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...

A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

Clinical genetics, 2024-07, Vol.106 (1), p.27-36

2024

Volltextzugriff (PDF)

Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

EMBO molecular medicine, 2021-12, Vol.13 (12), p.e14887-n/a

2021

Volltextzugriff (PDF)

Mutant ZP1 in Familial Infertility

The New England journal of medicine, 2014-03, Vol.370 (13), p.1220-1226

2014

Volltextzugriff (PDF)

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

Human mutation, 2021-01, Vol.42 (1), p.31-36

2021

Volltextzugriff (PDF)

Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos

PloS one, 2018-11, Vol.13 (11), p.e0207340-e0207340

2018

Volltextzugriff (PDF)

A newly discovered mutation in PICK1 in a human with globozoospermia

Asian journal of andrology, 2010-07, Vol.12 (4), p.556-560

2010

Volltextzugriff (PDF)

Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

BMC pregnancy and childbirth, 2023-03, Vol.23 (1), p.199-199, Article 199

2023

Volltextzugriff (PDF)

The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Andrologia, 2018-09, Vol.50 (7), p.e13056-n/a

2018

Volltextzugriff (PDF)

Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Frontiers in endocrinology (Lausanne), 2022-02, Vol.13, p.794720-794720

2022

Volltextzugriff (PDF)

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1165-n/a

2020

Volltextzugriff (PDF)

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1662-n/a

2021

Volltextzugriff (PDF)

Abnormalities in centrosome number in human embryos and embryonic stem cells

Molecular reproduction and development, 2016-05, Vol.83 (5), p.392-404

2016

Volltextzugriff (PDF)

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

HGG advances, 2024-01, Vol.5 (1), p.100256-100256, Article 100256

2024

Volltextzugriff (PDF)

Endometrial CD138 count appears to be a negative prognostic indicator for patients who have experienced previous embryo transfer failure

Fertility and sterility, 2019-12, Vol.112 (6), p.1103-1111

2019

Volltextzugriff (PDF)

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00709-n/a

2019

Volltextzugriff (PDF)

Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Genes chromosomes & cancer, 2008-08, Vol.47 (8), p.665-679

2008

Volltextzugriff (PDF)

Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Human reproduction (Oxford), 2023-07, Vol.38 (7), p.1390-1398

2023

Volltextzugriff (PDF)

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

BMC medical genetics, 2018-01, Vol.19 (1), p.15-15, Article 15

2018

Volltextzugriff (PDF)

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Human reproduction (Oxford), 2024-04, Vol.39 (4), p.849-855

2024

Volltextzugriff (PDF)

Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Molecular biology reports, 2011-06, Vol.38 (5), p.3061-3065

2011

Volltextzugriff (PDF)

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Journal of medical genetics, 2023-02, Vol.60 (2), p.144

2023

Volltextzugriff (PDF)

Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency

Molecular genetics & genomic medicine, 2018-03, Vol.6 (2), p.261-267

2018

Volltextzugriff (PDF)

CD19 and intraglandular CD163-positivity as prognostic indicators of pregnancy outcome in CD138-negative women with a previous fresh-embryo-transfer failure

Journal of reproductive immunology, 2021-09, Vol.147, p.103362-103362, Article 103362

2021

Volltextzugriff (PDF)

Transcriptional Activation of Human CDCA8 Gene Regulated by Transcription Factor NF-Y in Embryonic Stem Cells and Cancer Cells

The Journal of biological chemistry, 2015-09, Vol.290 (37), p.22423-22434

2015

Volltextzugriff (PDF)

Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome

Reproductive biomedicine online, 2019-03, Vol.38 (3), p.397-406

2019

Volltextzugriff (PDF)

1 – 25 von 160

Suche als RSS-Feed

Aktive Filter

KollektionMEDLINE

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(75)
Mit Volltextzugriff
(98)

Publikationsform

Artikel
(160)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(131)
Female
(80)
Male
(79)
Science & Technology
(78)
Life Sciences & Biomedicine
(77)
Animals
(52)
Mice
(49)
Adult
(48)
Pregnancy
(33)
Base Sequence
(32)
Molecular Sequence Data
(30)
Amino Acid Sequence
(26)
Cells, Cultured
(22)
Cloning, Molecular
(20)
Biochemistry & Molecular Biology
(19)
Testis - Metabolism
(19)
Reproductive Biology
(18)
Reverse Transcriptase Polymerase Chain Reaction
(17)
Genetics & Heredity
(16)
Pedigree
(16)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

Mutant ZP1 in Familial Infertility

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos

A newly discovered mutation in PICK1 in a human with globozoospermia

Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

Abnormalities in centrosome number in human embryos and embryonic stem cells

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

Endometrial CD138 count appears to be a negative prognostic indicator for patients who have experienced previous embryo transfer failure

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency

CD19 and intraglandular CD163-positivity as prognostic indicators of pregnancy outcome in CD138-negative women with a previous fresh-embryo-transfer failure

Transcriptional Activation of Human CDCA8 Gene Regulated by Transcription Factor NF-Y in Embryonic Stem Cells and Cancer Cells

Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome

Aktive Filter

Suchergebnisse filtern