Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Filter bei nächster Suche beibehalten
topic_facet:"SLC26A4 protein, human"
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22YUAN+HUIJUN%22&type=Person&filter%5B%5D=topic_facet%3A%22SLC26A4+protein%2C+human%22
/vufind/Search/Results?lookfor=%22YUAN+HUIJUN%22&type=Person&filter%5B%5D=topic_facet%3A%22SLC26A4+protein%2C+human%22
Search /vufind/Search2/Results?lookfor=%22YUAN+HUIJUN%22&type=Person&filter%5B%5D=topic_facet%3A%22SLC26A4+protein%2C+human%22
PubPharm (9)
1
A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss
enthalten in:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
| 2016
von
Zhang, D.
|
Duan, H.
|
Lin, P.
| +9
Wird geladen...
2
Application of SNPscan in Genetic Screening for Common Hearing Loss Genes
enthalten in:
PloS one
| 2016
von
Gao, Z.
|
Lu, Y.
|
Ke, J.
| +10
Wird geladen...
3
Resolving the genetic heterogeneity of prelingual hearing loss within one family : Performance comparison and application of two targeted next generation sequencing approaches
enthalten in:
Journal of human genetics
| 2014
von
Lu, Y.
|
Zhou, X.
|
Jin, Z.
| +10
Wird geladen...
4
A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss
enthalten in:
Genomics
| 2014
von
Du, W.
|
Cheng, J.
|
Ding, H.
| +3
Wird geladen...
5
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China
enthalten in:
Journal of translational medicine
| 2009
von
Yuan, Y.
|
You, Y.
|
Huang, D.
| +8
Wird geladen...
6
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss
enthalten in:
Physiological genomics
| 2009
von
Dai, P.
|
Stewart, A.
|
Chebib, F.
| +19
ErratumIn: Physiol Genomics. 2010 Feb;40(3):216
Wird geladen...
7
Molecular etiology of hearing impairment in Inner Mongolia : mutations in SLC26A4 gene and relevant phenotype analysis
enthalten in:
Journal of translational medicine
| 2008
von
Dai, P.
|
Yuan, Y.
|
Huang, D.
| +7
Wird geladen...
8
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2008
von
Dai, P.
|
Li, Q.
|
Huang, D.
| +13
Wird geladen...
9
Genotypic analysis of familial dilated vestibular aqueduct syndrome
enthalten in:
Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
| 2006
von
Dai, P.
|
Han, D.
|
Cao, J.
| +10
Wird geladen...
1
[1]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Ihre gewählten Filter
Filter bei nächster Suche beibehalten
Filter aufheben
Thema: SLC26A4 protein, human
Medienart
9
Aufsätze
8
E-Artikel
8
E-Ressourcen
1
Gedruckte Aufsätze
Zeitschriftentitel
2
Journal of translational medicine
1
Genetics in medicine : official journal of the ...
1
Genomics
1
Journal of human genetics
1
Lin chuang er bi yan hou ke za zhi = Journal of...
1
Physiological genomics
1
PloS one
1
Zhonghua er bi yan hou tou jing wai ke za zhi =...
Alle anzeigen ...
weniger ...
Thema
9
Journal Article
9
Membrane Transport Proteins
SLC26A4 protein, human
9
Sulfate Transporters
7
Research Support, Non-U.S. Gov't
6
127120-53-0
6
Connexin 26
6
Connexins
6
GJB2 protein, human
4
RNA, Ribosomal
4
RNA, ribosomal, 12S
2
DNA, Mitochondrial
2
Thyroid Hormones
1
CDH23 protein, human
1
Cadherin Related Proteins
1
Cadherins
1
Chlorides
1
Comparative Study
1
GJB2
1
Gene mutation
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
4
2010-2019
5
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
7
Englisch
2
Chinesisch
Haven't found what you're looking for?
Wird geladen...