21 results on '"Slc26a4"'
Search Results
2. Novel functions of the anion exchanger AE4 (SLC4A9)
3. Identification of potential susceptibility genes in patients with primary Sjögren’s syndrome-associated pulmonary arterial hypertension through whole exome sequencing
4. Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss
5. Compound heterozygous variants of the SLC26A4 gene in a Chinese family with enlarged vestibular aqueducts
6. A newly identified mutation (c.2029 C > T) in SLC26A4 gene is associated with enlarged vestibular aqueducts in a Chinese family
7. SLC26A4 correlates with homologous recombination deficiency and patient prognosis in prostate cancer
8. A case of Landau-Kleffner syndrome with SLC26A4-related hearing impairment
9. Cochlear Pathomorphogenesis of Incomplete Partition Type II in Slc26a4-Null Mice
10. Identification and computational analysis of USH1C, and SLC26A4 variants in Pakistani families with prelingual hearing loss
11. A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns
12. Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India
13. Acute regulated expression of pendrin in human urinary exosomes
14. Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
15. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects
16. Hereditäre Schwerhörigkeit: Teil 1: Überblick und praktische Hinweise zur Diagnostik
17. Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet
18. Pendred syndrome among patients with congenital hypothyroidism detected by neonatalscreening: identification of two novel PDS/SLC26A4 mutations
19. Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct
20. Distribution of pendrin in the organ of Corti of mice observed by electron immunomicroscopy
21. Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct
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