Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
237 | 43811 | 43.1 | 77% |
Classes in level above (level 4) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
0 | 3633673 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//MED |
Classes in level below (level 2) |
ID, lev. below |
Publications | Label for level below |
---|---|---|
201 | 20439 | MELAS//MITOCHONDRIAL DNA//LEBERS HEREDITARY OPTIC NEUROPATHY |
1290 | 8210 | PERMEABILITY TRANSITION//BARTH SYNDROME//UNCOUPLING PROTEIN |
1315 | 8032 | PROTEIN TRANSLOCATION//PROTEIN IMPORT//SECA |
1833 | 5655 | GLUCOSE TRANSPORTER//WARBURG EFFECT//GLUT1 |
3239 | 1475 | VDAC//MITOCHONDRIAL PORIN//VOLTAGE DEPENDENT ANION SELECTIVE CHANNEL |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | MITOCHONDRIA | Author keyword | 887 | 18% | 10% | 4364 |
2 | MELAS | Author keyword | 459 | 81% | 1% | 278 |
3 | MITOCHONDRIAL DISEASE | Author keyword | 399 | 66% | 1% | 373 |
4 | MITOCHONDRIAL DNA | Journal | 397 | 59% | 1% | 444 |
5 | LEBERS HEREDITARY OPTIC NEUROPATHY | Author keyword | 389 | 90% | 0% | 172 |
6 | MITOCHONDRIAL GENOME | Author keyword | 373 | 51% | 1% | 530 |
7 | COMPLEX I | Author keyword | 318 | 54% | 1% | 414 |
8 | LEIGH SYNDROME | Author keyword | 317 | 83% | 0% | 181 |
9 | LHON | Author keyword | 292 | 93% | 0% | 109 |
10 | PROTEIN IMPORT | Author keyword | 267 | 60% | 1% | 290 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | MITOCHONDRIA | 887 | 18% | 10% | 4364 | Search MITOCHONDRIA | Search MITOCHONDRIA |
2 | MELAS | 459 | 81% | 1% | 278 | Search MELAS | Search MELAS |
3 | MITOCHONDRIAL DISEASE | 399 | 66% | 1% | 373 | Search MITOCHONDRIAL+DISEASE | Search MITOCHONDRIAL+DISEASE |
4 | MITOCHONDRIAL DNA | 389 | 22% | 4% | 1569 | Search MITOCHONDRIAL+DNA | Search MITOCHONDRIAL+DNA |
5 | LEBERS HEREDITARY OPTIC NEUROPATHY | 389 | 90% | 0% | 172 | Search LEBERS+HEREDITARY+OPTIC+NEUROPATHY | Search LEBERS+HEREDITARY+OPTIC+NEUROPATHY |
6 | MITOCHONDRIAL GENOME | 373 | 51% | 1% | 530 | Search MITOCHONDRIAL+GENOME | Search MITOCHONDRIAL+GENOME |
7 | COMPLEX I | 318 | 54% | 1% | 414 | Search COMPLEX+I | Search COMPLEX+I |
8 | LEIGH SYNDROME | 317 | 83% | 0% | 181 | Search LEIGH+SYNDROME | Search LEIGH+SYNDROME |
9 | LHON | 292 | 93% | 0% | 109 | Search LHON | Search LHON |
10 | PROTEIN IMPORT | 267 | 60% | 1% | 290 | Search PROTEIN+IMPORT | Search PROTEIN+IMPORT |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | KEARNS SAYRE SYNDROME | 1219 | 83% | 2% | 699 |
2 | YEAST MITOCHONDRIA | 994 | 69% | 2% | 860 |
3 | INNER MEMBRANE | 947 | 56% | 3% | 1153 |
4 | PRECURSOR PROTEINS | 922 | 74% | 2% | 677 |
5 | PREPROTEIN TRANSLOCASE | 905 | 92% | 1% | 364 |
6 | HEREDITARY OPTIC NEUROPATHY | 873 | 68% | 2% | 771 |
7 | STROKE LIKE EPISODES | 867 | 83% | 1% | 492 |
8 | ADP ATP CARRIER | 756 | 78% | 1% | 502 |
9 | DNA MUTATIONS | 611 | 74% | 1% | 453 |
10 | LEIGH SYNDROME | 583 | 76% | 1% | 405 |
Journals |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MITOCHONDRIAL DNA | 397 | 59% | 1% | 444 |
2 | MITOCHONDRION | 230 | 43% | 1% | 411 |
3 | JOURNAL OF BIOENERGETICS AND BIOMEMBRANES | 168 | 28% | 1% | 513 |
4 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 113 | 17% | 1% | 596 |
5 | CURRENT GENETICS | 51 | 12% | 1% | 412 |
6 | SOMATIC CELL GENETICS | 3 | 11% | 0% | 26 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
How mitochondria produce reactive oxygen species | 2009 | 1259 | 108 | 44% |
The mitochondrial permeability transition pore: Molecular nature and role as a target in cardioprotection | 2015 | 12 | 132 | 60% |
Disturbed mitochondrial dynamics and neurodegenerative disorders | 2015 | 11 | 201 | 65% |
The mitochondrial permeability transition: A current perspective on its identity and role in ischaemia/reperfusion injury | 2015 | 10 | 187 | 66% |
Mitochondrial diseases in man and mouse | 1999 | 1822 | 84 | 73% |
Translocation of proteins into mitochondria | 2007 | 611 | 185 | 90% |
THE MITOCHONDRIAL PERMEABILITY TRANSITION | 1995 | 1780 | 442 | 68% |
Mitochondrial fusion and fission in cell life and death | 2010 | 355 | 129 | 84% |
Mitochondrial form and function | 2014 | 56 | 124 | 65% |
Mitochondria: Dynamic organelles in disease, aging, and development | 2006 | 653 | 82 | 90% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | NIJMEGEN MITOCHONDRIAL DISORDERS | 253 | 74% | 0.4% | 189 |
2 | MITOCHONDRIAL GRP | 197 | 59% | 0.5% | 218 |
3 | MITOENGN | 82 | 71% | 0.2% | 66 |
4 | ZBMZ | 79 | 60% | 0.2% | 86 |
5 | BIOMEMBRANES BIOENERGET | 70 | 48% | 0.2% | 108 |
6 | DUNN HUMAN NUTR UNIT | 65 | 32% | 0.4% | 167 |
7 | MITOCHONDRIAL BIOL UNIT | 63 | 49% | 0.2% | 93 |
8 | WELLCOME TRUST MITOCHONDRIAL | 61 | 58% | 0.2% | 70 |
9 | ZENTRUM BIOL CHEM | 59 | 65% | 0.1% | 57 |
10 | MEMBRANE TRANSPORT BIOPHYS | 45 | 69% | 0.1% | 38 |
Related classes at same level (level 3) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000004360 | F 1 ATPASE//ATP SYNTHASE//V ATPASE |
2 | 0.0000002099 | NM23//RIBONUCLEOTIDE REDUCTASE//DEOXYCYTIDINE KINASE |
3 | 0.0000002079 | RNA-A PUBLICATION OF THE RNA SOCIETY//RIBOZYME//NUCLEIC ACIDS RESEARCH |
4 | 0.0000002076 | RESVERATROL//C ELEGANS//CAENORHABDITIS ELEGANS |
5 | 0.0000001965 | HEPATIC ENCEPHALOPATHY//KETOGENIC DIET//CARNITINE |
6 | 0.0000001946 | AUTOPHAGY//TRAIL//APOPTOSIS |
7 | 0.0000001912 | HUNTINGTONS DISEASE//POLYGLUTAMINE//HUNTINGTIN |
8 | 0.0000001831 | PEROXISOME//ADRENOLEUKODYSTROPHY//PEROXISOMES |
9 | 0.0000001818 | CREATINE//MAGNETIC RESONANCE SPECTROSCOPY//LITHIUM |
10 | 0.0000001784 | MEDICINE, LEGAL//FORENSIC SCIENCE INTERNATIONAL-GENETICS//FORENSIC SCIENCE |