X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (14528) 14528
Publication (1718) 1718
Book Review (60) 60
Book Chapter (54) 54
Conference Proceeding (12) 12
Dissertation (6) 6
Book / eBook (3) 3
Data Set (3) 3
Government Document (3) 3
Magazine Article (2) 2
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (9950) 9950
exons (9182) 9182
index medicus (6565) 6565
animals (5030) 5030
female (4726) 4726
molecular sequence data (4612) 4612
male (4562) 4562
base sequence (4382) 4382
mutation (3994) 3994
genetics & heredity (3857) 3857
exons - genetics (3749) 3749
genetic aspects (3114) 3114
genes (3088) 3088
introns (2785) 2785
amino acid sequence (2725) 2725
biochemistry & molecular biology (2602) 2602
adult (2400) 2400
polymerase chain reaction (2277) 2277
expression (2263) 2263
research (2135) 2135
mice (2112) 2112
middle aged (2102) 2102
analysis (2060) 2060
gene expression (2044) 2044
proteins (1983) 1983
genetics (1869) 1869
cell biology (1759) 1759
alleles (1719) 1719
gene (1675) 1675
alternative splicing (1661) 1661
multidisciplinary sciences (1554) 1554
dna (1502) 1502
research article (1474) 1474
sequence analysis, dna (1441) 1441
genotype (1440) 1440
dna mutational analysis (1407) 1407
identification (1393) 1393
aged (1390) 1390
genomics (1380) 1380
rna, messenger - genetics (1355) 1355
phenotype (1348) 1348
genetic research (1332) 1332
oncology (1263) 1263
cloning, molecular (1244) 1244
mutations (1155) 1155
genomes (1145) 1145
cancer (1137) 1137
rna, messenger - metabolism (1115) 1115
pedigree (1090) 1090
phylogeny (1060) 1060
child (1012) 1012
sequence alignment (1008) 1008
rna (1003) 1003
medicine (997) 997
adolescent (991) 991
protein (991) 991
article (962) 962
physiological aspects (960) 960
introns - genetics (956) 956
polymorphism, genetic (946) 946
neurosciences (917) 917
transcription, genetic (908) 908
gene mutations (901) 901
immunology (898) 898
life sciences (898) 898
polymorphism, single nucleotide (887) 887
evolution (885) 885
messenger-rna (865) 865
sequence homology, amino acid (849) 849
chromosome mapping (820) 820
rna splicing (817) 817
reverse transcriptase polymerase chain reaction (816) 816
deoxyribonucleic acid--dna (811) 811
science (808) 808
transcription (804) 804
pathology (771) 771
polymorphism (769) 769
biology (766) 766
mutation - genetics (761) 761
genetic predisposition to disease (755) 755
gene frequency (752) 752
genetic variation (752) 752
dna - genetics (747) 747
promoter regions, genetic (743) 743
cell line (731) 731
gene deletion (726) 726
biotechnology & applied microbiology (723) 723
splicing (721) 721
messenger rna (717) 717
cloning (711) 711
sequence (703) 703
child, preschool (673) 673
evolution, molecular (658) 658
cells (657) 657
disease (657) 657
molecular biology (646) 646
rats (644) 644
point mutation (626) 626
tumors (623) 623
risk factors (619) 619
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (14515) 14515
Chinese (28) 28
Japanese (9) 9
French (5) 5
Russian (3) 3
Spanish (3) 3
German (2) 2
Korean (2) 2
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 02/2011, Volume 96, Issue 2, pp. 296 - 307
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2016, Volume 24, Issue 1, pp. 44 - 50
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2012, Volume 109, Issue 34, pp. 13763 - 13768
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2010, Volume 285, Issue 41, pp. 31537 - 31547
Journal Article
Molecular Therapy, ISSN 1525-0016, 11/2019, Volume 27, Issue 11, pp. 2005 - 2017
Mutations in the ( ) gene and consequent loss of dystrophin cause Duchenne muscular dystrophy (DMD). A promising therapy for DMD, single-exon skipping using... 
Becker muscular dystrophy | humanized mouse | PMO | exon skipping | antisense oligonucleotide | Duchenne muscular dystrophy | phosphorodiamidate morpholino oligomer | BMD | DMD | exons 45–55 | dystrophin
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 2007, Volume 15, Issue 7, pp. 757 - 763
Journal Article
Hemoglobin, ISSN 0363-0269, 6/2015, Volume 39, Issue 3, pp. 209 - 210
Abstract We report a case of α+-thalassemia (α+-thal) trait in a Chinese-Canadian family caused by a novel frameshift mutation of the α2-globin gene,... 
α-Thalassemia (α-thal) | frameshift | point mutation | Frameshift Mutation | Exons | Humans | Erythrocyte Indices | Genotype | Infant | Male | Phenotype | Codon | DNA Mutational Analysis | alpha-Globins - genetics | alpha-Thalassemia - diagnosis | Adult | Female | alpha-Thalassemia - genetics
Journal Article
Journal of Genetics, ISSN 0022-1333, 12/2017, Volume 96, Issue 6, pp. 933 - 939
Journal Article
by Liu, N and Zhang, Z and Shan, X and Wang, L and Cui, S
Tissue Antigens, ISSN 0001-2815, 02/2013, Volume 81, Issue 2, pp. 121 - 123
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1828, pp. 141 - 150
Antisense oligonucleotide-mediated exon skipping is a promising therapeutic approach for the treatment of various genetic diseases and a therapy which has... 
Direct reprogramming | Duchenne/Becker muscular dystrophy (DMD/BMD) | Golodirsen | Exon skipping | Eteplirsen | NS-065/NCNP-01 | Myotube | Dystrophin | Fibroblast | Phosphorodiamidate morpholino oligomer (PMO) | NS-065 | Duchenne | BMD | Becker muscular dystrophy (DMD | NCNP-01
Journal Article
International Journal of Immunogenetics, ISSN 1744-3121, 04/2013, Volume 40, Issue 2, pp. 154 - 155
Journal Article