The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".

Silvia Dossena; Charity Nofziger; Florian Lang; Giovanna Valenti; Markus Paulmichl

doi:10.1159/000335101

The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".

Silvia Dossena (First author)
, Charity Nofziger (Co-author)
, Florian Lang
, Giovanna Valenti
, Markus Paulmichl^* (Last author)

^*Corresponding author for this work

Institute of Pharmacology and Toxicology

Research output: Contribution to journal › Review article › peer-review

9 Citations (Web of Science)

Original language	English
Pages (from-to)	377-384
Journal	Cellular physiology and biochemistry
Volume	28
Issue number	3
DOIs	https://doi.org/10.1159/000335101
Publication status	Published - 2011

Keywords

OBSTRUCTIVE PULMONARY-DISEASE
SYNDROME GENE PDS
INNER-EAR
BICARBONATE SECRETION
IODIDE TRANSPORT
NA+/I-SYMPORTER
HEARING-LOSS
WILD-TYPE
SLC26A4
EXPRESSION

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10.1159/000335101

Transcriptional regulation of SLC24A4 (pendrin), a protein causing Pendred-Syndrome, a human hereditary disease associated with deafness and goiter
Paulmichl, M. (PI)
19/02/10 → 18/02/12
Project: Research

Cite this

@article{eba6e1460e864fe780d0fcabc6c98fef,

title = "The ESF meeting on {"}The proteomics, epigenetics and pharmacogenetics of pendrin{"}.",

keywords = "OBSTRUCTIVE PULMONARY-DISEASE, SYNDROME GENE PDS, INNER-EAR, BICARBONATE SECRETION, IODIDE TRANSPORT, NA+/I-SYMPORTER, HEARING-LOSS, WILD-TYPE, SLC26A4, EXPRESSION",

author = "Silvia Dossena and Charity Nofziger and Florian Lang and Giovanna Valenti and Markus Paulmichl",

year = "2011",

doi = "10.1159/000335101",

language = "English",

volume = "28",

pages = "377--384",

journal = "Cellular physiology and biochemistry",

issn = "1015-8987",

number = "3",

}

TY - JOUR

T1 - The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".

AU - Dossena, Silvia

AU - Nofziger, Charity

AU - Lang, Florian

AU - Valenti, Giovanna

AU - Paulmichl, Markus

PY - 2011

Y1 - 2011

KW - OBSTRUCTIVE PULMONARY-DISEASE

KW - SYNDROME GENE PDS

KW - INNER-EAR

KW - BICARBONATE SECRETION

KW - IODIDE TRANSPORT

KW - NA+/I-SYMPORTER

KW - HEARING-LOSS

KW - WILD-TYPE

KW - SLC26A4

KW - EXPRESSION

U2 - 10.1159/000335101

DO - 10.1159/000335101

M3 - Review article

C2 - 22116352

SN - 1015-8987

VL - 28

SP - 377

EP - 384

JO - Cellular physiology and biochemistry

JF - Cellular physiology and biochemistry

IS - 3

ER -

The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".

Keywords

Access to Document

Projects

Transcriptional regulation of SLC24A4 (pendrin), a protein causing Pendred-Syndrome, a human hereditary disease associated with deafness and goiter

Cite this