Suchergebnisse - "Carpinelli, Marina R"

PubPharm (31)

1

Grainyhead-like 2 interacts with noggin to regulate tissue fusion in mouse

enthalten in: Development (Cambridge, England) | 2024

von de Vries, M. | Carpinelli, M. | Fuller, J. | +6

2

Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects

enthalten in: Developmental dynamics : an official publication of the American Association of Anatomists | 2023

von Deng, Z. | Butt, T. | Arhatari, B. | +9

3

Inhibition of retinoic acid signaling impairs cranial and spinal neural tube closure in mice lacking the Grainyhead-like 3 transcription factor

enthalten in: Biochemical and biophysical research communications | 2022

von Deng, Z. | Carpinelli, M. | Butt, T. | +3

4

Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects

enthalten in: ResearchSquare.com | 2022

von Deng, Z. | Butt, T. | Arhatari, B. | +9

5

Grainyhead-like transcription factors : guardians of the skin barrier

enthalten in: Veterinary dermatology | 2021

von Deng, Z. | Cangkrama, M. | Butt, T. | +2

6

Delineating the roles of Grhl2 in craniofacial development through tissue-specific conditional deletion and epistasis approaches in mouse

enthalten in: Developmental dynamics : an official publication of the American Association of Anatomists | 2021

von de Vries, M. | Owens, H. | Carpinelli, M. | +7

7

Delineating the roles of Grhl2 in craniofacial development through tissue‐specific conditional deletion and epistasis approaches in mouse

enthalten in: Developmental Dynamics | 2021

von Vries, M. | Owens, H. | Carpinelli, M. | +7

8

Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure

enthalten in: Disease models & mechanisms | 2020

von Carpinelli, M. | de Vries, M. | Auden, A. | +12

9

Stage-dependent therapeutic efficacy in PI3K/mTOR-driven squamous cell carcinoma of the skin

enthalten in: Cell death and differentiation | 2018

von Darido, C. | Georgy, S. | Cullinane, C. | +8

10

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

enthalten in: Scientific reports | 2018

von Ogier, J. | Arhatari, B. | Carpinelli, M. | +3