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...

Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia

Journal of medical genetics, 2021-10, Vol.58 (10), p.679-686

2021

Volltextzugriff (PDF)

RNA‐binding protein ELAVL2 plays post‐transcriptional roles in the regulation of spermatogonia proliferation and apoptosis

Cell proliferation, 2021-09, Vol.54 (9), p.e13098-n/a

2021

Volltextzugriff (PDF)

Single-cell transcriptome atlas of the human corpus cavernosum

Nature communications, 2022-07, Vol.13 (1), p.4302-4302, Article 4302

2022

Volltextzugriff (PDF)

A bi‐allelic REC114 loss‐of‐function variant causes meiotic arrest and nonobstructive azoospermia

Clinical genetics, 2024-04, Vol.105 (4), p.440-445

2024

Volltextzugriff (PDF)

A homozygous frameshift variant in SYCP2 caused meiotic arrest and non‐obstructive azoospermia

Clinical genetics, 2023-11, Vol.104 (5), p.577-581

2023

Volltextzugriff (PDF)

Bi‐allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest

Clinical genetics, 2022-05, Vol.101 (5-6), p.507-516

2022

Volltextzugriff (PDF)

Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia

Reproductive biology and endocrinology, 2022-01, Vol.20 (1), p.21-21, Article 21

2022

Volltextzugriff (PDF)

miR-202-3p Regulates Sertoli Cell Proliferation, Synthesis Function, and Apoptosis by Targeting LRP6 and Cyclin D1 of Wnt/β-Catenin Signaling

Molecular therapy. Nucleic acids, 2019-03, Vol.14, p.1-19

2019

Volltextzugriff (PDF)

Low-Intensity Pulsed Ultrasound Alleviates Human Testicular Leydig Cell Senescence In Vitro

International journal of molecular sciences, 2022-12, Vol.24 (1), p.418

2022

Volltextzugriff (PDF)

Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia

Journal of human genetics, 2023-06, Vol.68 (6), p.383-392

2023

Volltextzugriff (PDF)

Vasal vessel‐sparing microsurgical single‐armed vasoepididymostomy to epididymal obstructive azoospermia: A retrospective control study

Andrologia, 2021-09, Vol.53 (8), p.e14133-n/a

2021

Volltextzugriff (PDF)

Preliminary experience with 3D digital image microscope system on the treatment of varicocele

Andrologia, 2022-08, Vol.54 (7), p.1592-1597

2022

Volltextzugriff (PDF)

Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population

Frontiers in genetics, 2021-09, Vol.12, p.741355-741355

2021

Volltextzugriff (PDF)

Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia

BMC medical genomics, 2022-06, Vol.15 (1), p.137-137, Article 137

2022

Volltextzugriff (PDF)

Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia

Frontiers in genetics, 2021-12, Vol.12, p.799886-799886

2021

Volltextzugriff (PDF)

Fibroblast growth factor-5 promotes spermatogonial stem cell proliferation via ERK and AKT activation

Stem cell research & therapy, 2019-01, Vol.10 (1), p.40-40, Article 40

2019

Volltextzugriff (PDF)

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization

Frontiers in endocrinology (Lausanne), 2023-01, Vol.13, p.1099270-1099270

2023

Volltextzugriff (PDF)

Derivation and propagation of spermatogonial stem cells from human pluripotent cells

Stem cell research & therapy, 2020-09, Vol.11 (1), p.1-408, Article 408

2020

Volltextzugriff (PDF)

Stepwise mini-incision microdissection testicular sperm extraction in NOA patients with a history of cryptorchidism: a case–control study

Basic and clinical andrology, 2023-08, Vol.33 (1), p.1-21, Article 21

2023

Volltextzugriff (PDF)

Changing trends in penile prosthesis implantation in China and an overview of postoperative outcomes from a single center

Basic and clinical andrology, 2024-08, Vol.34 (1), p.1-8, Article 10

2024

Volltextzugriff (PDF)

A modified single-armed microsurgical vasoepididymostomy for epididymal obstructive azoospermia: intraoperative choice and postoperative consideration

BMC urology, 2020-08, Vol.20 (1), p.121-121, Article 121

2020

Volltextzugriff (PDF)

Primate‐Specific DAZ Regulates Translation of Cell Proliferation‐Related mRNAs and is Essential for Maintenance of Spermatogonia

Advanced science, 2024-08, Vol.11 (29), p.e2400692-n/a

2024

Volltextzugriff (PDF)

Decreased Expression of KIFC1 in Human Testes with Globozoospermic Defects

Genes, 2016-09, Vol.7 (10), p.75-75

2016

Volltextzugriff (PDF)

Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella

American journal of human genetics, 2017-06, Vol.100 (6), p.854-864

2017

Volltextzugriff (PDF)

Deleterious variant in FAM71D cause male infertility with asthenoteratospermia

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.35-35, Article 35

2024

Volltextzugriff (PDF)

1 – 25 von 52

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(45)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia

RNA‐binding protein ELAVL2 plays post‐transcriptional roles in the regulation of spermatogonia proliferation and apoptosis

Single-cell transcriptome atlas of the human corpus cavernosum

A bi‐allelic REC114 loss‐of‐function variant causes meiotic arrest and nonobstructive azoospermia

A homozygous frameshift variant in SYCP2 caused meiotic arrest and non‐obstructive azoospermia

Bi‐allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest

Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia

miR-202-3p Regulates Sertoli Cell Proliferation, Synthesis Function, and Apoptosis by Targeting LRP6 and Cyclin D1 of Wnt/β-Catenin Signaling

Low-Intensity Pulsed Ultrasound Alleviates Human Testicular Leydig Cell Senescence In Vitro

Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia

Vasal vessel‐sparing microsurgical single‐armed vasoepididymostomy to epididymal obstructive azoospermia: A retrospective control study

Preliminary experience with 3D digital image microscope system on the treatment of varicocele

Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population

Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia

Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia

Fibroblast growth factor-5 promotes spermatogonial stem cell proliferation via ERK and AKT activation

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization

Derivation and propagation of spermatogonial stem cells from human pluripotent cells

Stepwise mini-incision microdissection testicular sperm extraction in NOA patients with a history of cryptorchidism: a case–control study

Changing trends in penile prosthesis implantation in China and an overview of postoperative outcomes from a single center

A modified single-armed microsurgical vasoepididymostomy for epididymal obstructive azoospermia: intraoperative choice and postoperative consideration

Primate‐Specific DAZ Regulates Translation of Cell Proliferation‐Related mRNAs and is Essential for Maintenance of Spermatogonia

Decreased Expression of KIFC1 in Human Testes with Globozoospermic Defects

Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella

Deleterious variant in FAM71D cause male infertility with asthenoteratospermia

Suchergebnisse filtern