×
Close
註冊
登入
主页
医学图书S馆
医学图书D馆
活动
Upcoming Events
Past Events
用户工具
用户指南
语言
English
中文/ Chinese
French
Português
Español
Arabic
Russian
×
Close
mdla_1
mdla_2
mdla_3
mdla_4
mdla_5
mdla_6
分类
Genetics & Heredity
14711
Global Medical University
5020
Allergy
1783
Anatomy & Morphology
1527
Andrology
414
Anesthesia & Intensive Care
1214
Anesthesiology
5442
Audiology & Speech-Language Pathology
332
Behavioral Sciences
100
Biochemical Research Methods
6818
Biochemistry & Molecular Biology
29335
Biodiversity Conservation
288
Biology
8218
Biophysics
8099
Biotechnology & Applied Microbiology
8197
Cardiac & Cardiovascular Systems
30752
Cardiovascular & Respiratory Systems
1391
Cell & Tissue Engineering
654
Cell Biology
10825
Chemistry, Analytical
4216
Chemistry, Applied
11003
Chemistry, Medicinal
8487
Chemistry, Multidisciplinary
18503
Clinical Immunology & Infectious Disease
442
Clinical Medicine
8751
Clinical Neurology
16238
Clinical Psychology & Psychiatry
1298
Critical Care Medicine
3153
Dentistry, Oral Surgery & Medicine
12959
Dermatology
7601
Developmental Biology
6915
Ecology
645
Education, Scientific Disciplines
1886
Emergency Medicine
3981
Endocrinology, Metabolism & Nutrition
23582
Engineering, Biomedical
3586
Entomology
425
Environmental Medicine & Public Health
4623
Evolutionary Biology
254
Gastroenterology & Hepatology
11883
General & Internal Medicine
6948
Geriatrics & Gerontology
5022
Gerontology
338
Health Care Sciences & Services
15636
Health Policy & Services
594
Hematology
5456
Immunology
24666
Infectious Diseases
13671
Integrative & Complementary Medicine
2758
Medical Ethics
1146
Medical Informatics
2117
Medical Laboratory Technology
433
Medicine, General & Internal
44233
Medicine, Legal
493
Medicine, Research & Experimental
17436
Microbiology
22778
Mycology
0
Nanoscience & Nanotechnology
5039
Neuroimaging
1293
Neurology
4396
Neurosciences
38942
Nursing
9355
Nutrition & Dietetics
7802
Obstetrics & Gynecology
8102
Oncology
51594
Ophthalmology
9493
Optics
4025
Orthopedics
11367
Orthopedics, Rehabilitation & Sports Medicine
1729
Otolaryngology
1505
Otorhinolaryngology
4791
Parasitology
1040
Pathology
4888
Pediatrics
21065
Peripheral Vascular Disease
4693
Pharmacology & Pharmacy
33972
Pharmacology/Toxicology
12027
Physiology
8875
Polymer Science
539
Primary Health Care
795
Psychiatry
18891
Psychology
5053
Psychology, Applied
92
Psychology, Biological
335
Psychology, Clinical
785
Psychology, Developmental
222
Psychology, Educational
149
Psychology, Experimental
122
Psychology, Mathematical
0
Psychology, Multidisciplinary
1590
Psychology, Psychoanalysis
41
Psychology, Social
114
Public Health & Health Care Science
2227
Public, Environmental & Occupational Health
26926
Quantum Science & Technology
0
Radiology, Nuclear Medicine & Imaging
12032
Radiology, Nuclear Medicine & Medical Imaging
7772
Rehabilitation
2967
Remote Sensing
0
Reproductive Biology
2745
Reproductive Medicine
1131
Research/Laboratory Medicine & Medical Technology
3872
Respiratory System
7101
Rheumatology
5751
Social Sciences, Biomedical
1176
Substance Abuse
2676
Surgery
33275
Toxicology
4241
Transplantation
927
Tropical Medicine
314
Urology & Nephrology
12745
Veterinary Sciences
35
Virology
2383
Zoology
0
渠道
HUMAN HEREDITY
33
Genetics
5
NEJM Genetics
3
Medrxiv - Genetic And Genomic Medicine
1730
CANCER GENE THERAPY
352
CHROMOSOMA
65
CLINICAL GENETICS
118
CURRENT GENETICS
107
CURRENT OPINION IN GENETICS & DEVELOPMENT
245
EPIGENETICS & CHROMATIN
127
EPIGENOMICS
33
EPILEPSIA
211
FRONTIERS IN GENETICS
5400
GENE THERAPY
176
GENETICS IN MEDICINE
104
GENOME MEDICINE
301
GENOMICS PROTEOMICS & BIOINFORMATICS
211
HUMAN GENETICS
330
HUMAN MUTATION
121
JOURNAL OF HUMAN GENETICS
275
JOURNAL OF MEDICAL GENETICS
384
NATURE REVIEWS GENETICS
310
NPJ GENOMIC MEDICINE
178
ORPHANET JOURNAL OF RARE DISEASES
787
ANNALS OF HUMAN GENETICS
24
CYTOGENETIC AND GENOME RESEARCH
97
G3-GENES GENOMES GENETICS
19
GENETIC EPIDEMIOLOGY
30
HUMAN GENOMICS
224
INTERNATIONAL JOURNAL OF IMMUNOGENETICS
23
JOURNAL OF EVOLUTIONARY BIOLOGY
120
JOURNAL OF GENETIC COUNSELING
152
PSYCHIATRIC GENETICS
131
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
270
FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES
17
GENETICS AND MOLECULAR RESEARCH
10
GLOBAL MEDICAL GENETICS
129
INTERNATIONAL JOURNAL OF NEONATAL SCREENING
89
JOURNAL OF COMMUNITY GENETICS
180
NON-CODING RNA
125
FUNCTIONAL & INTEGRATIVE GENOMICS
486
GENETICA
94
IMMUNOGENETICS
128
JOURNAL OF APPLIED GENETICS
198
JOURNAL OF GENETICS
178
RUSSIAN JOURNAL OF GENETICS
381
SCI时时刷
search
全部
推荐
+
Methods and software to analyze gene-environment interactions under a case-mother - control-mother design with partially missing child genotype
Introduction: The case-mother - control-mother design allows to study fetal and maternal genetic factors together with env...
Human Heredity
comment
0
thumb_up
0
A common variant of ARRB2 promoter region Associated with the Prognosis of Heart Failure
Introduction The role of ARRB2 in cardiovascular disease has recently gained increasing attention. However, the associatio...
Human Heredity
comment
0
thumb_up
0
Polymorphisms of placental iodothyronine deiodinase genes in a rural area of Northern China with high prevalence of neural tube defects
Introduction: We have reported that high total homocysteine (tHCY), and the coexistence of inadequate thyroid hormones in ...
Human Heredity
comment
0
thumb_up
0
Identification of a hypoxia-related signature as candidate detector for schizophrenia based on genome-wide gene expression
Introduction: Schizophrenia (SCZ), a severe neuropsychiatric disorder with high genetic susceptibility, has high rates of ...
Human Heredity
comment
0
thumb_up
0
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review
<b><i>Background:</i></b> Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that resu...
Human Heredity
comment
0
thumb_up
0
A comprehensive study of mutations in PAH, QDPR, PTS, and PCD genes in Iranian patients with Hyperphenylalaninemia; A systematic review
Background: Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that results from a deficiency in the phenylala...
Human Heredity
comment
0
thumb_up
0
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR
<b><i>Objective:</i></b> Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked geneti...
Human Heredity
comment
0
thumb_up
0
The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?
<b><i>Purpose:</i></b> Polycythemia vera is a hematological malignancy characterized by the overpr...
Human Heredity
comment
0
thumb_up
0
Reduction of missed diagnosis of G6PD deficiency in heterozygous females by G6PD/6PGD ratio assay combined with ARMS-PCR
Objective: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder that results in impaired en...
Human Heredity
comment
0
thumb_up
0
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure
<b><i>Introduction:</i></b> The role of neuraminidases in cardiovascular disease has recently gain...
Human Heredity
comment
0
thumb_up
0
The prevalence of JAK2 exon12 mutations in Vietnamese patients with JAK2 V617F-negative polycythemia vera: frequent or rare?
Purpose Polycythemia vera is a hematological malignancy characterized by the overproduction of red blood cells in the bone...
Human Heredity
comment
0
thumb_up
0
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-eclampsia
Objectives: Impairment of mitochondrial function caused by pathogenic mitochondrial DNA (mtDNA) mutations has been found t...
Human Heredity
comment
0
thumb_up
0
Common variants in Neuraminidases genes contribute to predisposition to and progression of chronic heart failure
Introduction The role of neuraminidases in cardiovascular disease has recently gained increasing attention. However, the a...
Human Heredity
comment
0
thumb_up
0
Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes
Introduction: Increasingly, logistic regression methods for genetic association studies of binary phenotypes must be able...
Human Heredity
comment
0
thumb_up
0
Identification of a novel mutation in patients with type A insulin resistance syndrome
Introduction: Type A insulin resistance syndrome is a rare type of congenital insulin resistance often caused by heterozyg...
Human Heredity
comment
0
thumb_up
0
Identification of CHEK2 Germline Mutations in BRCA1/2- and PALB2-Negative Breast and Ovarian Cancer Patients
<b><i>Introduction:</i></b> The <i>CHEK2</i> gene is known to be an important signal t...
Human Heredity
comment
0
thumb_up
0
The Mitochondrial tRNAAsp T7561C, tRNAHis C12153T, and A12172G Mutations May Be Associated with Essential Hypertension in a Han Chinese Pedigree
<b><i>Objectives:</i></b> Mutations in mitochondrial tRNA (mt-tRNA) are the important causes for m...
Human Heredity
comment
0
thumb_up
0
50th European Mathematical Genetics Meeting (EMGM) 2022
...
Human Heredity
comment
0
thumb_up
0
The mitochondrial tRNAAsp T7561C, tRNAHis C12153T and A12172G mutations may be associated with essential hypertension in a Han Chinese pedigree
Objectives: Mutations in mitochondrial tRNA (mt-tRNA) are the important causes for maternally inherited hypertension, howe...
Human Heredity
comment
0
thumb_up
0
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts
Enamel hypoplasia causes reduction in the thickness of affected enamel and is one of the most common dental anomalies. Thi...
Human Heredity
comment
0
thumb_up
0
Identification of CHEK2 germline mutations in BRCA1/2 and PALB2 negative breast and ovarian cancer patients
Introduction: The CHEK2 gene is known to be an important signal transducer involved in DNA repair, apoptosis, or cell cycl...
Human Heredity
comment
0
thumb_up
0
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy
Objectives: Dilated cardiomyopathy (DCM) is a complex cardiovascular disease with unknown etiology. Although nuclear genes...
Human Heredity
comment
0
thumb_up
0
49th European Mathematical Genetics Meeting (EMGM) 2021
...
Human Heredity
comment
0
thumb_up
0
Association of PNPLA3 I148M with Liver Disease Biomarkers in Latinos
<b><i>Introduction:</i></b> Liver disease accounts for approximately 2 million deaths per year wor...
Human Heredity
comment
0
thumb_up
0
Family history of breast cancer is associated with elevated risk of prostate cancer: evidence for shared genetic risks
Introduction: Although breast and prostate cancers arise in different organs and are more frequent in the opposite sex, mu...
Human Heredity
comment
0
thumb_up
0
Association of PNPLA3 I148M with liver disease biomarkers in Latinos
Introduction. Liver disease accounts for approximately 2 million deaths per year worldwide. The majority of liver diseases...
Human Heredity
comment
0
thumb_up
0
Exome-Wide Pan-Cancer Analysis of Germline Variants in 8,719 Individuals Finds Little Evidence of Rare Variant Associations
<b><i>Background:</i></b> Many cancer types show considerable heritability, and extensive research...
Human Heredity
comment
0
thumb_up
0
Importance of Family History in the Era of Exome Analysis: A Report of a Family with Multiple Concurrent Genetic Diseases
Multiple familial diseases in a single patient often present with overlapping symptomatology that confers difficulty in de...
Human Heredity
comment
0
thumb_up
0
Meta-Analysis of Joint Test of SNP and SNP-Environment Interaction with Heterogeneity
Many complex diseases are caused by single nucleotide polymorphisms (SNPs), environmental factors, and the interaction bet...
Human Heredity
comment
0
thumb_up
0
PhosSNPs-Regulated Gene Network and Pathway Significant for Rheumatoid Arthritis
<b><i>Objectives:</i></b> Peripheral blood mononuclear cells (PBMCs) are critical for immunity and...
Human Heredity
comment
0
thumb_up
0
阅读更多
Modal title
×
Modal title
×
分享
登入
Global News and Health Forum
Join Now!
馬上登入
記住我
忘記密碼?
或者使用
Linkedin