| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult neurogenesis: Is it showtime for clinical translation?
|
Lai, Yu-Jie
|
|
2015
|
2 |
4 |
p. 291-292
2 p.
|
artikel
|
| 2 |
Authentication of experimental materials: A remedy for the reproducibility crisis?
|
Li, Fei
|
|
2015
|
2 |
4 |
p. 283-
1 p.
|
artikel
|
| 3 |
Chondrogenic priming of human fetal synovium-derived stem cells in an adult stem cell matrix microenvironment
|
Li, Jingting
|
|
2015
|
2 |
4 |
p. 337-346
10 p.
|
artikel
|
| 4 |
Corrigendum to ‘Bmi-1: At the crossroads of physiological and pathological biology’ [Genes & Diseases 2 (2015) 225–239]
|
Bhattacharya, Resham
|
|
2015
|
2 |
4 |
p. 353-
1 p.
|
artikel
|
| 5 |
CRISPR comes of age: A fairytale turned into bedside reality?
|
Li, Fei
|
|
2015
|
2 |
4 |
p. 284-285
2 p.
|
artikel
|
| 6 |
Damage control: Harnessing prostaglandin E2 as a potential healing factor of tissue injuries
|
Shao, Connie
|
|
2015
|
2 |
4 |
p. 295-298
4 p.
|
artikel
|
| 7 |
Direct lineage conversion with pluripotency factors: A risky detour through transient pluripotency?
|
Li, Fei
|
|
2015
|
2 |
4 |
p. 286-287
2 p.
|
artikel
|
| 8 |
For your eyes only: Harnessing human embryonic stem cell-derived retinal pigment epithelial cells to improve impaired vision
|
Hu, Jim
|
|
2015
|
2 |
4 |
p. 293-294
2 p.
|
artikel
|
| 9 |
Multifaceted signaling regulators of chondrogenesis: Implications in cartilage regeneration and tissue engineering
|
Green, Jordan D.
|
|
2015
|
2 |
4 |
p. 307-327
21 p.
|
artikel
|
| 10 |
Opening the LOX to bone metastasis: The role of secreted lysyl oxidase in skeletal recurrence of breast cancers
|
Mohammed, Maryam K.
|
|
2015
|
2 |
4 |
p. 288-290
3 p.
|
artikel
|
| 11 |
Promising molecular mechanisms responsible for gemcitabine resistance in cancer
|
Jia, Yanfei
|
|
2015
|
2 |
4 |
p. 299-306
8 p.
|
artikel
|
| 12 |
Skeletal muscle as an endocrine organ: Role of [Na+]i/[K+]i-mediated excitation-transcription coupling
|
Kapilevich, Leonid V.
|
|
2015
|
2 |
4 |
p. 328-336
9 p.
|
artikel
|
| 13 |
Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2
|
Lyon, Sarah M.
|
|
2015
|
2 |
4 |
p. 347-352
6 p.
|
artikel
|
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