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Showing 1 to 12 of 30 entries
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New insights into the management of rhythm and conduction disorders after acute myocardial infarction.

The American journal of case reports

Korostovtseva L, Sviryaev Y, Zvartau N, Druzhkova T, Tikhonenko V, Konradi A.
PMID: 24782917
Am J Case Rep. 2014 Apr 19;15:159-62. doi: 10.12659/AJCR.890357. eCollection 2014.

PATIENT: Male, 53 FINAL DIAGNOSIS: Myocardial infarction Symptoms: Chest pain • tachycardiaMEDICATION: - Clinical Procedure: - Specialty: Cardiology.OBJECTIVE: Challenging differential diagnosis.BACKGROUND: Comorbidities, including obesity and sleep-breathing disorders, can adversely influence outcomes in acute myocardial infarction (AMI), and should be...

Ytterbocenes as one- and two-electron reductants in their reactions with diazadienes: YbIII mixed-ligand bent-sandwich complexes containing a dianion of diazabutadiene.

Chemistry (Weinheim an der Bergstrasse, Germany)

Trifonov AA, Borovkov IA, Fedorova EA, Fukin GK, Larionova J, Druzhkov NO, Cherkasov VK.
PMID: 17366494
Chemistry. 2007;13(17):4981-7. doi: 10.1002/chem.200601481.

Ytterbocene [Yb(C(5)MeH(4))(2)(thf)(2)] reacts with diazabutadiene 2,6-iPr(2)C(6)H(3)-N=CH-CH=N-C(6)H(3)iPr(2)-2,6 (DAD) as a one-electron reductant to afford a bis(cyclopentadienyl) Yb(III) derivative containing a DAD radical anion [Yb(C(5)MeH(4))(2)(dad(-.))]. However, ytterbocenes [YbCp*(2)(thf)(2)] (Cp*=C(5)Me(5), C(5)Me(4)H) coordinated by sterically demanding cyclopentadienyl ligands act as two-electron reductants in...

Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome.

Journal of autism and developmental disorders

Beskorovainaya T, Konovalov F, Demina N, Shchagina O, Pashchenko M, Kanivets I, Pyankov D, Ryzhkova O, Polyakov A.
PMID: 32816169
J Autism Dev Disord. 2021 Jun;51(6):2159-2163. doi: 10.1007/s10803-020-04668-0.

No abstract available.

The Role of Plasma Membrane Viscosity in the Response and Resistance of Cancer Cells to Oxaliplatin.

Cancers

Shimolina L, Gulin A, Ignatova N, Druzhkova I, Gubina M, Lukina M, Snopova L, Zagaynova E, Kuimova MK, Shirmanova M.
PMID: 34944789
Cancers (Basel). 2021 Dec 07;13(24). doi: 10.3390/cancers13246165.

Maintenance of the biophysical properties of membranes is essential for cell survival upon external perturbations. However, the links between a fluid membrane state and the drug resistance of cancer cells remain elusive. Here, we investigated the role of membrane...

Complete mitochondrial genome of an extinct .

Mitochondrial DNA. Part B, Resources

Druzhkova AS, Makunin AI, Vorobieva NV, Vasiliev SK, Ovodov ND, Shunkov MV, Trifonov VA, Graphodatsky AS.
PMID: 33473722
Mitochondrial DNA B Resour. 2017 Feb 06;2(1):79-81. doi: 10.1080/23802359.2017.1285209.

No abstract available.

Tracing of intracellular pH in cancer cells in response to Taxol treatment.

Cell cycle (Georgetown, Tex.)

Druzhkova I, Lukina M, Dudenkova V, Ignatova N, Snopova L, Gavrina A, Shimolina L, Belousov V, Zagaynova E, Shirmanova M.
PMID: 34308742
Cell Cycle. 2021 Aug;20(16):1540-1551. doi: 10.1080/15384101.2021.1949106. Epub 2021 Jul 25.

Genetically encoded pH-sensors are the promising instrument for intracellular pH (pHi) registration. In tumor tissue the reversed pH gradient is known to be the important hallmark of cancer and regulator of tumor response on chemotherapy. However the effect of...

Novel Compound Heterozygous Variants in the .

The application of clinical genetics

Zabnenkova V, Shchagina O, Makienko O, Matyushchenko G, Ryzhkova O.
PMID: 35023948
Appl Clin Genet. 2022 Jan 06;15:1-10. doi: 10.2147/TACG.S342804. eCollection 2022.

BACKGROUND: Meier-Gorlin syndrome (MGS) is a rare genetic syndrome inherited in an autosomal dominant or autosomal recessive manner. The disorder is characterized by bilateral microtia, absence or hypoplasia of the patella, and an intrauterine growth retardation as well as...

Next Generation Sequencing of Chromosome-Specific Libraries Sheds Light on Genome Evolution in Paleotetraploid Sterlet (Acipenser ruthenus).

Genes

Andreyushkova DA, Makunin AI, Beklemisheva VR, Romanenko SA, Druzhkova AS, Biltueva LB, Serdyukova NA, Graphodatsky AS, Trifonov VA.
PMID: 29125582
Genes (Basel). 2017 Nov 10;8(11). doi: 10.3390/genes8110318.

Several whole genome duplication (WGD) events followed by rediploidization took place in the evolutionary history of vertebrates. Acipenserids represent a convenient model group for investigation of the consequences of WGD as their representatives underwent additional WGD events in different...

Asymmetric Dimethylarginine in Patients with Ascending Aortic Aneurysms.

Aorta (Stamford, Conn.)

Gavriliuk ND, Druzhkova TA, Irtyuga OB, Zhloba AA, Subbotina TF, Uspenskiy VE, Alexeyeva NP, Moiseeva OM.
PMID: 28516097
Aorta (Stamford). 2016 Dec 01;4(6):219-225. doi: 10.12945/j.aorta.2016.16.025. eCollection 2016 Dec.

BACKGROUND: Ascending thoracic aortic aneurysm (aTAA) is a heterogeneous group of disorders that involve impaired endothelial function. The nitric oxide (NO) synthase inhibitor asymmetric dimethylarginine (ADMA) serves as an endothelial dysfunction marker. Thus, we investigated ADMA levels in patients...

Stress load and neurodegeneration after gastrostomy tube placement in amyotrophic lateral sclerosis patients.

Metabolic brain disease

Brylev L, Fominykh V, Chernenkaia V, Chernenkiy I, Gorbachev K, Ataulina A, Izvekov A, Monakhov M, Olenichev A, Orlov S, Turin I, Loginov M, Rautbart S, Baymukanov A, Parshikov V, Demeshonok V, Yakovlev A, Druzhkova T, Guekht A, Gulyaeva N.
PMID: 34559375
Metab Brain Dis. 2021 Dec;36(8):2473-2482. doi: 10.1007/s11011-021-00837-x. Epub 2021 Sep 24.

Dysphagia and progressive swallowing problems due to motoneuron death is one of amyotrophic lateral sclerosis (ALS) symptoms. Malnutrition and body weight loss result in immunological disturbances, fatigability and increase risk of secondary complications in ALS patients, percutaneous endoscopic gastrostomy...

Novel Compound Heterozygous Variants in the .

The application of clinical genetics

Zabnenkova V, Shchagina O, Makienko O, Matyushchenko G, Ryzhkova O.
PMID: 35023948
Appl Clin Genet. 2022 Jan 06;15:1-10. doi: 10.2147/TACG.S342804. eCollection 2022.

BACKGROUND: Meier-Gorlin syndrome (MGS) is a rare genetic syndrome inherited in an autosomal dominant or autosomal recessive manner. The disorder is characterized by bilateral microtia, absence or hypoplasia of the patella, and an intrauterine growth retardation as well as...

2-Imino-2,3-dihydrobenzoxazole-a useful platform for designing rare- and alkaline earth complexes with variable di- and trianionic O,N,N, ligands.

Dalton transactions (Cambridge, England : 2003)

Basalov IV, Kissel AA, Nikolaevskaya EN, Druzhkov NO, Cherkasov AV, Long J, Larionova J, Fukin GK, Trifonov AA.
PMID: 35029255
Dalton Trans. 2022 Jan 14; doi: 10.1039/d1dt04139h. Epub 2022 Jan 14.

The reactions of 2-imino-2,3-dihydrobenzoxazole LH with M[N(SiMe

Showing 1 to 12 of 30 entries