Surin V - Search Results

1

Atlas of RNA sequencing profiles for normal human tissues.

Suntsova M, Gaifullin N, Allina D, Reshetun A, Li X, Mendeleeva L, Surin V, Sergeeva A, Spirin P, Prassolov V, Morgan A, Garazha A, Sorokin M, Buzdin A. Suntsova M, et al. Among authors: surin v. Sci Data. 2019 Apr 23;6(1):36. doi: 10.1038/s41597-019-0043-4. Sci Data. 2019. PMID: 31015567 Free PMC article.

2

[Hereditary afibrinogenemia: A literature review and clinical observations].

Yakovleva EV, Surin VL, Selivanova DS, Sergeeva AM, Gonсharova MV, Demidova EY, Soboleva NP, Makhinya SA, Dezhenkova AV, Likhacheva EA, Zozulya NI. Yakovleva EV, et al. Among authors: surin vl. Ter Arkh. 2016;88(12):120-125. doi: 10.17116/terarkh20168812120-125. Ter Arkh. 2016. PMID: 28635887 Review. Russian.

3

Machine Learning Applicability for Classification of PAD/VCD Chemotherapy Response Using 53 Multiple Myeloma RNA Sequencing Profiles.

Borisov N, Sergeeva A, Suntsova M, Raevskiy M, Gaifullin N, Mendeleeva L, Gudkov A, Nareiko M, Garazha A, Tkachev V, Li X, Sorokin M, Surin V, Buzdin A. Borisov N, et al. Among authors: surin v. Front Oncol. 2021 Apr 15;11:652063. doi: 10.3389/fonc.2021.652063. eCollection 2021. Front Oncol. 2021. PMID: 33937058 Free PMC article.

4

[Amplification of hypervariable genomic regions for establishment of the type of hematopoiesis in hemoblastosis patients after allogeneic bone marrow transplantation].

Demidova IA, Surin VL, Mendeleeva LP, Savchenko VG. Demidova IA, et al. Among authors: surin vl. Genetika. 1997 Apr;33(4):546-9. Genetika. 1997. PMID: 9206670 Clinical Trial. Russian.

5

[No title available]

[No authors listed] [No authors listed] PMID: 36164082

6

[Li-Fraumeni syndrome in adult patients with acute lymphoblastic leukemia].

Zarubina KI, Parovichnikova EN, Surin VL, Pshenichnikova OS, Gavrilina OA, Isinova GA, Troitskaya VV, Sokolov AN, Galtseva IV, Kapranov NM, Davydova JO, Obukhova TN, Nikulina EE, Sudarikov AB, Savchenko VG. Zarubina KI, et al. Among authors: surin vl. Ter Arkh. 2021 Jul 23;93(7):763-769. doi: 10.26442/00403660.2021.07.200913. Ter Arkh. 2021. PMID: 36286726 Russian.

7

Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert's syndrome.

Petrenko AA, Pivnik AV, Kim PP, Demidova EY, Surin VL, Abdullaev AO, Sudarikov AB, Petrova NA, Maryina SA. Petrenko AA, et al. Among authors: surin vl. Ter Arkh. 2018 Aug 17;90(7):105-109. doi: 10.26442/terarkh2018907105-109. Ter Arkh. 2018. PMID: 30701931

8

Literature review and clinical observation of acquired idiopathic hemophilia with a new missense mutation in the factor VIII gene (His2026Arg).

Ershov VI, Gadaev IY, Perina FG, Surin VL, Salomashkina VV, Pshenichnikova OS, Zozulya NI. Ershov VI, et al. Among authors: surin vl. Ter Arkh. 2018 Aug 17;90(7):118-122. doi: 10.26442/terarkh2018907118-122. Ter Arkh. 2018. PMID: 30701933 Review.

9

[Allogenic bone marrow transplantation after reduced intensity conditioning regimens in therapy of patients with hemoblastoses].

Demidova IA, Savchenko VG, Ol'shanskaia IuV, Poreshina LP, Kut'ina RM, Surin VL, Misiurin AV, Domracheva EV, Parovichnikova EN. Demidova IA, et al. Among authors: surin vl. Ter Arkh. 2003;75(7):15-21. Ter Arkh. 2003. PMID: 12934475 Russian.

10

[Molecular genetic study of acute intermittent porphyria in Russia: mutation analysis and functional polymorphism search in porphobilinogen deaminase gene].

Surin VL, Luchinina IuA, Selivanova DS, Pustovoĭt IaS, Karpova IS, Pivnik AV, Luk'ianenko AV, Kravchenko SK. Surin VL, et al. Genetika. 2010 Apr;46(4):540-52. Genetika. 2010. PMID: 20536026 Russian.

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