Cover Image

Analysis CYP21A2 gene mutations technique in patients with congenital adrenal hyperplasia

Saved in:

Bibliographic Details
Date:	2014
Main Authors:	Yu. Chernushyn, L. A. Livshyts
Format:	Article
Language:	English
Published:	2014
Series:	Biotechnologia Acta
Online Access:	http://jnas.nbuv.gov.ua/article/UJRN-0000426865
Tags:	Add Tag No Tags, Be the first to tag this record!
Journal Title:	Library portal of National Academy of Sciences of Ukraine \| LibNAS

Institution

Library portal of National Academy of Sciences of Ukraine | LibNAS

Similar Items

Is congenital adrenal hyperplasia due to 21- hydroxylase deficiency deceptive disease? Management and differentiation of syndrome in adults
by: A. Nowak
Published: (2017)

New techniques for mutation analysis in some exons of PAH and CFTR gene of men using denaturing gradient gel-electrophoresis
by: O. O. Soloviov, et al.
Published: (2008)

Analysis of mutations in GBA gene in Ukrainian patients with Gaucher disease
by: N. V. Olkhovych, et al.
Published: (2017)

Combined polymorphism of CYP2S9 and CYP2S19 in tuberculosis patients and its impact on serum rifampicin level
by: H. O. Poludenko, et al.
Published: (2019)

Results of mutation status gene HER-2/NEU in patients with breast cancer in Ukraine
by: B. T. Klimuk, et al.
Published: (2017)

The use of hormone therapy at atypical endometria hyperplasia in patients with microsatellite instability and ESR gene methylation
by: N. A. Shcherbina, et al.
Published: (2012)

Mutation analysis of the phenylalanine hydroxylase gene of phenylketonuria patients of Kemerovskaya oblast and Saha Republic
by: O. A. Baturina, et al.
Published: (2012)

Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability
by: R. V. Gulkovskyi, et al.
Published: (2015)

Surgical correction of congenital penile deviations
by: A. V. Arkatov
Published: (2016)

CYP4 and CYP6 gene variability in genome of Aphis fabae mordvilkoi Bцrner &amp; Janisch, 1922
by: N. V. Voronova, et al.
Published: (2018)

The features blood lipid profile in patients with adenomatous and glandular endometrial hyperplasia
by: O. A. Kuzmina
Published: (2013)

Clinical and genealogical study of patients with endometrial hyperplasia and cancer in Kyiv region
by: L. H. Buchynska, et al.
Published: (2017)

The observation of congenital retroperitoneal large size neuroblastoma
by: Starchenko, I.I., et al.
Published: (2023)

Gene expression of polyamine metabolism proteins in human prostate cancer and benign prostatic hyperplasia
by: V. V. Bentrad, et al.
Published: (2020)

Testing polymorphic gene variants of CYP 2D6*4 in patients with benign disease and female reproductive system cancer from the families with family cancer syndrome
by: O. V. Paliichuk, et al.
Published: (2017)

Clinical and laboratory characteristics of acute kidney damage in patients with benign prostatic hyperplasia
by: Ja. Kvasnevskij, et al.
Published: (2019)

Mutations in gene ATP7B in ukrainian patients with high risk of Wilson&#039;s disease
by: H. Makukh, et al.
Published: (2020)

Mutation 6174delT in the BRCA2 gene in men with prostate cancer in Ukraine
by: Ye. V. Horodetska, et al.
Published: (2018)

The changes in indicators of congenital immunity in patients with mixed urogenital protozoan viral infection when ozone therapy is applied
by: I. E. Lukjanov, et al.
Published: (2013)

Biometric analysis of transgenic plants of spring rape with cyp11A1 animal origin gene and bacterial bar
by: A. M. Shishlova-Sokolovskaja, et al.
Published: (2017)

Rare case of nodular lymphoid hyperplasia of left lung in the patient with previous pulmonary tuberculosis
by: Kuzyk, P.V., et al.
Published: (2018)

Screening for mutations in BRCA1 and BRCA2 genes and related perspectives for the healthcare system
by: Ya. O. Tabaliuk, et al.
Published: (2020)

Congenital malformations of the fetus in the structure of infant mortality in Odessa region
by: S. R. Halych, et al.
Published: (2015)

Content of metallothionein in the prostate gland tissue of the senior age patients with bleaching hyperplasia and prostate carcinoma
by: O. H. Pykhtieieva, et al.
Published: (2018)

Drug therapy of lower urinary tract symptoms in patients with benign prostatic hyperplasia: what is new?
by: T. I. Ermolenko
Published: (2015)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis I: identification of three new mutations in α-L-iduronidase gene
by: Trofimova, N.S., et al.
Published: (2016)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene
by: N. S. Trofimova, et al.
Published: (2016)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis I: identification of three new mutations in б-L-iduronidase gene
by: N. S. Trofimova, et al.
Published: (2016)

Spectrum of mutations in patients with organic acidurias from Ukraine
by: Barvinska, O.I., et al.
Published: (2018)

Analysis of MLH1, MSH2 and CAS 20q13 mutations in platinum refractory patients with the ovarian cancer
by: V. G. Dubinina, et al.
Published: (2014)

Mutations in the gene of human type IIb sodium-phosphate cotransporter SLC34A2
by: Lituiev, D.S., et al.
Published: (2010)

Mutation 6174delt in BRCA2 gene in family with tumor pathology aggregation (clinical case)
by: O. V. Paliichuk, et al.
Published: (2015)

Mutation analysis of the PAH gene in Ukrainian population, a report from west Ukraine region
by: H. V. Makukh, et al.
Published: (2021)

Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease
by: N. Y. Mytsyk, et al.
Published: (2016)

Biochemical composition of seeds of transgenic spring rapeseed plants carrying the Mammalia cyp11a1 gene
by: A. M. Shishlova-Sokolovskaya, et al.
Published: (2020)

Unique SARS¬CoV¬2 variant exhibiting plenteous missense mutations in structural and nonstructural genes
by: T. M.S. Alnoura, et al.
Published: (2021)

ESR1 gene allelic polymorphism analysis in population of Ukraine
by: H. B. Livshyts, et al.
Published: (2012)

Biomolecular markers in pathogenesis of development of endometrial hyperplasia
by: T. L. Viesich, et al.
Published: (2019)

The combination of chromosomal reorganization and inherited point mutation has led to the development of a rare clinical phenotype in a patient with disorder of sex differentiation and neuromuscular pathology
by: L. V. Popovych, et al.
Published: (2022)

Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis
by: L. A. Livshits, et al.
Published: (2013)