about
Genomic analysis of the nuclear receptor family: new insights into structure, regulation, and evolution from the rat genomeDeletion of the cancer-amplified coactivator AIB3 results in defective placentation and embryonic lethalityEssential role of BETA2/NeuroD1 in development of the vestibular and auditory systemsAn allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.Genome-wide analysis of binding sites and direct target genes of the orphan nuclear receptor NR2F1/COUP-TFITuning of the outer hair cell motor by membrane cholesterol.DNA sequence analysis of SLC26A5, encoding prestin, in a patient-control cohort: identification of fourteen novel DNA sequence variationsHead bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness.Ablation of ghrelin receptor in leptin-deficient ob/ob mice has paradoxical effects on glucose homeostasis when compared with ablation of ghrelin in ob/ob mice.Dielectric properties of yeast cells expressed with the motor protein prestinAssessment of prestin self-association using fluorescence resonance energy transfer.Sensorineural hearing loss: potential therapies and gene targets for drug development.An Atoh1-S193A phospho-mutant allele causes hearing deficits and motor impairment.Membrane prestin expression correlates with the magnitude of prestin-associated charge movement.Loss of orphan receptor germ cell nuclear factor function results in ectopic development of the tail bud and a novel posterior truncation.Membrane composition modulates prestin-associated charge movement.Functional prestin transduction of immature outer hair cells from normal and prestin-null mice.Effects of prestin on membrane mechanics and electromechanics.Chicken ovalbumin upstream promoter-transcription factors and their regulation.Selective cell-surface labeling of the molecular motor protein prestinGlycosylation regulates prestin cellular activity.Dynamic expression of COUP-TFI and COUP-TFII during development and functional maturation of the mouse inner ear.The 56 kDa androgen-binding protein in human genital skin fibroblasts: its relation to the human androgen receptor.Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindredPresenilins are required for the formation of comma- and S-shaped bodies during nephrogenesis
P50
Q24598049-E88F3649-7F06-4E16-AC88-A2CAA45F08D7Q28507924-AB347000-C0DE-488D-828B-47D1E7A2756FQ29026493-8C23E34E-1235-49E3-B2A1-91D7A101B73EQ30457871-6B37469B-37ED-4DBE-A6DF-AE08F8E7E851Q30483743-3CC1C48B-2BD5-49C8-82D4-0272F375B60EQ30487502-E15BFA57-4382-46F5-A14C-72650A9AE0EDQ33459170-CB32C7A8-7492-4B5B-84F9-0BD206071A7CQ35942220-7345410C-D89C-4665-915F-B7D007F61BD5Q36176019-E541D148-19AC-4ED8-A4C5-EDBE09BC4328Q36273795-753FEF84-0DFF-4F80-81EA-912E2A3FA142Q36454437-B5B86FFE-09B7-4253-9C9E-EAEEB854DD22Q36604532-7FFC1D45-9D91-4023-9162-8A69E3D47AEAQ38669117-44EB33DF-9347-41D6-950C-017C8C8F2469Q38766524-9B269CA6-CD4B-4D4E-A2A3-F1453C9A9DB9Q39457575-76379D63-33A6-4F01-8CD7-4BCE7E92E492Q39970141-B69E6120-0E52-444B-9DB8-6B3BD615785CQ39978159-62893072-F850-46ED-9A23-1D4DDB151B90Q40052024-54D326CC-8B86-4969-97BF-6FC86953ACC5Q40971221-16714416-411E-4966-8D84-2CE7DD20FED8Q41815570-0F31E438-8B04-4C6F-8540-D1A9A9CCA1E5Q42029796-0454B54D-3E88-4503-B96C-F66CE50C4FB4Q52049244-D7A2D514-9FC6-4F76-A4E3-0F3DCB63BBDEQ54332143-12DD7358-25F5-4C33-812A-071D95EBCE63Q71690087-415B44DC-73FF-46AA-83ED-82B16DEE8AE4Q73833078-0AA52327-176E-4AFB-89A6-505D72AA0513
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fred A Pereira
@nl
Fred A Pereira
@sl
Fred A. Pereira
@en
Fred A. Pereira
@es
type
label
Fred A Pereira
@nl
Fred A Pereira
@sl
Fred A. Pereira
@en
Fred A. Pereira
@es
prefLabel
Fred A Pereira
@nl
Fred A Pereira
@sl
Fred A. Pereira
@en
Fred A. Pereira
@es
P106
P1153
7201690319
P21
P31
P496
0000-0003-2100-0280