X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (92) 92
humans (79) 79
male (64) 64
female (55) 55
pakistan (36) 36
pedigree (36) 36
adult (34) 34
genetics & heredity (33) 33
mutation (33) 33
biochemistry & molecular biology (32) 32
ophthalmology (32) 32
research article (29) 29
middle aged (28) 28
genetic aspects (26) 26
genetics (25) 25
alleles (23) 23
genes (23) 23
molecular sequence data (20) 20
base sequence (19) 19
case-control studies (17) 17
eye diseases (17) 17
genetic predisposition to disease (17) 17
polymorphism, single nucleotide (17) 17
genotype (16) 16
haplotypes (16) 16
amino acid sequence (15) 15
dna mutational analysis (15) 15
consanguinity (14) 14
gene frequency (14) 14
retinitis pigmentosa (14) 14
mutations (13) 13
analysis (12) 12
genetic association studies (12) 12
homozygote (12) 12
life sciences (12) 12
polymerase chain reaction (12) 12
research (12) 12
retinitis pigmentosa - genetics (12) 12
article (11) 11
association (11) 11
child (11) 11
mutation, missense (11) 11
proteins (11) 11
risk (11) 11
risk factors (11) 11
single-nucleotide polymorphism (11) 11
adolescent (10) 10
asian continental ancestry group - genetics (10) 10
disease (10) 10
gene (10) 10
glaucoma (10) 10
information technology (10) 10
medicine (10) 10
population (10) 10
young adult (10) 10
family (9) 9
genes, recessive (9) 9
genetic structures (9) 9
glaucoma, open-angle - genetics (9) 9
locus (9) 9
multidisciplinary sciences (9) 9
polymorphism (9) 9
polymorphism, single nucleotide - genetics (9) 9
animals (8) 8
dna (8) 8
fundus oculi (8) 8
gene polymorphism (8) 8
genetic linkage (8) 8
genomes (8) 8
genomics (8) 8
glaucoma, angle-closure - genetics (8) 8
open-angle glaucoma (8) 8
polymorphism, genetic (8) 8
retina (8) 8
science (8) 8
blindness (7) 7
child, preschool (7) 7
exons (7) 7
expression (7) 7
heterozygote (7) 7
identification (7) 7
mutation - genetics (7) 7
protein (7) 7
single nucleotide polymorphisms (7) 7
vision (7) 7
aged (6) 6
biology and life sciences (6) 6
deoxyribonucleic acid--dna (6) 6
exfoliation syndrome - genetics (6) 6
gene deletion (6) 6
gene expression (6) 6
genetic research (6) 6
genotypes (6) 6
genotyping (6) 6
glaucoma - genetics (6) 6
hospitals (6) 6
human genetics (6) 6
hypercholesterolemia (6) 6
leber congenital amaurosis (6) 6
phenotype (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Physical Chemistry Chemical Physics : PCCP, ISSN 1463-9076, 01/2018, Volume 20, Issue 46, pp. 29446 - 29451
The use of CdSe/ZnS quantum dots in making biosensors or biomarkers requires them to be water soluble, which can be achieved by conjugating with MAA. We report... 
Zinc sulfides | Water chemistry | Negative ions | Quantum dots | Photoluminescence | Biomarkers | Molecular orbitals | Buffers | Biosensors | Recovery | Positive ions | Electrochemical impedance spectroscopy
Journal Article
Human Genetics, ISSN 0340-6717, 3/2014, Volume 133, Issue 3, pp. 331 - 345
Journal Article
DNA and Cell Biology, ISSN 1044-5498, 07/2018, Volume 37, Issue 7, pp. 609 - 616
The purpose of this study is to investigate the association of variant alleles (rs2781666 and rs2781667) at ARG1 to be involved in the generation of essential... 
essential hypertension | association | polymorphism | gene | arginase | TARGET | ARGINASE I | MYOCARDIAL-INFARCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HAPLOTYPES | CELL BIOLOGY | DISEASE | GENETICS & HEREDITY | NITRIC-OXIDE PRODUCTS | Hypertension | Phenotypes | Typing | Health risks | Arginase | Colorimetry | Gene polymorphism | Risk factors | ARG1 gene | Nitric oxide | Alleles | Catabolites | Polymorphism
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, pp. e0130754 - e0130754
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2015, Volume 10, Issue 12, pp. e0144557 - e0144557
In the present study we determined the association of angiotensin converting enzyme (ACE) and plasminogen activator inhibitor-1 (PAI-1) gene polymorphisms with... 
GENETIC ASSOCIATION | INSERTION/DELETION POLYMORPHISM | MULTIDISCIPLINARY SCIENCES | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | 4G/5G POLYMORPHISM | PROMOTER 4G/5G | DELETION POLYMORPHISM | ANGIOTENSIN-CONVERTING ENZYME | NEPHROPATHY | I/D POLYMORPHISM | ENDOTHELIAL GROWTH-FACTOR | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Male | Diabetic Retinopathy - pathology | Case-Control Studies | INDEL Mutation | Peptidyl-Dipeptidase A - genetics | Pakistan | Adult | Female | Diabetic Retinopathy - etiology | Plasminogen Activator Inhibitor 1 - genetics | Diabetes Mellitus, Type 2 - complications | Severity of Illness Index | Promoter Regions, Genetic | Gene Expression | Genetic Association Studies | Introns | Gene Frequency | Disease Progression | Diabetic Retinopathy - genetics | Polymorphism, Genetic | Alleles | Diabetes Mellitus, Type 2 - pathology | Diabetic retinopathy | Enzyme inhibitors | Angiotensin converting enzyme | Development and progression | Genetic aspects | Health aspects | Genetic polymorphisms | Retinopathy | Genes | Insertion | Retina | Gene deletion | Gene polymorphism | Confidence intervals | Clonal deletion | Peptidyl-dipeptidase A | Deletion | Armed forces | Vascular endothelial growth factor | Genotypes | Enzymes | Phenotypes | Statistical analysis | Diabetes mellitus | Regression analysis | Information technology | Polymerase chain reaction | Hospitals | Plasminogen activator inhibitors | Angiotensin | Diabetes | Polymorphism | Index Medicus
Journal Article
Annals of Human Genetics, ISSN 0003-4800, 07/2019, Volume 83, Issue 4, pp. 285 - 290
Age‐related macular degeneration (AMD) is a disease of the elderly in which central vision is lost because of degenerative changes of the macula. The current... 
AMD | HTRA1 | ARMS2 | CFH | Pakistani population | genetic association study | Macular degeneration | Physiological aspects | Medicine, Experimental | Medical research | Single nucleotide polymorphisms | Analysis | Gene frequency | Alleles | Degeneration | Single-nucleotide polymorphism | Age | Geriatrics | Smoking
Journal Article
Clinical Case Reports, ISSN 2050-0904, 07/2019, Volume 7, Issue 7, pp. 1442 - 1444
Post‐transplant lymphoproliferative disorders are rare but potentially life‐threatening complication of HSCT. Although not frequently reported but PTLD can... 
Epstein‐Barr Virus | aplastic anemia | Hodgkin lymphoma | Cytomegalovirus | Transplants & implants | Anemia | Neutrophils | Family medical history | Patients | Risk factors | Chemotherapy | Technical communication | Stem cells | Hemoglobin | Bone marrow | Lymphomas | Deoxyribonucleic acid--DNA | Neutropenia
Journal Article
by Khor, Chiea Chuen and Do, Tan and Jia, Hongyan and Nakano, Masakazu and George, Ronnie and Abu-Amero, Khaled and Duvesh, Roopam and Chen, Li Jia and Li, Zheng and Nongpiur, Monisha E and Perera, Shamira A and Qiao, Chunyan and Wong, Hon-Tym and Sakai, Hiroshi and De Melo, Mônica Barbosa and Lee, Mei-Chin and SChan, Anita and Azhany, Yaakub and Dao, Thi Lam Huong and Ikeda, Yoko and Perez-Grossmann, Rodolfo A and Zarnowski, Tomasz and Day, Alexander C and Jonas, Jost B and Tam, Pancy O.S and Tran, Tuan Anh and Ayub, Humaira and Akhtar, Farah and Micheal, Shazia and Chew, Paul T.K and Aljasim, Leyla A and Dada, Tanuj and Luu, Tam Thi and Awadalla, Mona S and Kitnarong, Naris and Wanichwecharungruang, Boonsong and Aung, Yee Yee and Mohamed-Noor, Jelinar and Vijayan, Saravanan and Sarangapani, Sripriya and Husain, Rahat and Jap, Aliza and Baskaran, Mani and Goh, David and Su, Daniel H and Wang, Huaizhou and Yong, Vernon K and Yip, Leonard W and Trinh, Tuyet Bach and Makornwattana, Manchima and Nguyen, Thanh Thu and Leuenberger, Edgar U and Park, Ki-Ho and Wiyogo, Widya Artini and SKumar, Rajesh and Tello, Celso and Kurimoto, Yasuo and Thapa, Suman S and Pathanapitoon, Kessara and Salmon, John F and Sohn, Yong Ho and Fea, Antonio and Ozaki, Mineo and Lai, Jimmy S.M and Tantisevi, Visanee and Khaing, Chaw Chaw and Mizoguchi, Takanori and Nakano, Satoko and Kim, Chan-Yun and Tang, Guangxian and Fan, Sujie and Wu, Renyi and Meng, Hailin and Nguyen, Thi Thuy Giang and Tran, Tien Dat and Ueno, Morio and Martinez, Jose Maria and Ramli, Norlina and Aung, Yin Mon and Reyes, Rigo Daniel and Vernon, Stephen A and Fang, Seng Kheong and Xie, Zhicheng and Chen, Xiao Yin and Foo, Jia Nee and Sim, Kar Seng and Wong, Tina T and Quek, Desmond T and Venkatesh, Rengaraj and Kavitha, Srinivasan and Krishnadas, Subbiah R and Soumittra, Nagaswamy and Shantha, Balekudaru and Lim, Boon-Ang and Ogle, Jeanne and Vasconcellos, José P. Cde and Costa, Vital P and Abe, Ricardo Y and De Souza, Bruno B and Sng, Chelvin C and ...
Nature Genetics, ISSN 1061-4036, 05/2016, Volume 48, Issue 5, pp. 556 - 562
Journal Article