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1.
A Systematic Review and Meta-Analysis of Free Triiodothyronine (FT3) Levels in Humans Depending on Seasonal Air Temperature Changes: Is the Variation in FT3 Levels Related to Nonshivering Thermogenesis?
Int J Mol Sci
; 24(18)2023 Sep 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-37762355
2.
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
Hum Genet
; 141(3-4): 697-707, 2022 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-34839402
3.
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies
Int J Mol Sci
; 23(23)2022 Dec 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36499699
4.
The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia.
Int J Mol Sci
; 22(9)2021 Apr 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-33925025
5.
The limitations of kinship determinations using STR data in ill-defined populations.
Int J Legal Med
; 134(6): 1981-1990, 2020 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-32318826
6.
Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).
ScientificWorldJournal
; 2019: 5198931, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31015822
7.
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
BMC Med Genet
; 19(1): 138, 2018 08 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-30086704
8.
The genetic legacy of the expansion of Turkic-speaking nomads across Eurasia.
PLoS Genet
; 11(4): e1005068, 2015 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25898006
9.
Perylene Derivative Dyes Luminescence in Polysiloxane Matrix in Presence of Gold Nanoparticles.
J Fluoresc
; 26(6): 2213-2223, 2016 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-27592354
10.
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).
Genes (Basel)
; 14(5)2023 04 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37239361
11.
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.
Biology (Basel)
; 11(2)2022 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35205123
12.
Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia.
Genes (Basel)
; 13(9)2022 09 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36140780
13.
Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect.
J Hum Genet
; 56(9): 631-9, 2011 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-21776002
14.
Study of the effect of the introduction of Tris(bipyridine)ruthenium(II) chloride into silicon dioxide particles by spectrofluorometry methods.
Spectrochim Acta A Mol Biomol Spectrosc
; 246: 119007, 2021 Feb 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33065450
15.
Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
Diagnostics (Basel)
; 11(12)2021 Dec 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-34943614
16.
The attitude of young people in the city of Yakutsk to DNA-testing.
Int J Circumpolar Health
; 80(1): 1973697, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34544327
17.
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.
Eur J Hum Genet
; 29(6): 965-976, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33767456
18.
Fluorescent chemosensor for detection and quantitation of carbon dioxide gas.
J Am Chem Soc
; 132(40): 13951-3, 2010 Oct 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-20853831
19.
Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.
J Hum Genet
; 55(11): 749-54, 2010 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-20739944
20.
High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect.
Genes (Basel)
; 11(7)2020 07 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-32708339