Sequence variations in CREB1 cosegregate with depressive disorders in women (Q73637501)

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5 November 2019

title

Sequence variations in CREB1 cosegregate with depressive disorders in women (English)

1 reference

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5 November 2019

author name string

Zubenko GS

1

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5 November 2019

Hughes HB 3rd

2

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5 November 2019

Stiffler JS

3

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5 November 2019

Brechbiel A

4

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5 November 2019

Zubenko WN

5

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5 November 2019

Maher BS

6

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5 November 2019

Marazita ML

7

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5 November 2019

publication date

1 June 2003

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5 November 2019

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5 November 2019

volume

8

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5 November 2019

issue

6

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5 November 2019

page(s)

611-618

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Malignancy of recurrent, early-onset major depression: a family study

5 November 2019

cites work

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Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression

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Transcriptional regulation by the phosphorylation-dependent factor CREB

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Involvement of cyclic AMP response element binding protein (CREB) and estrogen receptor phosphorylation in the synergistic activation of the estrogen receptor by estradiol and protein kinase activators

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D2S2944 identifies a likely susceptibility locus for recurrent, early-onset, major depression in women

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7 January 2021

Construction of multilocus genetic linkage maps in humans

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7 January 2021

A general conditional-logistic model for affected-relative-pair linkage studies

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7 January 2021

Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4.

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7 January 2021

Comprehensive human genetic maps: individual and sex-specific variation in recombination

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7 January 2021

The promoter of the gene encoding 3',5'-cyclic adenosine monophosphate (cAMP) response element binding protein contains cAMP response elements: evidence for positive autoregulation of gene transcription

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7 January 2021

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Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein-Taybi syndrome

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7 January 2021

Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001354

1 reference

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5 November 2019

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