Pendrin function in airway epithelia.

Charity Nofziger; Silvia Dossena; Shoichi Suzuki; Kenji Izuhara; Markus Paulmichl

doi:10.1159/000335115

Pendrin function in airway epithelia.

Charity Nofziger (First author)
, Silvia Dossena (Co-author)
, Shoichi Suzuki
, Kenji Izuhara
, Markus Paulmichl^* (Last author)

^*Corresponding author for this work

Institute of Pharmacology and Toxicology

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

36 Citations (Web of Science)

Original language	English
Pages (from-to)	571-578
Journal	Cellular physiology and biochemistry
Volume	28
Issue number	3
DOIs	https://doi.org/10.1159/000335115
Publication status	Published - 2011

Keywords

OBSTRUCTIVE PULMONARY-DISEASE
SYNDROME GENE
BRONCHIAL-ASTHMA
SERUM LEVELS
INNER-EAR
INTERFERON-GAMMA
MUCUS PRODUCTION
NA+/I-SYMPORTER
ION-TRANSPORT
EXPRESSION

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10.1159/000335115

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{d952353e35504763a8362180c39e10cd,

title = "Pendrin function in airway epithelia.",

keywords = "OBSTRUCTIVE PULMONARY-DISEASE, SYNDROME GENE, BRONCHIAL-ASTHMA, SERUM LEVELS, INNER-EAR, INTERFERON-GAMMA, MUCUS PRODUCTION, NA+/I-SYMPORTER, ION-TRANSPORT, EXPRESSION",

author = "Charity Nofziger and Silvia Dossena and Shoichi Suzuki and Kenji Izuhara and Markus Paulmichl",

note = "Institute of Pharmacology and Toxicology, Paracelsus Medical University, Salzburg, ",

year = "2011",

doi = "10.1159/000335115",

language = "English",

volume = "28",

pages = "571--578",

journal = "Cellular physiology and biochemistry",

issn = "1015-8987",

number = "3",

}

TY - JOUR

T1 - Pendrin function in airway epithelia.

AU - Nofziger, Charity

AU - Dossena, Silvia

AU - Suzuki, Shoichi

AU - Izuhara, Kenji

AU - Paulmichl, Markus

N1 - Institute of Pharmacology and Toxicology, Paracelsus Medical University, Salzburg,

PY - 2011

Y1 - 2011

KW - OBSTRUCTIVE PULMONARY-DISEASE

KW - SYNDROME GENE

KW - BRONCHIAL-ASTHMA

KW - SERUM LEVELS

KW - INNER-EAR

KW - INTERFERON-GAMMA

KW - MUCUS PRODUCTION

KW - NA+/I-SYMPORTER

KW - ION-TRANSPORT

KW - EXPRESSION

U2 - 10.1159/000335115

DO - 10.1159/000335115

M3 - Review article

C2 - 22116372

SN - 1015-8987

VL - 28

SP - 571

EP - 578

JO - Cellular physiology and biochemistry

JF - Cellular physiology and biochemistry

IS - 3

ER -

Pendrin function in airway epithelia.

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