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Human Molecular Genetics
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June 22, 2000
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice
E V Semina, J C Murray, R Reiter, et al.
Genetika
|
October 1, 1993
[Family analysis of human "fingerprints" obtained using a phage M13 DNA probe]
E V Semina (Barysheva), A M Bukina, E K Ginter, et al.
Human Molecular Genetics
|
June 9, 1998
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome
S C Kulak, K Kozlowski, E V Semina, et al.
Human Molecular Genetics
|
February 13, 2001
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
E V Semina, I Brownell, H A Mintz-Hittner, et al.
Clinical Genetics
|
March 18, 2014
Whole exome analysis identifies dominant COL4A1 mutations in patients with complex ocular phenotypes involving microphthalmia
B Deml, L M Reis, M Maheshwari, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
February 27, 2023
[An analysis of the relationship between genetic factors and the risk of schizophrenia]
A A Shmakova, E V Semina, E A Neyfeld, et al.
Arkhiv Patologii
|
February 26, 2020
[Cancer-associated fibroblasts and their significance in tumor progression]
N A Oleynikova, N V Danilova, I A Mikhailov, et al.
Genetika
|
October 1, 1993
[Genetic distances between various ethnic populations calculated on the basis of polymorphism of DNA detected by the hypervariable phage M13 DNA probe]
E V Semina (Barysheva), A M Bukina, E A Startseva, et al.
European Journal of Human Genetics : EJHG
|
October 22, 1998
Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene
H el-Shanti, J C Murray, E V Semina, et al.
European Journal of Cell Biology
|
November 19, 2021
Revisiting the multiple roles of T-cadherin in health and disease
K A Rubina, E V Semina, N I Kalinina, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Human Molecular Genetics
|
June 22, 2000
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice
E V Semina, J C Murray, R Reiter, et al.
Genetika
|
October 1, 1993
[Family analysis of human "fingerprints" obtained using a phage M13 DNA probe]
E V Semina (Barysheva), A M Bukina, E K Ginter, et al.
Human Molecular Genetics
|
June 9, 1998
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome
S C Kulak, K Kozlowski, E V Semina, et al.
Human Molecular Genetics
|
February 13, 2001
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
E V Semina, I Brownell, H A Mintz-Hittner, et al.
Clinical Genetics
|
March 18, 2014
Whole exome analysis identifies dominant COL4A1 mutations in patients with complex ocular phenotypes involving microphthalmia
B Deml, L M Reis, M Maheshwari, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
February 27, 2023
[An analysis of the relationship between genetic factors and the risk of schizophrenia]
A A Shmakova, E V Semina, E A Neyfeld, et al.
Arkhiv Patologii
|
February 26, 2020
[Cancer-associated fibroblasts and their significance in tumor progression]
N A Oleynikova, N V Danilova, I A Mikhailov, et al.
Genetika
|
October 1, 1993
[Genetic distances between various ethnic populations calculated on the basis of polymorphism of DNA detected by the hypervariable phage M13 DNA probe]
E V Semina (Barysheva), A M Bukina, E A Startseva, et al.
European Journal of Human Genetics : EJHG
|
October 22, 1998
Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene
H el-Shanti, J C Murray, E V Semina, et al.
European Journal of Cell Biology
|
November 19, 2021
Revisiting the multiple roles of T-cadherin in health and disease
K A Rubina, E V Semina, N I Kalinina, et al.
Page
of 5