×
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
14013
Global Medical University
4812
Allergy
1434
Anatomy & Morphology
1342
Andrology
293
Anesthesia & Intensive Care
1218
Anesthesiology
5074
Audiology & Speech-Language Pathology
259
Behavioral Sciences
91
Biochemical Research Methods
6597
Biochemistry & Molecular Biology
28084
Biodiversity Conservation
292
Biology
7842
Biophysics
7836
Biotechnology & Applied Microbiology
7768
Cardiac & Cardiovascular Systems
29277
Cardiovascular & Respiratory Systems
1203
Cell & Tissue Engineering
669
Cell Biology
10197
Chemistry, Analytical
3672
Chemistry, Applied
10412
Chemistry, Medicinal
8192
Chemistry, Multidisciplinary
17116
Clinical Immunology & Infectious Disease
377
Clinical Medicine
7475
Clinical Neurology
15441
Clinical Psychology & Psychiatry
1211
Critical Care Medicine
2996
Dentistry, Oral Surgery & Medicine
12145
Dermatology
6307
Developmental Biology
6468
Ecology
576
Education, Scientific Disciplines
1866
Emergency Medicine
3766
Endocrinology, Metabolism & Nutrition
22527
Engineering, Biomedical
3530
Entomology
460
Environmental Medicine & Public Health
4378
Evolutionary Biology
246
Gastroenterology & Hepatology
11114
General & Internal Medicine
6498
Geriatrics & Gerontology
4569
Gerontology
341
Health Care Sciences & Services
14874
Health Policy & Services
545
Hematology
4955
Immunology
23372
Infectious Diseases
12926
Integrative & Complementary Medicine
2802
Medical Ethics
1157
Medical Informatics
2142
Medical Laboratory Technology
361
Medicine, General & Internal
41694
Medicine, Legal
481
Medicine, Research & Experimental
16347
Microbiology
21917
Mycology
0
Nanoscience & Nanotechnology
4718
Neuroimaging
1266
Neurology
4044
Neurosciences
37546
Nursing
8548
Nutrition & Dietetics
7338
Obstetrics & Gynecology
7580
Oncology
48488
Ophthalmology
9073
Optics
3868
Orthopedics
10695
Orthopedics, Rehabilitation & Sports Medicine
1660
Otolaryngology
1393
Otorhinolaryngology
4430
Parasitology
1090
Pathology
4542
Pediatrics
20012
Peripheral Vascular Disease
4415
Pharmacology & Pharmacy
32509
Pharmacology/Toxicology
11458
Physiology
8203
Polymer Science
500
Primary Health Care
787
Psychiatry
17911
Psychology
4760
Psychology, Applied
101
Psychology, Biological
336
Psychology, Clinical
746
Psychology, Developmental
244
Psychology, Educational
139
Psychology, Experimental
147
Psychology, Mathematical
0
Psychology, Multidisciplinary
1577
Psychology, Psychoanalysis
28
Psychology, Social
109
Public Health & Health Care Science
2034
Public, Environmental & Occupational Health
25711
Quantum Science & Technology
0
Radiology, Nuclear Medicine & Imaging
11702
Radiology, Nuclear Medicine & Medical Imaging
7283
Rehabilitation
2683
Remote Sensing
0
Reproductive Biology
2695
Reproductive Medicine
1119
Research/Laboratory Medicine & Medical Technology
3745
Respiratory System
6623
Rheumatology
5368
Social Sciences, Biomedical
1076
Substance Abuse
2500
Surgery
31943
Toxicology
4004
Transplantation
818
Tropical Medicine
278
Urology & Nephrology
11826
Veterinary Sciences
28
Virology
2148
Zoology
0
Channels
JOURNAL OF GENETICS
193
Genetics
5
NEJM Genetics
2
Medrxiv - Genetic And Genomic Medicine
1681
CANCER GENE THERAPY
357
CHROMOSOMA
84
CLINICAL GENETICS
86
CURRENT GENETICS
120
CURRENT OPINION IN GENETICS & DEVELOPMENT
245
EPIGENETICS & CHROMATIN
122
EPIGENOMICS
19
EPILEPSIA
144
FRONTIERS IN GENETICS
5142
GENE THERAPY
159
GENETICS IN MEDICINE
55
GENOME MEDICINE
282
GENOMICS PROTEOMICS & BIOINFORMATICS
192
HUMAN GENETICS
338
HUMAN MUTATION
84
JOURNAL OF HUMAN GENETICS
269
JOURNAL OF MEDICAL GENETICS
374
NATURE REVIEWS GENETICS
310
NPJ GENOMIC MEDICINE
167
ORPHANET JOURNAL OF RARE DISEASES
759
ANNALS OF HUMAN GENETICS
18
CYTOGENETIC AND GENOME RESEARCH
90
G3-GENES GENOMES GENETICS
19
GENETIC EPIDEMIOLOGY
13
HUMAN GENOMICS
213
HUMAN HEREDITY
30
INTERNATIONAL JOURNAL OF IMMUNOGENETICS
16
JOURNAL OF EVOLUTIONARY BIOLOGY
77
JOURNAL OF GENETIC COUNSELING
98
PSYCHIATRIC GENETICS
108
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
260
FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES
17
GENETICS AND MOLECULAR RESEARCH
10
GLOBAL MEDICAL GENETICS
138
INTERNATIONAL JOURNAL OF NEONATAL SCREENING
70
JOURNAL OF COMMUNITY GENETICS
168
NON-CODING RNA
116
FUNCTIONAL & INTEGRATIVE GENOMICS
491
GENETICA
114
IMMUNOGENETICS
140
JOURNAL OF APPLIED GENETICS
222
RUSSIAN JOURNAL OF GENETICS
396
SCI Abstract
search
ALL
RECOMMENDED
+
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent variant [c.589G>A, p.(Ala197Thr)] in the Pakistani population
Primary microcephaly (MCPH) is an autosomal recessive condition of reduced head circumference due to a small cerebral cort...
Journal Of Genetics
comment
0
thumb_up
0
On the reversibility of RNA deamination versus RNA methylation: exploring the proximate and ultimate causes
RNA modifications play a crucial role in regulating gene expression, splicing, decoding, translation, and degradation. Amo...
Journal Of Genetics
comment
0
thumb_up
0
Characteristics of the MAPK gene family in and role in response to fungal pathogen infection
The stems of Zizania latifolia, an important vegetable in China, are targeted by the pathogen Ustilago esculenta, triggeri...
Journal Of Genetics
comment
0
thumb_up
0
Mitochondrial genome sequence of Bleeker, 1849 (Syngnathiformes, Syngnathidae) and its phylogenetic placement
The family Syngnathidae includes seahorses, sea dragons, and pipefishes. We sequenced the complete mitochondrial DNA (mtDN...
Journal Of Genetics
comment
0
thumb_up
0
Comparative analysis of the mitochondrial genome of whip scorpion, (Butler, 1872) (Arachnida: Thelyphonidae) with phylogenetic implication
The complete mitogenome of the common Chinese whip scorpion, Typopeltis sinensis (Butler, 1872) was sequenced and compared...
Journal Of Genetics
comment
0
thumb_up
0
A novel partial mRNA-derived duplication of the gene identified in NGS carrier screening
Duplications in the dystrophin gene (DMD) represent a common genetic variation associated with the onset of Duchenne and B...
Journal Of Genetics
comment
0
thumb_up
0
Complete mitochondrial DNA genome of the Indian Chhattisgarh duck and its phylogenetic analysis
The Chhattisgarh duck (Anas platyrhynchos L., 1758) is a native Indian germplasm that provides crucial support for the loc...
Journal Of Genetics
comment
0
thumb_up
0
Transcriptome analysis unveils the intricate dynamics of senescence responses in Himalayan treeline species,
High-altitude ecosystems in the Himalayas exhibit extreme seasonal variations in their vegetation, with summer and winter ...
Journal Of Genetics
comment
0
thumb_up
0
Neuronal expressions of Taxi and Adar are crucial in maintaining the lifespan of
Ageing involves deterioration in physiological processes, such as maintenance of neuronal health, muscle, fat bodies, and ...
Journal Of Genetics
comment
0
thumb_up
0
Characterization and phylogenetic analysis of the mitochondrial genome of (Günther, 1867)
The ornamental fish Amatitlania nigrofasciata, known as the convict or zebra cichlid, is a small Central American tropical...
Journal Of Genetics
comment
0
thumb_up
0
Copy number variation: an important genetic mechanism in-related immunoosseous dysplasia (Schimke type) in Indian patients
Schimke immunoosseous dysplasia (SIOD) is an uncommon inherited genetic disorder resulting from pathogenic variants in the...
Journal Of Genetics
comment
0
thumb_up
0
Full-length transcriptome sequencing and identification of skin colour-associated genes in red tilapia
Red tilapia has gained increasing popularity worldwide in the commercial aquaculture production due to its rapid growth an...
Journal Of Genetics
comment
0
thumb_up
0
Mitotic karyotyping and FISH mapping of the gender-specific locus indicate an advanced XY system in
Hippophae rhamnoides ssp. turkestanica, a subdioecious plant inhabiting the cold desert of the Indian Himalaya, has gained...
Journal Of Genetics
comment
0
thumb_up
0
Structural and functional insights from detailed computational analysis of repetome
Eukaryotic proteomes harbour tandem repeats (TRs) of amino acids that may play critical roles in the biology of organisms....
Journal Of Genetics
comment
0
thumb_up
0
Development of specific molecular markers for medicinal peony () with double flower
In China, medicinal Paeonia lactiflora with double flowers (DFs) does not produce seeds, yet it possesses significantly hi...
Journal Of Genetics
comment
0
thumb_up
0
Mitochondrial control region sequences show high genetic connectivity in the brownstripe snapper, (Quoy and Gaimard, 1824) from the east coast of Peninsular Malaysia
The Brownstripe Snapper, Lutjanus vitta (Quoy and Gaimard, 1824) is a commercially important snapper extensively caught in...
Journal Of Genetics
comment
0
thumb_up
0
JAG1 overexpression partially rescues muscle function in a zebrafish model of duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by progressive muscle degeneration and loss o...
Journal Of Genetics
comment
0
thumb_up
0
YY1 as a mediator to enhance the resistance of KRAS mutant colorectal cancer cells to cetuximab
Cetuximab has been indicated as the mainstay of metastatic colorectal cancer (CRC) therapy, of which application was imped...
Journal Of Genetics
comment
0
thumb_up
0
The driver in does not express in the eight pairs of dorsomedial and some other neurons in larval ventral ganglia: a correction
The sev-Gal4 driver is widely used in Drosophila to express the target gene in specific subsets of cells in ommatidial uni...
Journal Of Genetics
comment
0
thumb_up
0
Maternal effect on the inheritance of pericarp colour and grain dimension in rice ( L.)
This study aimed to understand the maternal influence on the inheritance of pericarp colour and grain dimensions in rice, ...
Journal Of Genetics
comment
0
thumb_up
0
Generation of albino C57BL/6J mice by CRISPR embryo editing of the mouse tyrosinase locus
After the arrival of the CRISPR/Cas9 genome editing technology, genetic engineering of model organisms has become much fas...
Journal Of Genetics
comment
0
thumb_up
0
Gonadal mosaicism and paradoxical phenotype in encephalopathy: a case report of two siblings
The neurite extension and migration factor (NEXMIF) encephalopathy is an X-linked disorder that is chara...
Journal Of Genetics
comment
0
thumb_up
0
Characterization and expression patterns of the -like genes in maize
The nonexpressor of pathogenesis-related 1 (NPR1) is the salicylic acid (SA) receptor, which plays an important regulatory...
Journal Of Genetics
comment
0
thumb_up
0
Deletion of noncoding exons 1–2 causes Smith–Magenis syndrome
Smith–Magenis syndrome (SMS) is a complex genetic disorder characterized by developmental delay and a typical behavi...
Journal Of Genetics
comment
0
thumb_up
0
Mapping and gene cloning of a wheat mutant with dwarf and compacted spikes
Plant height and spikelet density are two important traits for wheat (Triticum aestivum L.) yield. The development of whea...
Journal Of Genetics
comment
0
thumb_up
0
Analysis of whole-exome data of nonobese NAFLD patients from India reveals association with new markers on functionally relevant genes and pathways
Nonalcoholic fatty liver disease (NAFLD) occurs in a significant number of nonobese individuals, especially in Asian popul...
Journal Of Genetics
comment
0
thumb_up
0
promoter mutation: a familial study on congenital amegakaryocytic thrombocytopenia
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited bone marrow failure syndrome, which is characterize...
Journal Of Genetics
comment
0
thumb_up
0
Analysis of tandem repeats in seven telomere-to-telomere primate genomes
Tandem repeats (TRs) are highly polymorphic low complexity regions present in all the genomes. The length variation in TRs...
Journal Of Genetics
comment
0
thumb_up
0
is involved in yield-related traits and cell proliferation of maize
Heterotrimeric G-proteins are multifunctional modulators that participate in a wide range of growth and developmental proc...
Journal Of Genetics
comment
0
thumb_up
0
NGLY1-CDDG: report of two cases from India and brief review of literature
N-glycanase1 (NGLY1) deficiency, an autosomal recessive disorder identified a decade ago, is categorized as a congenital d...
Journal Of 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