Results 191 to 200 of about 14,082 (237)

Derivative (1;18)(q10;q10) in essential thrombocythemia

Cancer Genetics and Cytogenetics, 2010
This study reports the association of the chromosomal abnormality derivative (1;18)(q10;q10) with essential thrombocythemia (ET) occurring in a 75-year-old woman. Allele-specific polymerase chain reaction also revealed a V617F mutation in the Janus Kinase 2 gene (JAK2) in the platelet compartment in this patient.
Taichi, Azuma, Jun, Yamanouchi, Katsuji, Inoue, Masashi, Kohno, Hiroshi, Narumi, Hiroshi, Fujiwara, Yoshihiro, Yakushijin, Takaaki, Hato, Masaki, Yasukawa   +8 more
openaire   +2 more sources

Coenzyme Q10 in Pregnancy

Fetal Diagnosis and Therapy, 2009
Our objectives were to assess the plasma coenzyme Q10 (CoQ10) levels in normal pregnancy, in pregnancy with a spontaneous contractile event, in spontaneous abortion and in threatened abortion. Six hundred and fifteen CoQ10 levels were analyzed in 483 pregnant women: 350 patients were employed to design a normal curve; 66 patients with spontaneous ...
Noia, Giuseppe, Littarru, Gp, De Santis, Marco, Oradei, A, Mastromarino, C, Trivellini, C, Caruso, Alessandro   +6 more
openaire   +3 more sources

Pharmacokinetics of coenzyme Q10

Bulletin of Experimental Biology and Medicine, 2008
The pharmacokinetics of coenzyme Q10 powder and solution of solubilized form was studied after their oral administration to rats (10 mg/kg). Plasma concentrations of coenzyme Q10 were measured by HPLC with electrochemical detection over 48 hours. Solubilized coenzyme Q10 exhibited high absorption creating higher plasma concentrations of the drug, as a ...
E I, Kalenikova, E A, Gorodetskaya, O S, Medvedev   +2 more
openaire   +2 more sources

Q10

2011
???????????????????????? ?????????????????????? ?????????????????????? ???????????????????? Q10 (????Q10) ???? ?????????????????? ?????????????????????????????? ?????????? ???????????????????????? ???? ?????????????????????? ?????????? ???????????????? ???????????? ???? ???????? ???????????????????? ???? ?????????????????????? ??????????????????????????
openaire   +3 more sources

Waldenström macroglobulinemia with a novel der(8;17)(q10;q10)

Cancer Genetics and Cytogenetics, 2003
We report the occurrence of an unbalanced whole-arm translocation of der(8;17)(q10;q10) in an 80-year-old female patient with Waldenström macroglobulinemia. To our knowledge, der(8;17)(q10;q10) has not been described in Waldenström macroglobulinemia.
openaire   +2 more sources

Coenzyme Q10 in atherosclerosis

European Journal of Pharmacology
Atherosclerotic disease is a chronic disease that predominantly affects the elderly and is the most common cause of cardiovascular death worldwide. Atherosclerosis is closely related to processes such as abnormal lipid transport and metabolism, impaired endothelial function, inflammation, and oxidative stress. Coenzyme Q10 (CoQ10) is a key component of
Minjun Liao, Xueke He, Yangyang Zhou, Weiqiang Peng, Xiao-Mei Zhao, Miao Jiang   +5 more
openaire   +2 more sources

Coenzyme Q10 and male infertility

Journal of Endocrinological Investigation, 2009
We had previously demonstrated that Coenzyme Q10 [(CoQ10) also commonly called ubiquinone] is present in well-measurable levels in human seminal fluid, where it probably exerts important metabolic and antioxidant functions; seminal CoQ10 concentrations show a direct correlation with seminal parameters (count and motility).
Balercia, Giancarlo, Mancini, Antonio, Paggi, F, Tiano, Luca, Pontecorvi, Alfredo, Boscaro, Marco, Lenzi, Andrea, Littarru, Gian Paolo   +7 more
openaire   +4 more sources

Derivative (1;18)(q10;q10)

Cancer Genetics and Cytogenetics, 2001
T.S.K. Wan, S.K. Ma, W.Y. Au, L.C. Chan
openaire   +1 more source

44,X,der(21;22)(q10;q10)[43]/45,XX,der(21;22)(q10;q10)[27] a Case Study of Mosaicism with Menstrual Disorders

Clinical Laboratory
Turner syndrome (TS), also known as congenital ovarian hypoplasia, is one of the most common sex chromosome diseases in women. It is caused by the complete or partial deletion or structural change of one X chromosome in all or part of somatic cells. A rare case of karyotype Turner syndrome is reported.A 16-year-old female presented with oligomenorrhea ...
Cong, Liu, Yan, Lin, Mihua, Liu
openaire   +2 more sources

?????????????????????? ???????????????????????? ???????????????????? ???????????????? 13 ?? 14 ?? ???????????????????????????? ?????????????????? ?????????????????????????????? ???????????????????????? der(13;14)(q10;q10)

2017
???????????????????????? ???????????????????? ???????????????????????? ???????????????????????? ???????????????????????? ???????????????????? ???????????????? 13 ?? 14 ?? ???????????????????????????? ???????? ???????????????????????????? ?????????????????? ?????????????????????????????? ???????????????????????? der(13;14) ?????????????? ????????????????
openaire   +1 more source