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The Journal of Investigative Dermatology
|
February 24, 2016
Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
Nikolay V Zernov, Mikhail Y Skoblov, Andrey V Marakhonov, et al.
Bulletin of Experimental Biology and Medicine
|
September 4, 2022
Specific Antibodies to the Fragments of Meningococcal IgA1 Protease during the Formation of Immunity to Bacterial Infections
O V Kotel'nikova, Yu A Prokopenko, A A Zinchenko, et al.
Genetika
|
November 2, 2012
[Genetic epidemiological study of monogenic hereditary diseases in the Republic of Tatarstan: population dynamic factors determining the differentiation of the load of hereditary diseases in five districts]
E K Ginter, G I El'chinova, A N Petrin, et al.
International Journal of Molecular Sciences
|
November 25, 2023
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in <i>ABCA4</i>-Related Retinal Dystrophy in an Eastern European Population
Vitaly V Kadyshev, Ekaterina A Alekseeva, Vladimir V Strelnikov, et al.
Genetika
|
October 30, 2003
[Prevalence and molecular-genetic typing of nonsyndromal neurosensory deafness in the Chuvash Republic]
R A Zinchenko, S P Zinchenko, V A Galkina, et al.
Genetika
|
July 27, 2004
[Integrated population genetic and medical genetic study of two raions of the Tver oblast]
R A Zinchenko, G I El'chinova, G E Rudenskaia, et al.
Biosensors & Bioelectronics
|
March 31, 2012
Application of creatinine-sensitive biosensor for hemodialysis control
O A Zinchenko, S V Marchenko, T A Sergeyeva, et al.
International Journal of Molecular Sciences
|
November 14, 2023
Co-Occurrence of Congenital Aniridia Due to Nonsense <i>PAX6</i> Variant p.(Cys94*) and Chromosome 21 Trisomy in the Same Patient
Tatyana A Vasilyeva, Natella V Sukhanova, Andrey V Marakhonov, et al.
Genetika
|
July 19, 2007
[Population study of the Udmurt population: analysis of ten polymorphic DNA loci of the nuclear genome]
M A Bermisheva, N V Petrova, R A Zinchenko, et al.
Genetika
|
January 24, 2014
[MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic]
I M Khidiyatova, I A Skachkova, E V Saifullina, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 192) with videos related to
Sort By:
Page
of 20
The Journal of Investigative Dermatology
|
February 24, 2016
Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
Nikolay V Zernov, Mikhail Y Skoblov, Andrey V Marakhonov, et al.
Bulletin of Experimental Biology and Medicine
|
September 4, 2022
Specific Antibodies to the Fragments of Meningococcal IgA1 Protease during the Formation of Immunity to Bacterial Infections
O V Kotel'nikova, Yu A Prokopenko, A A Zinchenko, et al.
Genetika
|
November 2, 2012
[Genetic epidemiological study of monogenic hereditary diseases in the Republic of Tatarstan: population dynamic factors determining the differentiation of the load of hereditary diseases in five districts]
E K Ginter, G I El'chinova, A N Petrin, et al.
International Journal of Molecular Sciences
|
November 25, 2023
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in <i>ABCA4</i>-Related Retinal Dystrophy in an Eastern European Population
Vitaly V Kadyshev, Ekaterina A Alekseeva, Vladimir V Strelnikov, et al.
Genetika
|
October 30, 2003
[Prevalence and molecular-genetic typing of nonsyndromal neurosensory deafness in the Chuvash Republic]
R A Zinchenko, S P Zinchenko, V A Galkina, et al.
Genetika
|
July 27, 2004
[Integrated population genetic and medical genetic study of two raions of the Tver oblast]
R A Zinchenko, G I El'chinova, G E Rudenskaia, et al.
Biosensors & Bioelectronics
|
March 31, 2012
Application of creatinine-sensitive biosensor for hemodialysis control
O A Zinchenko, S V Marchenko, T A Sergeyeva, et al.
International Journal of Molecular Sciences
|
November 14, 2023
Co-Occurrence of Congenital Aniridia Due to Nonsense <i>PAX6</i> Variant p.(Cys94*) and Chromosome 21 Trisomy in the Same Patient
Tatyana A Vasilyeva, Natella V Sukhanova, Andrey V Marakhonov, et al.
Genetika
|
July 19, 2007
[Population study of the Udmurt population: analysis of ten polymorphic DNA loci of the nuclear genome]
M A Bermisheva, N V Petrova, R A Zinchenko, et al.
Genetika
|
January 24, 2014
[MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic]
I M Khidiyatova, I A Skachkova, E V Saifullina, et al.
Page
of 20