Keyphrases
Usher Syndrome
92%
Molecular Genetics
54%
Hearing Impairment
45%
Auditory System
30%
Physical Mapping
30%
USH2
27%
Alport Syndrome
23%
Connexin 26
20%
Usher Genes
19%
Mouse Model
19%
Positional Cloning
19%
Conditional Knockout Mouse Model
18%
Retinitis pigmentosa
17%
Childhood Deafness
17%
Genetic Studies
17%
Basement Membrane
17%
Usherin
16%
Syndrome Type
15%
USH2A
14%
Nonsyndromic
14%
Vestibular Disorders
14%
X-linked
13%
Photoreceptor Cells
13%
Function Expression
13%
Cochlea
13%
USH1B
13%
Clinical Type
13%
Collagen
13%
Genetic Counseling
11%
Glomerulonephritis
11%
Yeast Artificial Chromosome
10%
Effective Method
10%
Recent Advances
10%
Diagnostic Accuracy
10%
Professional Relationships
10%
GJB2
10%
Non-syndromic Hearing Loss
10%
35delG
10%
Extracellular Matrix Protein 1 (ECM1)
9%
Deafness
9%
Cochlear Cells
8%
Retinal Cells
8%
DNA Fragments
7%
Alport
6%
Collagen Chains
6%
Delayed Onset
6%
Immunohistology
6%
Sudden Sensorineural Hearing Loss (SSNHL)
6%
Histology
6%
Heterozygote
6%
Secreted Molecules
6%
American Population
6%
MYO7A
6%
Hereditary Disease
6%
Genetic Loci
6%
Molecular Biology
5%
Professional Will
5%
Integrated Teams
5%
Genetic Basis
5%
Regulatory Region
5%
Branchio-oto-renal Syndrome
5%
Disease-causing mutations
5%
Long-term Commitment
5%
Nephritis
5%
Spatial Organization
5%
Unconventional Myosin
5%
Temporal Organization
5%
Vision Function
5%
Inner Retina
5%
Lens of the Eye
5%
Gene Products
5%
Visual Manifestations
5%
Gene-based
5%
Cloning Strategy
5%
Maximum Efficiency
5%
Chromosome 1q
5%
Normal Hearing
5%
Genetic Diagnosis
5%
Inner Ear
5%
Hearing Function
5%
What-if
5%
Sequence Tagged Sites
5%
Vestibular Function
5%
Congenital Hearing Loss
5%
Disease Diagnosis
5%
Coding Region
5%
Family Resources
5%
Biochemistry, Genetics and Molecular Biology
Genetics
100%
Molecular Genetics
76%
Candidate Gene
45%
Retinitis pigmentosa
43%
Gene Linkage
41%
USH2A
41%
Clinical Study
34%
Genetic Counseling
32%
Mouse Model
29%
Yeast Artificial Chromosome
27%
Gene Loss
25%
Genetic Disorder
22%
Mouse
20%
Gene Mapping
20%
Gene Knockout
20%
GJB2
20%
Knockout Mouse
20%
Gene Location
20%
Basement Membrane
18%
MYO7A
17%
Gene Locus
17%
Jumping
16%
Animal Model
15%
Genetic Carrier
13%
Heterozygote
13%
Molecular Biology
13%
Chromosome 1
12%
Extracellular Matrix Protein
10%
Gene Product
10%
Contig
10%
Vestibular Function
10%
Sequence-Tagged Site
10%
Regulatory Region
10%
Conserved Sequence
9%
DNA Sequence
9%
Gene Targeting
8%
Chromosome 1q
8%
Gene Polymorphism
6%
Type IV Collagen
6%
Brain Stem Response
6%
Laboratory Test
6%
Fibronectin
6%
Laminin
6%
Gene Linkage Disequilibrium
6%
Heteroduplex Analysis
6%
Linkage Analysis
6%
Membrane Protein
6%
Protein Sequencing
6%
Hearing
6%
Marker Gene
6%
Stem Cell
6%
Proteoglycan
6%
CpG Island
6%
Connexin
6%
Entactin
6%
Neuroscience
Auditory System
69%
Sensation of Hearing
62%
Retinitis pigmentosa
52%
Extracellular Matrix
34%
Genetic Mapping
34%
Gene Location
32%
Gene Locus
27%
Regulatory Region
20%
Gene Product
20%
Photoreceptor Cell
20%
Basement Membrane
20%
Promoter Region
20%
Sequence-Tagged Site
20%
Vestibular Function
20%
Contig
20%
Matrix Protein
20%
Sensorineural Hearing Loss
20%
Gene Knockout
20%
Cochlea
20%
Collagen Type 4
15%
Hearing Loss
13%
Epileptic Absence
13%
Gene Delivery
10%
Chromosome 1q
9%
Stem Cell
6%
Proteoheparan Sulfate
6%
Entactin
6%
Fibronectin
6%
Auditory Brainstem Response
6%
Laminin
6%
DNA Polymorphism
6%
Temporal Bone
6%
Green Fluorescent Protein
6%
Perineurium
6%
Integrin
6%
Ganglion Cell
6%
Autosomal Recessive Disorder
6%
Nuclear Factor
6%
Gene Expression System
6%
Synthetic Peptide
6%
Spiral Ganglion
6%
Mutagenesis
6%
Antiserum
6%