X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (183) 183
humans (149) 149
ophthalmology (148) 148
male (97) 97
genetics & heredity (94) 94
female (90) 90
mutation (72) 72
animals (68) 68
pedigree (59) 59
mice (49) 49
adult (47) 47
biochemistry & molecular biology (42) 42
middle aged (39) 39
eye diseases (37) 37
dna mutational analysis (34) 34
sense organs (33) 33
molecular sequence data (31) 31
base sequence (30) 30
genetics (30) 30
genetic aspects (29) 29
phenotype (27) 27
child (26) 26
research (24) 24
adolescent (23) 23
expression (23) 23
gene (23) 23
aged (22) 22
corneal dystrophies, hereditary - genetics (22) 22
eye proteins - genetics (22) 22
proteins (22) 22
analysis (21) 21
child, preschool (21) 21
genes (21) 21
mutations (21) 21
research article (21) 21
apoptosis (20) 20
cell biology (20) 20
genetic linkage (20) 20
polymerase chain reaction (20) 20
chromosome mapping (19) 19
medicine, research & experimental (19) 19
retina (19) 19
gene expression (18) 18
genetic structures (18) 18
protein (18) 18
cell line (17) 17
retinal degeneration (17) 17
electroretinography (16) 16
point mutation (16) 16
extracellular matrix proteins - genetics (14) 14
family (14) 14
retinitis-pigmentosa (14) 14
biotechnology & applied microbiology (13) 13
blotting, western (13) 13
carrier proteins - genetics (13) 13
genotype (13) 13
homozygote (13) 13
infant (13) 13
reverse transcriptase polymerase chain reaction (13) 13
transcription factors - genetics (13) 13
dna (12) 12
dystrophy (12) 12
exons (12) 12
eye (12) 12
gene expression regulation (12) 12
genetic research (12) 12
identification (12) 12
retinitis pigmentosa (12) 12
retinitis pigmentosa - genetics (12) 12
transforming growth factor beta - genetics (12) 12
amino acid sequence (11) 11
biology (11) 11
blindness (11) 11
degeneration (11) 11
disease (11) 11
gene mutations (11) 11
macular degeneration (11) 11
mice, inbred c57bl (11) 11
multidisciplinary sciences (11) 11
photoreceptors (11) 11
retinal degeneration - genetics (11) 11
syndrome (11) 11
apoptosis - physiology (10) 10
beta-ig-h3 (10) 10
cataract - genetics (10) 10
cells (10) 10
human genetics (10) 10
leber congenital amaurosis (10) 10
macular degeneration - genetics (10) 10
tomography, optical coherence (10) 10
alleles (9) 9
cells, cultured (9) 9
cone-rod dystrophy (9) 9
corneal dystrophies, hereditary - pathology (9) 9
disease models, animal (9) 9
extracellular matrix proteins - metabolism (9) 9
fluorescein angiography (9) 9
genes, dominant (9) 9
genetic disorders (9) 9
growth-factor-beta (9) 9
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Klionsky, Daniel J and Abdelmohsen, Kotb and Abe, Akihisa and Abedin, Md Joynal and Abeliovich, Hagai and Acevedo Arozena, Abraham and Adachi, Hiroaki and Adams, Christopher M and Adams, Peter D and Adeli, Khosrow and Adhihetty, Peter J and Adler, Sharon G and Agam, Galila and Agarwal, Rajesh and Aghi, Manish K and Agnello, Maria and Agostinis, Patrizia and Aguilar, Patricia V and Aguirre-Ghiso, Julio and Airoldi, Edoardo M and Ait-Si-Ali, Slimane and Akematsu, Takahiko and Akporiaye, Emmanuel T and Al-Rubeai, Mohamed and Albaiceta, Guillermo M and Albanese, Chris and Albani, Diego and Albert, Matthew L and Aldudo, Jesus and Algül, Hana and Alirezaei, Mehrdad and Alloza, Iraide and Almasan, Alexandru and Almonte-Beceril, Maylin and Alnemri, Emad S and Alonso, Covadonga and Altan-Bonnet, Nihal and Altieri, Dario C and Alvarez, Silvia and Alvarez-Erviti, Lydia and Alves, Sandro and Amadoro, Giuseppina and Amano, Atsuo and Amantini, Consuelo and Ambrosio, Santiago and Amelio, Ivano and Amer, Amal O and Amessou, Mohamed and Amon, Angelika and An, Zhenyi and Anania, Frank A and Andersen, Stig U and Andley, Usha P and Andreadi, Catherine K and Andrieu-Abadie, Nathalie and Anel, Alberto and Ann, David K and Anoopkumar-Dukie, Shailendra and Antonioli, Manuela and Aoki, Hiroshi and Apostolova, Nadezda and Aquila, Saveria and Aquilano, Katia and Araki, Koichi and Arama, Eli and Aranda, Agustin and Araya, Jun and Arcaro, Alexandre and Arias, Esperanza and Arimoto, Hirokazu and Ariosa, Aileen R and Armstrong, Jane L and Arnould, Thierry and Arsov, Ivica and Asanuma, Katsuhiko and Askanas, Valerie and Asselin, Eric and Atarashi, Ryuichiro and Atherton, Sally S and Atkin, Julie D and Attardi, Laura D and Auberger, Patrick and Auburger, Georg and Aurelian, Laure and Autelli, Riccardo and Avagliano, Laura and Avantaggiati, Maria Laura and Avrahami, Limor and Awale, Suresh and Azad, Neelam and Bachetti, Tiziana and Backer, Jonathan M and Bae, Dong-Hun and Bae, Jae-sung and Bae, Ok-Nam and Bae, Soo Han and Baehrecke, Eric H and Baek, Seung-Hoon and Baghdiguian, Stephen and Bagniewska-Zadworna, Agnieszka and ... and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Institutionen för medicin och hälsa and Avdelningen för läkemedelsforskning and Avdelningen för cellbiologi
Autophagy, ISSN 1554-8627, 01/2016, Volume 12, Issue 1, pp. 1 - 222
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 08/2013, Volume 91, Issue s252
Purpose To report a new form of juvenile‐onset Best disease associated with optic disc deposits and autosomal dominant inheritance in a three‐generation... 
OPHTHALMOLOGY | Genetic research | Fluorescence | Genetic aspects | Ophthalmology | Genes | Ultrasonic imaging | Medical imaging | Mutation | Web sites | Best disease
Journal Article
Journal Article
Nature Medicine, ISSN 1078-8956, 09/2003, Volume 9, Issue 9, pp. 1180 - 1186
Journal Article