UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Galectin-1 expression in the serum and placenta of pregnant women with fetal growth restriction and its significance

BMC pregnancy and childbirth, 2021-01, Vol.21 (1), p.14-14, Article 14

2021

Volltextzugriff (PDF)

The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study

Asian journal of andrology, 2020-11, Vol.22 (6), p.642-648

2020

Volltextzugriff (PDF)

Insufficient maintenance DNA methylation is associated with abnormal embryonic development

BMC medicine, 2012-03, Vol.10 (1), p.26-26, Article 26

2012

Volltextzugriff (PDF)

Effects of pre-pregnancy body mass index and gestational weight gain on neonatal birth weight

Journal of Zhejiang University. B. Science, 2017-03, Vol.18 (3), p.263-271

2017

Volltextzugriff (PDF)

Whole-Exome Sequencing Revealed Mutations of MED12 and EFNB1 in Fetal Agenesis of the Corpus Callosum

Frontiers in genetics, 2019-11, Vol.10, p.1201

2019

Volltextzugriff (PDF)

Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene

Journal of Zhejiang University. B. Science, 2019-09, Vol.20 (9), p.753-765

2019

Volltextzugriff (PDF)

Assisted reproductive technology may increase clinical mutation detection in male offspring

Fertility and sterility, 2008-07, Vol.90 (1), p.92-96

2008

Volltextzugriff (PDF)

Clinical Application of Noninvasive Prenatal Testing for Pregnant Women with Assisted Reproductive Pregnancy

International journal of women's health, 2021-01, Vol.13, p.1167-1174

2021

Volltextzugriff (PDF)

Endoplasmic reticulum stress induced by oxidative stress in decidual cells: a possible mechanism of early pregnancy loss

Molecular biology reports, 2012-09, Vol.39 (9), p.9179-9186

2012

Volltextzugriff (PDF)

Poor ovarian response to gonadotropin stimulation is associated with low expression of follicle-stimulating hormone receptor in granulosa cells

Fertility and sterility, 2007-06, Vol.87 (6), p.1350-1356

2007

Volltextzugriff (PDF)

Attenuated oocyte fertilization and embryo development associated with altered growth factor/signal transduction induced by endometriotic peritoneal fluid

Fertility and sterility, 2010-05, Vol.93 (8), p.2538-2544

2010

Volltextzugriff (PDF)

Bone morphogenetic protein-15 in follicle fluid combined with age may differentiate between successful and unsuccessful poor ovarian responders

Reproductive biology and endocrinology, 2012-12, Vol.10 (1), p.116-116, Article 116

2012

Volltextzugriff (PDF)

Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform

Human genomics, 2019-01, Vol.13 (1), p.1-1, Article 1

2019

Volltextzugriff (PDF)

A feasible diagnostic approach for the translocation carrier from the indication of products of conception

Molecular cytogenetics, 2018-01, Vol.11 (1), p.12-12, Article 12

2018

Volltextzugriff (PDF)

G546A polymorphism of growth differentiation factor-9 contributes to the poor outcome of ovarian stimulation in women with diminished ovarian reserve

Fertility and sterility, 2010-11, Vol.94 (6), p.2490-2492

2010

Volltextzugriff (PDF)

Involvement of cyclin B1 in progesterone-mediated cell growth inhibition, G2/M cell cycle arrest, and apoptosis in human endometrial cell

Reproductive biology and endocrinology, 2009-12, Vol.7 (1), p.144-144, Article 144

2009

Volltextzugriff (PDF)

Adriamycin induces H2AX phosphorylation in human spermatozoa

Asian journal of andrology, 2008-09, Vol.10 (5), p.749-757

2008

Volltextzugriff (PDF)

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease

Scientific reports, 2015-12, Vol.5 (1), p.17468-17468, Article 17468

2015

Volltextzugriff (PDF)

Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis

The journal of maternal-fetal & neonatal medicine, 2019-01, Vol.32 (1), p.38-45

2019

Volltextzugriff (PDF)

An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing

Npj genomic medicine, 2024-05, Vol.9 (1), p.32-9, Article 32

2024

Volltextzugriff (PDF)

Detection of fetal subchromosomal aberration with cell-free DNA screening led to diagnosis of parental translocation: Review of 11344 consecutive cases in a university hospital

European journal of medical genetics, 2019-02, Vol.62 (2), p.115-123

2019

Volltextzugriff (PDF)

Altered aquaporin expression in women with polycystic ovary syndrome: hyperandrogenism in follicular fluid inhibits aquaporin-9 in granulosa cells through the phosphatidylinositol 3-kinase pathway

Human reproduction (Oxford), 2010-06, Vol.25 (6), p.1441-1450

2010

Volltextzugriff (PDF)

Reply of the Authors: Need for standardization and confirmation of STS deletions on the Y chromosome

Fertility and sterility, 2008-08, Vol.90 (2), p.464-464

2008

Volltextzugriff (PDF)

Association of Serum and Follicular Fluid Leptin Concentrations with Granulosa Cell Phosphorylated Signal Transducer and Activator of Transcription 3 Expression in Fertile Patients with Polycystic Ovarian Syndrome

The journal of clinical endocrinology and metabolism, 2007-12, Vol.92 (12), p.4771-4776

2007

Volltextzugriff (PDF)

Preimplantation genetic diagnosis for Down syndrome pregnancy

Journal of Zhejiang University. B. Science, 2007-07, Vol.8 (7), p.515-521

2007

Volltextzugriff (PDF)

1 – 25 von 346

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(231)
Mit Volltextzugriff
(314)

Publikationsform

Sprache

Englisch
(271)
Chinesisch
(75)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Galectin-1 expression in the serum and placenta of pregnant women with fetal growth restriction and its significance

The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study

Insufficient maintenance DNA methylation is associated with abnormal embryonic development

Effects of pre-pregnancy body mass index and gestational weight gain on neonatal birth weight

Whole-Exome Sequencing Revealed Mutations of MED12 and EFNB1 in Fetal Agenesis of the Corpus Callosum

Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene

Assisted reproductive technology may increase clinical mutation detection in male offspring

Clinical Application of Noninvasive Prenatal Testing for Pregnant Women with Assisted Reproductive Pregnancy

Endoplasmic reticulum stress induced by oxidative stress in decidual cells: a possible mechanism of early pregnancy loss

Poor ovarian response to gonadotropin stimulation is associated with low expression of follicle-stimulating hormone receptor in granulosa cells

Attenuated oocyte fertilization and embryo development associated with altered growth factor/signal transduction induced by endometriotic peritoneal fluid

Bone morphogenetic protein-15 in follicle fluid combined with age may differentiate between successful and unsuccessful poor ovarian responders

Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform

A feasible diagnostic approach for the translocation carrier from the indication of products of conception

G546A polymorphism of growth differentiation factor-9 contributes to the poor outcome of ovarian stimulation in women with diminished ovarian reserve

Involvement of cyclin B1 in progesterone-mediated cell growth inhibition, G2/M cell cycle arrest, and apoptosis in human endometrial cell

Adriamycin induces H2AX phosphorylation in human spermatozoa

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease

Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis

An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing

Detection of fetal subchromosomal aberration with cell-free DNA screening led to diagnosis of parental translocation: Review of 11344 consecutive cases in a university hospital

Altered aquaporin expression in women with polycystic ovary syndrome: hyperandrogenism in follicular fluid inhibits aquaporin-9 in granulosa cells through the phosphatidylinositol 3-kinase pathway

Reply of the Authors: Need for standardization and confirmation of STS deletions on the Y chromosome

Association of Serum and Follicular Fluid Leptin Concentrations with Granulosa Cell Phosphorylated Signal Transducer and Activator of Transcription 3 Expression in Fertile Patients with Polycystic Ovarian Syndrome

Preimplantation genetic diagnosis for Down syndrome pregnancy

Suchergebnisse filtern