PMID 35619721
Zhang Yuzhou, Goodfellow Renee X, Ghiringhelli Borsa Nicolo and 10 more
Scrutinizing Deleterious Nonsynonymous SNPs and Their Effect on Human POLD1 Gene.
Genetics research | 2022-01-01 | PMID 35620275
Bappy Md Nazmul Islam, Roy Anindita, Rabbi Md Gulam Rabbany and 7 more
Contribution of a genetic risk score to ethnic differences in fatty liver disease.
Liver international : official journal of the International Association for the Study of the Liver | 2022-10-01 | PMID 35620859
Kubiliun Maddie J, Cohen Jonathan C, Hobbs Helen H and 1 more
Genes: GCKR, HSD17B13, MBOAT7, PNPLA3, TM6SF2, TMC4
Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago.
Molecular genetics & genomic medicine | 2022-08-01 | PMID 35620871
Sbalchiero Anna, Abu Hweij Yasmin, Mazza Tommaso and 7 more
The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype.
Pediatric endocrinology, diabetes, and metabolism | 2022-01-01 | PMID 35620925
Wesół-Kucharska Dorota, Rokicki Dariusz, Greczan Milena and 7 more
Discovery of the novel HLA-C*08:03:05 allele in a Taiwanese individual.
HLA | 2022-10-01 | PMID 35620939
Yang Kuo-Liang, Li Chi-Cheng, Lin Py-Yu
Identification of the novel HLA-C*06:318 allele by next-generation sequencing in a Chinese individual.
HLA | 2022-10-01 | PMID 35620967
Dong Lina, Fu Rui, Wang Fang and 2 more
Characterization of the novel HLA-C*07:1001N allele by next-generation sequencing.
HLA | 2022-10-01 | PMID 35620970
Gatouillat Grégory, Tonye-Libyh Marcelle, Tabary Thierry and 2 more
The novel HLA-DRB1*12:01:10 allele was identified by next-generation sequencing.
HLA | 2022-10-01 | PMID 35620973
Chen Nanying, Zhang Wei, Xu Xianguo and 2 more
Benchmarking of univariate pleiotropy detection methods applied to epilepsy.
Human mutation | 2022-09-01 | PMID 35620985
Adesoji Oluyomi M, Schulz Herbert, May Patrick and 3 more
The significance of the fusion partner gene genomic neighborhood analysis in translocation-defined tumors.
Molecular genetics & genomic medicine | 2022-08-01 | PMID 35621010
Mosaieby Elaheh, Martínek Petr, Ondič Ondrej
Non-small cell lung cancer with EGFR exon 20 insertion mutation: a systematic literature review and meta-analysis of patient outcomes.
Current medical research and opinion | 2022-08-01 | PMID 35621011
Kwon Christina Soeun, Lin Huamao M, Crossland Victoria and 5 more
Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis.
Journal of cellular physiology | 2022-06-01 | PMID 35621037
Qiu Yi-Ling, Wang Li, Huang Min and 10 more
A potential early clinical phenotype of necrotizing meningoencephalitis in genetically at-risk pug dogs.
Journal of veterinary internal medicine | 2022-07-01 | PMID 35621070
Windsor Rebecca, Stewart Samuel, Schmidt Jessica and 7 more
Victorian evolution of inherited retinal diseases natural history registry (VENTURE study): Rationale, methodology and initial participant characteristics.
Clinical & experimental ophthalmology | 2022-09-01 | PMID 35621151
Britten-Jones Alexis Ceecee, O'Hare Fleur, Edwards Thomas L and 1 more
A gain-of-function mutation in the ITPR1 gating domain causes male infertility in mice.
Journal of cellular physiology | 2022-08-01 | PMID 35621185
Sun Bo, Ni Mingke, Tian Shanshan and 13 more
Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol.
Journal of the American Heart Association | 2022-06-07 | PMID 35621206
Shi Mingjian, Wang Chuan, Mei Hao and 12 more
Genes: DHTKD1, MSR1, NDUFS4
Interleukin-1β activated c-FOS transcription factor binds preferentially to a specific allele of the matrix metalloproteinase-13 promoter and increases susceptibility to endometriosis.
Journal of cellular physiology | 2022-07-01 | PMID 35621221
Pandit Anuradha, Das Mahapatra Pramathes, Saha Priyanka and 2 more
A homozygous splice variant in ATP5PO, disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families.
Journal of inherited metabolic disease | 2022-09-01 | PMID 35621276
Ganapathi Mythily, Friocourt Gaelle, Gueguen Naig and 36 more
A homozygous exonic variant leading to exon skipping in ABCC8 as the cause of severe congenital hyperinsulinism.
American journal of medical genetics. Part A | 2022-08-01 | PMID 35621279
Reyes Diaz Jacqueline V, Jin Yulin, Garber Kathryn and 5 more
Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype.
Journal of cellular physiology | 2022-08-01 | PMID 35621301
Kiseleva Ekaterina, Serbina Olesya, Karpukhina Anna and 2 more
Managing Uncertainty for and With Family: Communication Strategies and Motivations in Familial Uncertainty Management for Hereditary Cancer.
Qualitative health research | 2022-07-01 | PMID 35621326
Campbell-Salome Gemme, Barbour Joshua B
God playing dice, revisited: determinism and indeterminism in studies of stochastic phenotypic variation.
Emerging topics in life sciences | 2022-09-09 | PMID 35621351
Lajus Dmitry
Host genomic influence on bacterial composition in the switchgrass rhizosphere.
Molecular ecology | 2022-07-01 | PMID 35621390
Sutherland Jeremy, Bell Terrence, Trexler Ryan V and 2 more
PIK3CA Mutation as Potential Poor Prognostic Marker in Asian Female Breast Cancer Patients Who Received Adjuvant Chemotherapy.
Current oncology (Toronto, Ont.) | 2022-04-19 | PMID 35621626
Cho Yoon Ah, Ko Seung Yeon, Suh Yong Joon and 9 more
Progressing Vulvar Melanoma Caused by Instability in cKIT Juxtamembrane Domain: A Case Report and Review of Literature.
Current oncology (Toronto, Ont.) | 2022-04-29 | PMID 35621644
Englert-Golon Monika, Budny Bartłomiej, Lewandowska Małgorzata and 7 more
Method for the Intraoperative Detection of IDH Mutation in Gliomas with Differential Mobility Spectrometry.
Current oncology (Toronto, Ont.) | 2022-05-04 | PMID 35621655
Haapala Ilkka, Kondratev Anton, Roine Antti and 10 more
Efficacy of Osimertinib in Lung Squamous Cell Carcinoma Patients with EGFR Gene Mutation-Case Report and a Literature Review.
Current oncology (Toronto, Ont.) | 2022-05-13 | PMID 35621675
Rekowska Anna, Rola Piotr, Wójcik-Superczyńska Magdalena and 3 more
Mutation Profiles of Ovarian Seromucinous Borderline Tumors in Japanese Patients.
Current oncology (Toronto, Ont.) | 2022-05-18 | PMID 35621684
Sasamori Hiroki, Nakayama Kentaro, Razia Sultana and 9 more
HRAS Q61L Mutation as a Possible Target for Non-Small Cell Lung Cancer: Case Series and Review of Literature.
Current oncology (Toronto, Ont.) | 2022-05-20 | PMID 35621690
Mathiot Laurent, Herbreteau Guillaume, Robin Siméon and 5 more
Association of HLA-DQ Heterodimer Residues -18β and β57 With Progression From Islet Autoimmunity to Diabetes in the Diabetes Prevention Trial-Type 1.
Diabetes care | 2022-07-07 | PMID 35621697
Zhao Lue Ping, Skyler Jay, Papadopoulos George K and 9 more
Generation and analysis of pseudohypoaldosteronism type II knock-in mice caused by a nonsense KLHL3 mutation in the Kelch domain.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2022-06-01 | PMID 35621709
Lin Chien-Ming, Sung Chih-Chien, Yang Sung-Sen and 3 more
Nucleophosmin 1: from its pathogenic role to a tantalizing therapeutic target in acute myeloid leukemia.
Hematology (Amsterdam, Netherlands) | 2022-12-01 | PMID 35621728
Shi Yuye, Xue Yuhao, Wang Chunling and 1 more
Causal Graph Among Serum Lipids and Glycemic Traits: A Mendelian Randomization Study.
Diabetes | 2022-08-01 | PMID 35622003
Zhu Ziwei, Wang Kai, Hao Xingjie and 3 more
ARTP and NTG compound mutations improved Cry protein production and virulence of Bacillus thuringiensis X023.
Applied microbiology and biotechnology | 2022-06-01 | PMID 35622123
Zhu Zirong, Chen Wenhui, Zhou Hongbo and 6 more
In vivo impact of JAK3 A573V mutation revealed using zebrafish.
Cellular and molecular life sciences : CMLS | 2022-05-27 | PMID 35622134
Basheer Faiza, Bulleeraz Vilasha, Ngo Viet Q T and 2 more
NOTCH gene alterations in metastatic colorectal cancer in the Nationwide Cancer Genome Screening Project in Japan (SCRUM-Japan GI-SCREEN).
Journal of cancer research and clinical oncology | 2022-10-01 | PMID 35622165
Kajiwara Takeshi, Nishina Tomohiro, Nakasya Akio and 27 more
Phenotypic plasticity of acoustic traits in high-frequency lebinthine crickets (Orthoptera: Eneopterinae: Lebinthina).
Die Naturwissenschaften | 2022-05-27 | PMID 35622169
Ballesteros Alberto Rodríguez, Tan Ming Kai, Robillard Tony
Comparative analysis of cancer gene mutations using targeted sequencing in matched primary and recurrent gastric cancers after chemotherapy.
Genes & genomics | 2022-11-01 | PMID 35622232
Huh Yeon-Ju, Cho Sung-Yup, Cho Min-Sun and 2 more
Genetically predicted physical activity is associated with lower serum urate concentrations.
Genes & genomics | 2022-07-01 | PMID 35622233
Guan Ying, Wei Jiahe, Meng Lifeng and 4 more
Circulating interleukin-37 declines with aging in healthy humans: relations to healthspan indicators and IL37 gene SNPs.
GeroScience | 2023-02-01 | PMID 35622271
Brunt Vienna E, Ikoba Akpevweoghene P, Ziemba Brian P and 5 more
Exploring and mitigating potential bias when genetic instrumental variables are associated with multiple non-exposure traits in Mendelian randomization.
European journal of epidemiology | 2022-07-01 | PMID 35622304
Yang Qian, Sanderson Eleanor, Tilling Kate and 2 more
The novel histone deacetylase inhibitor pracinostat suppresses the malignant phenotype in human glioma.
Molecular biology reports | 2022-08-01 | PMID 35622308
Chen Mantao, Zhang Luyuan, Zhan Renya and 1 more
NGS-Based B-Cell Receptor Repertoire AnalysisRepertoire analyses in the Context of Inborn Errors of Immunity.
Methods in molecular biology (Clifton, N.J.) | 2022-01-01 | PMID 35622327
van Schouwenburg Pauline A, van der Burg Mirjam, IJspeert Hanna
Type 2 Diabetes, Fasting Glucose, Hemoglobin A1c Levels and Risk of Primary Open-Angle Glaucoma: A Mendelian Randomization Study.
Investigative ophthalmology & visual science | 2022-05-02 | PMID 35622353
Hu Zhao, Zhou Feixiang, Kaminga Atipatsa Chiwanda and 1 more
Association analysis between reproduction genes INHA, PGR, RARG with lamb and other traits of Liaoning cashmere goats.
Animal biotechnology | 2023-12-01 | PMID 35622393
Chen Rui, Liu Jichang, Zhang Yurou and 13 more
Nonsynonymous SNPs within C7H15orf39 and NOS2 are associated with boar semen quality.
Animal biotechnology | 2023-12-01 | PMID 35622405
Wang Tiansu, Feng Yue, Chen Dake and 7 more
Insertion/deletion (Indel) variant of the goat RORA gene is associated with growth traits.
Animal biotechnology | 2023-12-01 | PMID 35622416
Zhou Qian, Hu Huina, Yang Yuta and 5 more
High Nasal Nitric Oxide, Cilia Analyses, and Genotypes in a Retrospective Cohort of Children with Primary Ciliary Dyskinesia.
Annals of the American Thoracic Society | 2022-10-01 | PMID 35622418
Legendre Marie, Thouvenin Guillaume, Taytard Jessica and 8 more