Karsten Hokamp
Biographic Data
| ID | 7967967 |
|---|---|
| NAME | Karsten Hokamp |
| GIVEN NAMES | Karsten |
| FAMILY NAME | Hokamp |
| SIGNATURE | HOKAMP K |
| AFFILIATIONS | Trinity College Dublin |
| ORCID | 0000-0001-7464-2370 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 2 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2001 |
| LATEST PUBLICATION YEAR | 2019 |
| H-INDEX | 0 |
Transcriptomic Analysis of Mecp2 Mutant Mice Reveals Differentially Expressed Genes and Altered Mechanisms in Both Blood and Brain
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired communication and movement, cardio-respiratory abnormalities, and seizures. The clinical presentation is typically associated to mutations in the gene coding for the methyl-CpG-binding protein 2 ( MECP2 ), which is a transcription factor. The gene is ubiquitously present in all the cells of the organism with a peak of expression in neurons. For this re…
Initial sequencing and analysis of the human genome
The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and make freely available a draft sequence of the human genome. We also present an initial analysis of the data, describing some of the insights that can be gleaned from the sequence.
No prominent works on this page.
Initial sequencing and analysis of the human genome
The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and make freely available a draft sequence of the human genome. We also present an initial analysis of the data, describing some of the insights that can be gleaned from the sequence.
Transcriptomic Analysis of Mecp2 Mutant Mice Reveals Differentially Expressed Genes and Altered Mechanisms in Both Blood and Brain
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired communication and movement, cardio-respiratory abnormalities, and seizures. The clinical presentation is typically associated to mutations in the gene coding for the methyl-CpG-binding protein 2 ( MECP2 ), which is a transcription factor. The gene is ubiquitously present in all the cells of the organism with a peak of expression in neurons. For this re…
Biology (2 works) · Gene (2 works) · Computational biology (1 works) · Computer Science (1 works) · Data science (1 works) · DNA sequencing (1 works) · Evolutionary biology (1 works) · Gene expression (1 works) · Genetics (1 works) · Genetics (1 works)