×
Close
Sign Up
Login
Home
SCI Abstract
Library D
Community
Events
Events & Partner
WeMed
Media Partners
Educational Partner
User Tools
FAQ/USER GUIDE
Language
English
中文/ Chinese
Contact Us
×
Close
mdla_1
mdla_2
mdla_3
mdla_4
mdla_5
mdla_6
Categories
Genetics & Heredity
13905
Global Medical University
4809
Allergy
1437
Anatomy & Morphology
1329
Andrology
284
Anesthesia & Intensive Care
1210
Anesthesiology
5017
Audiology & Speech-Language Pathology
254
Behavioral Sciences
90
Biochemical Research Methods
6592
Biochemistry & Molecular Biology
27844
Biodiversity Conservation
290
Biology
7813
Biophysics
7790
Biotechnology & Applied Microbiology
7729
Cardiac & Cardiovascular Systems
29067
Cardiovascular & Respiratory Systems
1178
Cell & Tissue Engineering
665
Cell Biology
10099
Chemistry, Analytical
3638
Chemistry, Applied
10348
Chemistry, Medicinal
8150
Chemistry, Multidisciplinary
16937
Clinical Immunology & Infectious Disease
374
Clinical Medicine
7335
Clinical Neurology
15360
Clinical Psychology & Psychiatry
1209
Critical Care Medicine
2993
Dentistry, Oral Surgery & Medicine
12025
Dermatology
6166
Developmental Biology
6393
Ecology
566
Education, Scientific Disciplines
1854
Emergency Medicine
3719
Endocrinology, Metabolism & Nutrition
22457
Engineering, Biomedical
3526
Entomology
459
Environmental Medicine & Public Health
4316
Evolutionary Biology
245
Gastroenterology & Hepatology
11057
General & Internal Medicine
6453
Geriatrics & Gerontology
4593
Gerontology
353
Health Care Sciences & Services
14744
Health Policy & Services
539
Hematology
4930
Immunology
23204
Infectious Diseases
12808
Integrative & Complementary Medicine
2813
Medical Ethics
1147
Medical Informatics
2130
Medical Laboratory Technology
360
Medicine, General & Internal
41358
Medicine, Legal
481
Medicine, Research & Experimental
16194
Microbiology
21797
Mycology
0
Nanoscience & Nanotechnology
4712
Neuroimaging
1259
Neurology
4011
Neurosciences
37395
Nursing
8436
Nutrition & Dietetics
7251
Obstetrics & Gynecology
7520
Oncology
48071
Ophthalmology
9041
Optics
3872
Orthopedics
10630
Orthopedics, Rehabilitation & Sports Medicine
1641
Otolaryngology
1382
Otorhinolaryngology
4387
Parasitology
1087
Pathology
4496
Pediatrics
19866
Peripheral Vascular Disease
4431
Pharmacology & Pharmacy
32350
Pharmacology/Toxicology
11430
Physiology
8166
Polymer Science
490
Primary Health Care
768
Psychiatry
17774
Psychology
4750
Psychology, Applied
101
Psychology, Biological
335
Psychology, Clinical
751
Psychology, Developmental
244
Psychology, Educational
139
Psychology, Experimental
147
Psychology, Mathematical
0
Psychology, Multidisciplinary
1598
Psychology, Psychoanalysis
26
Psychology, Social
108
Public Health & Health Care Science
2015
Public, Environmental & Occupational Health
25462
Quantum Science & Technology
0
Radiology, Nuclear Medicine & Imaging
11630
Radiology, Nuclear Medicine & Medical Imaging
7192
Rehabilitation
2621
Remote Sensing
0
Reproductive Biology
2686
Reproductive Medicine
1117
Research/Laboratory Medicine & Medical Technology
3717
Respiratory System
6569
Rheumatology
5321
Social Sciences, Biomedical
1065
Substance Abuse
2485
Surgery
31811
Toxicology
3981
Transplantation
788
Tropical Medicine
271
Urology & Nephrology
11780
Veterinary Sciences
27
Virology
2129
Zoology
0
Channels
FRONTIERS IN GENETICS
5107
Genetics
5
NEJM Genetics
2
Medrxiv - Genetic And Genomic Medicine
1665
CANCER GENE THERAPY
355
CHROMOSOMA
84
CLINICAL GENETICS
79
CURRENT GENETICS
127
CURRENT OPINION IN GENETICS & DEVELOPMENT
261
EPIGENETICS & CHROMATIN
121
EPIGENOMICS
18
EPILEPSIA
136
GENE THERAPY
167
GENETICS IN MEDICINE
50
GENOME MEDICINE
280
GENOMICS PROTEOMICS & BIOINFORMATICS
190
HUMAN GENETICS
334
HUMAN MUTATION
82
JOURNAL OF HUMAN GENETICS
269
JOURNAL OF MEDICAL GENETICS
367
NATURE REVIEWS GENETICS
302
NPJ GENOMIC MEDICINE
167
ORPHANET JOURNAL OF RARE DISEASES
753
ANNALS OF HUMAN GENETICS
18
CYTOGENETIC AND GENOME RESEARCH
89
G3-GENES GENOMES GENETICS
19
GENETIC EPIDEMIOLOGY
13
HUMAN GENOMICS
212
HUMAN HEREDITY
30
INTERNATIONAL JOURNAL OF IMMUNOGENETICS
15
JOURNAL OF EVOLUTIONARY BIOLOGY
77
JOURNAL OF GENETIC COUNSELING
92
PSYCHIATRIC GENETICS
104
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
259
FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES
17
GENETICS AND MOLECULAR RESEARCH
10
GLOBAL MEDICAL GENETICS
137
INTERNATIONAL JOURNAL OF NEONATAL SCREENING
68
JOURNAL OF COMMUNITY GENETICS
167
NON-CODING RNA
114
FUNCTIONAL & INTEGRATIVE GENOMICS
491
GENETICA
114
IMMUNOGENETICS
140
JOURNAL OF APPLIED GENETICS
222
JOURNAL OF GENETICS
191
RUSSIAN JOURNAL OF GENETICS
385
SCI Abstract
search
ALL
RECOMMENDED
+
BRMDA: prediction model for potential microbe-drug associations based on bilinear attention networks and random forest
IntroductionUncharted microbe-drug relationships constitute an under-exploited reservoir of therapeutic leads. In this man...
Frontiers In Genetics
comment
0
thumb_up
0
Correction: A systematic exploration of gut microbiota–driven blood metabolites in sepsis: an integrated bioinformatics and genetic association study
Incorrect funding.The funder Chongqing Natural Science Foundation, CSTB2024NSCQ-KJFZMSX0101 to Peng Zhu was erroneously om...
Frontiers In Genetics
comment
0
thumb_up
0
Pan-transcriptome analysis of pine wilt disease-resistant and susceptible Pinus species and a hybrid
Pine trees, globally distributed and economically vital evergreen conifers, are threatened by pine wilt disease (PWD) attr...
Frontiers In Genetics
comment
0
thumb_up
0
Case Report: Novel pathogenic variant in autosomal recessive WNT10A-related odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia (OODD) is a rare, autosomal recessive disorder caused by pathogenic variants in the WNT10A ...
Frontiers In Genetics
comment
0
thumb_up
0
Advances in algorithms for normalizer gene selection in qRT-PCR: implications for cancer biology and precision medicine
Quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR) plays a significant role in gene expression analysi...
Frontiers In Genetics
comment
0
thumb_up
0
Tumor microenvironment-induced epigenetic reprogramming of Tregs and its impact on immunotherapy
The tumor microenvironment (TME) represents a complex system comprising various cells and extracellular matrix components ...
Frontiers In Genetics
comment
0
thumb_up
0
Developmental and epileptic encephalopathies with germline PIGA variants in five Chinese children: a case report and literature review
BackgroundDiseases associated with the germline PIGA gene include multiple congenital anomalies-hypotonia-seizures syndrom...
Frontiers In Genetics
comment
0
thumb_up
0
Pharmacist workforce training in pharmacogenomics with a focus on rural and underserved areas
ObjectiveOur primary objective is to demonstrate the benefits of pharmacogenomic (PGx) education for pharmacists that serv...
Frontiers In Genetics
comment
0
thumb_up
0
Expanding the clinical and mutational spectrum of hereditary spastic paraplegia type 4 in a cohort of patients from central China
BackgroundMutations in the SPAST gene cause autosomal dominant hereditary spastic paraplegia (HSP) type 4 (SPG4), which is...
Frontiers In Genetics
comment
0
thumb_up
0
Raloxifene ameliorates cartilage and subchondral bone microstructural degeneration in the ovariectomy-induced spontaneous postmenopausal osteoarthritis
The prevalence and incidence of osteoarthritis (OA) increase significantly in women after menopause, indicating an importa...
Frontiers In Genetics
comment
0
thumb_up
0
Case Report: Prenatal genetic analysis of a rare fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) karyotype
ObjectiveTo perform a genetic analysis of a rare complex chimeric fetus with a 45,X/46,X,dic r(Y; Y)/46,X,r(Y) karyotype, ...
Frontiers In Genetics
comment
0
thumb_up
0
Renpenning syndrome caused by the c.459_462delAGAG mutation in PQBP1: a case report and literature review
BackgroundRenpenning syndrome (OMIM: 309500) is a rare X-linked intellectual disability caused by variations in the polygl...
Frontiers In Genetics
comment
0
thumb_up
0
A graph clustering algorithm with hypergraph learning and a core-attachment strategy for protein complex identification
Protein complexes play a crucial role in cellular biological processes. Identifying these complexes is essential for under...
Frontiers In Genetics
comment
0
thumb_up
0
Editorial: Advances in molecular genetics of Marfan syndrome and related disorders
Marfan syndrome (MFS, OMIM#154700) is a rare heritable multisystem connective tissue disorder 9 (HCTD) with an estimated i...
Frontiers In Genetics
comment
0
thumb_up
0
Genomic and transcriptomic insights into aflatoxin-induced intrahepatic cholangiocarcinoma: an integrated pathway and meta-analysis study
IntroductionEnvironmental and chemical exposures are major yet incompletely characterized drivers of human carcinogenesis....
Frontiers In Genetics
comment
0
thumb_up
0
A single-cell multi-omics atlas of human eyelid skin
Human skin acts as a primary protective organ against the external environment. It plays key physiological roles, includin...
Frontiers In Genetics
comment
0
thumb_up
0
Genetic association of LOC100130476 rs80213143 with susceptibility and renal involvement in systemic lupus erythematosus
BackgroundsSystemic lupus erythematosus (SLE) is an autoimmune disease with multi-organ involvement, and lupus nephritis (...
Frontiers In Genetics
comment
0
thumb_up
0
Serum tumor markers combined with HRCT for malignancy risk assessment of solitary pulmonary nodules: a retrospective study
IntroductionThis study aims to investigate the correlation between serum tumor markers (CEA, NSE, CA-125, and CYFRA 21-1) ...
Frontiers In Genetics
comment
0
thumb_up
0
Federated, governed, and interoperable? The emerging architecture of public human genomic data infrastructures: a European perspective
Public infrastructures for human genomic data are increasingly incorporating federated approaches alongside centralized an...
Frontiers In Genetics
comment
0
thumb_up
0
TTN variants in pediatric cardiomyopathy: a retrospective cohort study
BackgroundTitin (TTN) variants have been implicated in various types of cardiomyopathy. Allelic variant heterogeneity resu...
Frontiers In Genetics
comment
0
thumb_up
0
Novel variant alters splicing of TGFB2 in family with features of Loeys-Dietz syndrome
1 IntroductionLoeys-Dietz syndrome (LDS) is a rare connective tissue disorder with a prevalence of 1 in 100,000 individual...
Frontiers In Genetics
comment
0
thumb_up
0
SiMul-db: a database of single and multi-target Cas9 guides for hazelnut editing
Hazelnuts are trees belonging to the Betulaceae family and Corylus genus (Wani et al., 2020). Due to their delicious flavo...
Frontiers In Genetics
comment
0
thumb_up
0
Localization is the key to action: regulatory peculiarities of lncRNAs
To understand the transcriptomic profile of an individual cell in a multicellular organism, we must comprehend its surroun...
Frontiers In Genetics
comment
0
thumb_up
0
Identification and validation the predictive biomarkers based on risk-adjusted control chart in gemcitabine with or without erlotinib for pancreatic cancer therapy
1 IntroductionPancreatic ductal adenocarcinoma (PDAC) is a common gastrointestinal malignancy with a 5-year survival rate ...
Frontiers In Genetics
comment
0
thumb_up
0
Genome-wide identification and expression analysis of the PsKIN gene family in pea
1 IntroductionPeas (Pisum sativum L.) are integral to the global agricultural and nutritional sectors. Despite their impor...
Frontiers In Genetics
comment
0
thumb_up
0
The risk status, signatures of adaptation, and environmental suitability of village-based indigenous chickens from certain regions of Limpopo and KwaZulu-Natal provinces of South Africa
IntroductionIn South Africa, as in most developing countries, indigenous chickens contribute significantly to the liveliho...
Frontiers In Genetics
comment
0
thumb_up
0
Assessing the causal relationships between circulating metabolic biomarkers and breast cancer by using mendelian randomization
1 IntroductionBreast cancer (BC) remains the most common cancer among women globally. In 2024, the United States is expect...
Frontiers In Genetics
comment
0
thumb_up
0
Identification of hub programmed cell death-related genes and immune infiltration in Crohn’s disease using bioinformatics
1 IntroductionCrohn’s disease (CD) is an inflammatory bowel disease affecting any part of the gastrointestinal tract (Peta...
Frontiers In Genetics
comment
0
thumb_up
0
Identification of selective sweep and associated QTL traits in Iranian Ovis aries and Ovis orientalis populations
1 IntroductionAnimal domestication has significantly influenced human life. Due to their high adaptability to various clim...
Frontiers In Genetics
comment
0
thumb_up
0
Genome-wide identification and expression analysis of the BAHD gene family in Leonurus japonicus
1 IntroductionSecondary metabolites endowed with specialized bioactivity are integral to the growth and developmental proc...
Frontiers In Genetics
comment
0
thumb_up
0
Load More
Modal title
×
Modal title
×
Share
Login
Global News and Health Forum
Join Now!
Member Login
Remember me
Forgot password?
Or using
Linkedin