X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3193) 3193
Publication (303) 303
Newsletter (153) 153
Book Chapter (34) 34
Book Review (33) 33
Newspaper Article (12) 12
Reference (6) 6
Conference Proceeding (3) 3
Data Set (2) 2
Book / eBook (1) 1
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1757) 1757
phenylalanine (1340) 1340
phenylketonuria (1244) 1244
index medicus (1072) 1072
phenylalanine hydroxylase - genetics (964) 964
genetics & heredity (812) 812
phenylketonurias - genetics (802) 802
female (717) 717
mutation (670) 670
male (647) 647
animals (642) 642
biochemistry & molecular biology (596) 596
phenylalanine - blood (522) 522
analysis (408) 408
phenylalanine hydroxylase (396) 396
physiological aspects (367) 367
medicine, research & experimental (354) 354
hyperphenylalaninemia (348) 348
enzymes (347) 347
adult (338) 338
genotype (338) 338
molecular sequence data (332) 332
research (331) 331
child (330) 330
biopterin - analogs & derivatives (324) 324
phenylalanine hydroxylase - metabolism (320) 320
endocrinology & metabolism (319) 319
phenylalanine - metabolism (318) 318
hydroxylases (315) 315
phenotype (315) 315
tetrahydrobiopterin (315) 315
pediatrics (303) 303
base sequence (294) 294
infant, newborn (286) 286
pku (286) 286
genes (284) 284
amino acids (275) 275
metabolism (274) 274
mice (268) 268
genetic aspects (263) 263
phenylketonurias - diagnosis (257) 257
phenylketonurias - enzymology (256) 256
plant sciences (256) 256
tyrosine (242) 242
biosynthesis (241) 241
adolescent (240) 240
phenylalanine ammonia-lyase (235) 235
child, preschool (233) 233
alleles (229) 229
expression (221) 221
phenylketonurias - blood (220) 220
rats (216) 216
infant (202) 202
amino acid sequence (201) 201
gene expression (201) 201
gene (200) 200
kinetics (200) 200
proteins (199) 199
polymerase chain reaction (194) 194
phenylalanine hydroxylase - deficiency (192) 192
phenylketonurias - metabolism (192) 192
mutations (189) 189
phenylketonurias - drug therapy (188) 188
children (187) 187
haplotypes (171) 171
research article (170) 170
diet (168) 168
diagnosis (166) 166
phenylketonurias - diet therapy (162) 162
life sciences (160) 160
biochemistry, general (157) 157
phenylalanine-hydroxylase (157) 157
hydroxylase (156) 156
genetics (155) 155
pregnancy (151) 151
dna mutational analysis (150) 150
biotechnology & applied microbiology (149) 149
polymorphism, restriction fragment length (149) 149
medicine (147) 147
internal medicine (145) 145
phenylalanine-hydroxylase deficiency (143) 143
metabolites (142) 142
article (140) 140
neurosciences (140) 140
genetic research (139) 139
medicine & public health (138) 138
biopterin - therapeutic use (134) 134
exons (133) 133
phenylalanine 4-monooxygenase (132) 132
multidisciplinary sciences (131) 131
deficiency (130) 130
brain (128) 128
metabolic diseases (128) 128
human genetics (126) 126
phenylalanine hydroxylase - chemistry (126) 126
biochemistry (125) 125
models, molecular (122) 122
ammonia (120) 120
phenylketonurias - therapy (118) 118
liver - enzymology (117) 117
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3283) 3283
Chinese (57) 57
Russian (24) 24
French (21) 21
Japanese (20) 20
Spanish (11) 11
German (4) 4
Polish (3) 3
Czech (2) 2
Dutch (2) 2
Ukrainian (2) 2
Finnish (1) 1
Icelandic (1) 1
Italian (1) 1
Latvian (1) 1
Norwegian (1) 1
Portuguese (1) 1
Slovak (1) 1
Slovenian (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 03/2009, Volume 4, Issue 3, p. e4801
Journal Article
Human Mutation, ISSN 1059-7794, 11/2018, Volume 39, Issue 11, pp. 1569 - 1580
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1/2008, Volume 17, Issue 1, pp. 87 - 97
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2017, Volume 100, Issue 2, pp. 257 - 266
Journal Article