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...

Importance of SLC26 Transmembrane Anion Exchangers in Sperm Post-testicular Maturation and Fertilization Potential

Frontiers in cell and developmental biology, 2019-10, Vol.7, p.230-230

Touré, Aminata

2019

Volltextzugriff (PDF)

Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives

International journal of molecular sciences, 2022-04, Vol.23 (7), p.3926

2022

Volltextzugriff (PDF)

Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): Physiological and pathophysiological relevance

The international journal of biochemistry & cell biology, 2014-07, Vol.52, p.58-67

2014

Volltextzugriff (PDF)

The genetic architecture of morphological abnormalities of the sperm tail

Human genetics, 2021-01, Vol.140 (1), p.21-42

2021

Volltextzugriff (PDF)

Genetic causes of male infertility: snapshot on morphological abnormalities of the sperm flagellum

Basic and clinical andrology, 2019-03, Vol.29 (1), p.2-2, Article 2

2019

Volltextzugriff (PDF)

Male Infertility: Genetics, Mechanism, and Therapies

BioMed research international, 2016, Vol.2016, p.1-1

2016

Volltextzugriff (PDF)

Male Infertility: Genetics, Mechanism, and Therapies

BioMed research international, 2016, Vol.2016, p.7372362

2016

Volltextzugriff (PDF)

Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility

Science (American Association for the Advancement of Science), 2021-01, Vol.371 (6525)

2021

Volltextzugriff (PDF)

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

American journal of human genetics, 2020-08, Vol.107 (2), p.330-341

2020

Volltextzugriff (PDF)

The Testis Anion Transporter 1 (Slc26a8) is required for sperm terminal differentiation and male fertility in the mouse

Human molecular genetics, 2007-08, Vol.16 (15), p.1783-1793

2007

Volltextzugriff (PDF)

Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia

American journal of human genetics, 2019-07, Vol.105 (1), p.198-212

2019

Volltextzugriff (PDF)

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

American journal of human genetics, 2014-01, Vol.94 (1), p.95-104

2014

Volltextzugriff (PDF)

Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse

Developmental biology, 2014-02, Vol.386 (2), p.419-427

2014

Volltextzugriff (PDF)

Spermatozoa and Plasmodium zoites: the same way to invade oocyte and host cells?

Microbes and infection, 2012-08, Vol.14 (10), p.874-879

2012

Volltextzugriff (PDF)

Correction to: Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm

Genome Biology, 2019-08, Vol.20 (1), p.160-160, Article 160

2019

Volltextzugriff (PDF)

CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report

Human reproduction (Oxford), 2019-10, Vol.34 (10), p.2071-2079

2019

Volltextzugriff (PDF)

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility

American journal of human genetics, 2018-09, Vol.103 (3), p.400-412

2018

Volltextzugriff (PDF)

Gender equality and the right to health

The Lancet (British edition), 2008-12, Vol.372 (9655), p.2008-2009

2008

Volltextzugriff (PDF)

Malformations de l’appareil flagellaire du spermatozoïde impliquées dans l’infertilité chez l’homme

M.S. Médecine sciences, 2012-05, Vol.28 (5), p.503-511

2012

Volltextzugriff (PDF)

Morphological defects of sperm flagellum implicated in human male infertility

M.S. Médecine sciences, 2012-05, Vol.28 (5), p.503

2012

Volltextzugriff (PDF)

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

American journal of human genetics, 2018-04, Vol.102 (4), p.636-648

2018

Volltextzugriff (PDF)

Deletions on mouse Yq lead to upregulation of multiple X- and Y-linked transcripts in spermatids

Human molecular genetics, 2005-09, Vol.14 (18), p.2705-2715

2005

Volltextzugriff (PDF)

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility

American journal of human genetics, 2016-08, Vol.99 (2), p.489-500

2016

Volltextzugriff (PDF)

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Human genetics, 2021-09, Vol.140 (9), p.1367-1377

2021

Volltextzugriff (PDF)

1 – 25 von 201

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(139)
Mit Volltextzugriff
(165)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Importance of SLC26 Transmembrane Anion Exchangers in Sperm Post-testicular Maturation and Fertilization Potential

Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives

Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): Physiological and pathophysiological relevance

The genetic architecture of morphological abnormalities of the sperm tail

Genetic causes of male infertility: snapshot on morphological abnormalities of the sperm flagellum

Male Infertility: Genetics, Mechanism, and Therapies

Male Infertility: Genetics, Mechanism, and Therapies

Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

The Testis Anion Transporter 1 (Slc26a8) is required for sperm terminal differentiation and male fertility in the mouse

Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia

Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse

Spermatozoa and Plasmodium zoites: the same way to invade oocyte and host cells?

Correction to: Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm

CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility

Gender equality and the right to health

Malformations de l’appareil flagellaire du spermatozoïde impliquées dans l’infertilité chez l’homme

Morphological defects of sperm flagellum implicated in human male infertility

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

Deletions on mouse Yq lead to upregulation of multiple X- and Y-linked transcripts in spermatids

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Suchergebnisse filtern