Results 11 to 20 of about 144,082 (199)

Low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with a favorable fetal outcome, intrauterine growth restriction, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes and perinatal progressive decrease of the aneuploid cell line

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2023
Objective: We present low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with a favorable fetal outcome, intrauterine growth restriction (IUGR), cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes and ...
Chih-Ping Chen   +9 more
doaj   +1 more source

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2013
Objective: To present prenatal diagnosis of mosaic trisomy 2. Materials and Methods: A 29-year-old woman underwent amniocentesis at 17 weeks of gestation because of abnormal maternal serum screening, and the cytogenetic result was 47,XY,+2[8]/46,XY[22 ...
Chih-Ping Chen   +8 more
doaj   +1 more source

Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2010
Objective: To present the perinatal findings and molecular cytogenetic analysis of a rare chromosomal abnormality involving structural and numerical abnormalities of chromosome 18.
Chih-Ping Chen   +10 more
doaj   +1 more source

Mosaicism for Robertsonian jumping translocation at amniocentesis: 45,XY,der(15;22)(q10;q10)mat/46,XY,i(15)(q10)/46,XY, genetic counseling, prenatal diagnosis and postnatal follow-up in a pregnancy with a favorable fetal outcome

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2023
Objective: We present genetic counseling, prenatal diagnosis and postnatal follow-up of 45,XY,der(15;22)(q10;q10)mat/46,XY,i(15)(q10)/46,XY at amniocentesis in a pregnancy with a favorable fetal outcome.
Chih-Ping Chen   +7 more
doaj   +1 more source

Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the Literature

open access: yesJCRPE
Swyer syndrome is a rare congenital condition that serves as a risk factor for developing germ cell tumors. The condition belongs to the group of 46, XY disorders of sexual development, is characterized by complete gonadal dysgenesis (CGD) and is mostly ...
Maamoun Adra   +8 more
doaj   +1 more source

Complex clinico-endocrinological characterization of the idiopathic variant of congenital disorder of sex development in a child with male karyotype 46,XY

open access: yesКлинический разбор в общей медицине
Background. Congenital disorders of sex development (DSD) represent a heterogeneous group of dysontogenetic conditions characterized by a discordance between chromosomal, gonadal, and phenotypic sex.
Svyatoslav M. Yurin   +5 more
doaj   +1 more source

A Note on Multiplicative (Generalized) (α, β)-Derivations in Prime Rings

open access: yesAnnales Mathematicae Silesianae, 2019
Let R be a prime ring with center Z(R). A map G : R →R is called a multiplicative (generalized) (α, β)-derivation if G(xy)= G(x)α(y)+β(x)g(y) is fulfilled for all x; y ∈ R, where g : R → R is any map (not necessarily derivation) and α; β : R → R are ...
Rehman Nadeem ur   +2 more
doaj   +1 more source

Hydrostatic pressure activates HIF‐1α via β‐catenin to promote stemness in breast cancer cells

open access: yesFEBS Open Bio, EarlyView.
To mimic the elevated intestinal fluid pressure in breast cancers, we loaded human breast cancer cells (MCF‐7, MDA‐MB‐453, and BT‐474) to 50 mmHg hydrostatic pressure. Hydrostatic pressure exposure upregulated HIF‐1α and induced stemness in MCF‐7 and BT‐474 cells.
Da Zhai   +8 more
wiley   +1 more source

An exposition on complete androgen insensitivity syndrome and a case report

open access: yesАкушерство, гинекология и репродукция
Complete androgen insensitivity syndrome (CAIS) is a rare X-linked sexual development condition typified by 46,XY karyotype, presence of external female genitalia along with intra-abdominal testes in labia majora or inguinal ring region.
S. Morkos   +8 more
doaj   +1 more source

A new flow chip in combination with multiphoton microscopy as a protocol for longitudinal 3D imaging of tissue calcification under shear stress

open access: yesFEBS Open Bio, EarlyView.
Miniaturized flow chip platform enabling continuous perfusion and longitudinal multiphoton 3D imaging of vascular smooth muscle cell constructs under physiological flow. Brightfield imaging guides region selection, while CellTracker Green and mRuby‐labeled fetuin‐A visualize cells and mineral deposition, respectively. Magnesium supplementation markedly
Vytautas Kučikas   +6 more
wiley   +1 more source

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