scispace - formally typeset
J

Julie A. Blendy

Researcher at German Cancer Research Center

Publications -  17
Citations -  4955

Julie A. Blendy is an academic researcher from German Cancer Research Center. The author has contributed to research in topics: CREB & Gene expression. The author has an hindex of 13, co-authored 17 publications receiving 4840 citations.

Papers
More filters
Journal ArticleDOI

Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein

TL;DR: Consistent with models claiming a role for long-term potentiation (LTP) in memory, LTP in hippocampal slices from CREB mutants decayed to baseline 90 min after tetanic stimulation, however, paired-pulse facilitation and posttetanic potentiation are normal.
Journal ArticleDOI

Targeted disruption of the glucocorticoid receptor gene blocks adrenergic chromaffin cell development and severely retards lung maturation

TL;DR: The results suggest that the adrenal medulla may be formed from two different cell populations: adrenergic-specific cells that require glucocorticoids for proliferation and/or survival, and a smaller noradrenergic population that differentiates normally in the absence of glucOCorticoid signaling.
Journal ArticleDOI

Severe impairment of spermatogenesis in mice lacking the CREM gene

TL;DR: The findings indicate that the CREM gene is essential for spermatogenesis, and mice deficient for this transcription factor could serve as a model system for the study of idiopathic infertility in men.
Journal ArticleDOI

Targeted mutation of the CREB gene: Compensation within the CREB/ATF family of transcription factors

TL;DR: It is demonstrated that CREB and two other members of the CREB/ATF family, cAMP response element modulation protein (CREM) and activating transcription factor 1 (ATF1), appear to form a unique subgroup within this extensive class of transcription factors.
Journal ArticleDOI

Spaced training induces normal long-term memory in CREB mutant mice.

TL;DR: It is demonstrated that CREB mutant mice have profound long-term memory deficits and manipulations of CREB function can affect the number of trials and the intertrial interval required for committing information to long- term memory.