MeSH term
Frequency | Condition_Probility | Animals | 11 | 0.0 |
Base Sequence | 8 | 0.0 |
Female | 2 | 0.0 |
Gene Expression | 3 | 0.0 |
Humans | 15 | 0.0 |
Male | 14 | 0.0 |
Mice | 8 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Mice, Transgenic | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 13 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
Comparative Study | 5 | 0.0 |
Haploidy | 3 | 2.0 |
Molecular Sequence Data | 9 | 0.0 |
Organ Specificity | 2 | 0.0 |
Rats | 4 | 0.0 |
Sequence Alignment | 3 | 0.0 |
Sequence Homology, Nucleic Acid | 2 | 0.0 |
Spermatogenesis/*physiology | 2 | 5.0 |
Amino Acid Sequence | 5 | 0.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Mice, Inbred Strains | 2 | 0.0 |
*Chromosome Mapping | 3 | 0.0 |
*Multigene Family | 4 | 0.0 |
Nuclear Proteins/*genetics | 4 | 0.0 |
Protamines/*genetics | 5 | 22.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 2 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Spermatozoa/*metabolism | 2 | 3.0 |
Transcription, Genetic | 2 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Blotting, Northern | 2 | 0.0 |
Cattle | 3 | 0.0 |
Restriction Mapping | 2 | 0.0 |
Species Specificity | 2 | 0.0 |
Testis/metabolism | 3 | 1.0 |
Chromosomes, Human, Pair 16 | 2 | 1.0 |
Chromosomal Proteins, Non-Histone/*genetics | 3 | 9.0 |
Repetitive Sequences, Nucleic Acid | 2 | 0.0 |
Cosmids | 2 | 0.0 |
