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...

Swimming Suppresses Cognitive Decline of HFD-Induced Obese Mice through Reversing Hippocampal Inflammation, Insulin Resistance, and BDNF Level

Nutrients, 2022-06, Vol.14 (12), p.2432

2022

Volltextzugriff (PDF)

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

PloS one, 2017-05, Vol.12 (5), p.e0177685-e0177685

2017

Volltextzugriff (PDF)

A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral head

PloS one, 2014-06, Vol.9 (6), p.e100505-e100505

2014

Volltextzugriff (PDF)

A Novel Clerodane-Type Diterpenoid from Sheareria nana

Chemistry of natural compounds, 2018, Vol.54 (1), p.81-83

2018

Volltextzugriff (PDF)

Chromatographic fingerprint and the simultaneous determination of five bioactive components of geranium carolinianum L. water extract by high performance liquid chromatography

International journal of molecular sciences, 2011-12, Vol.12 (12), p.8740-8749

2011

Volltextzugriff (PDF)

A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

BMC ophthalmology, 2014-09, Vol.14 (1), p.108-108, Article 108

2014

Volltextzugriff (PDF)

Activation of calcium-sensing receptor increases TRPC3/6 expression in T lymphocyte in sepsis

Molecular immunology, 2015-03, Vol.64 (1), p.18-25

2015

Volltextzugriff (PDF)

Calcium-sensing receptor in the T lymphocyte enhanced the apoptosis and cytokine secretion in sepsis

Molecular immunology, 2015-02, Vol.63 (2), p.337-342

2015

Volltextzugriff (PDF)

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

BMC urology, 2014-08, Vol.14 (1), p.70-70, Article 70

2014

Volltextzugriff (PDF)

Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

Reproductive biology and endocrinology, 2014-08, Vol.12 (1), p.79-79, Article 79

2014

Volltextzugriff (PDF)

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family

BMC medical genetics, 2014-08, Vol.15 (1), p.97-97, Article 97

2014

Volltextzugriff (PDF)

46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature

BMC urology, 2014-12, Vol.14 (1), p.104-104, Article 104

2014

Volltextzugriff (PDF)

A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development

Molecular cytogenetics, 2014-02, Vol.7 (1), p.16-16, Article 16

2014

Volltextzugriff (PDF)

A duplication upstream of SOX9 was not positively correlated with the SRY-negative 46,XX testicular disorder of sex development: A case report and literature review

Molecular medicine reports, 2015-10, Vol.12 (4), p.5659-5664

2015

Volltextzugriff (PDF)

The Timing of Sexual Debut Among Chinese Youth

International perspectives on sexual and reproductive health, 2012-12, Vol.38 (4), p.196-204

2012

Volltextzugriff (PDF)

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report

Molecular medicine reports, 2015-07, Vol.12 (1), p.155-158

2015

Volltextzugriff (PDF)

Target gene panel method versus whole-exome sequencing in detection of idiopathic hypogonadotropic hypogonadism in males

Zhonghua nan ke xue, 2021-10, Vol.27 (10), p.899

2021

Volltextzugriff (PDF)

A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria

Journal of genetics, 2014-08, Vol.93 (2), p.523-525

2014

Volltextzugriff (PDF)

A novel mild variant of osteogenesis imperfecta type I caused by a Gly1088Glu mutation in COL1A1

Molecular medicine reports, 2014-06, Vol.9 (6), p.2187-2190

2014

Volltextzugriff (PDF)

Correlation between microRNA-34b/c single nucleotide polymorphism rs4938723 and male infertility

Zhonghua nan ke xue, 2020-09, Vol.26 (9), p.807

2020

Volltextzugriff (PDF)

Detection of DPY19L2 gene mutation in 2 cases of globozoospermia

Zhonghua nan ke xue, 2020-07, Vol.26 (7), p.620

2020

Volltextzugriff (PDF)

Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens

Zhonghua nan ke xue, 2019-03, Vol.25 (3), p.231

2019

Volltextzugriff (PDF)

Correlation of single nucleotide polymorphisms rs995030 and rs4474514 of the KITLG gene with male infertility

Zhonghua nan ke xue, 2019-06, Vol.25 (6), p.529

2019

Volltextzugriff (PDF)

Self-powered and broadband germanium/PEDOT:PSS heterojunction photodetectors for near-infrared biomedical imaging applications

Science China. Technological sciences, 2021-11, Vol.64 (11), p.2523-2531

2021

Volltextzugriff (PDF)

FSH and FSHR gene polymorphisms and male infertility: An update

Zhonghua nan ke xue, 2015-11, Vol.21 (11), p.1031

2015

Volltextzugriff (PDF)

1 – 25 von 393

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(311)
Mit Volltextzugriff
(325)

Publikationsform

Sprache

Englisch
(336)
Chinesisch
(59)

Erscheinungsjahr

n.n

Thema

Science & Technology
(252)
Life Sciences & Biomedicine
(156)
Humans
(91)
Technology
(75)
Physical Sciences
(72)
Male
(58)
Female
(42)
Chemistry
(39)
Engineering
(35)
Adult
(32)
Materials Science
(32)
Animals
(28)
Materials Science, Multidisciplinary
(28)
Science & Technology - Other Topics
(26)
Chemistry, Multidisciplinary
(19)
Chemistry, Physical
(19)
China
(19)
Infertility, Male - Genetics
(19)
Energy & Fuels
(18)
Mutation
(18)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Swimming Suppresses Cognitive Decline of HFD-Induced Obese Mice through Reversing Hippocampal Inflammation, Insulin Resistance, and BDNF Level

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral head

A Novel Clerodane-Type Diterpenoid from Sheareria nana

Chromatographic fingerprint and the simultaneous determination of five bioactive components of geranium carolinianum L. water extract by high performance liquid chromatography

A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

Activation of calcium-sensing receptor increases TRPC3/6 expression in T lymphocyte in sepsis

Calcium-sensing receptor in the T lymphocyte enhanced the apoptosis and cytokine secretion in sepsis

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family

46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature

A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development

A duplication upstream of SOX9 was not positively correlated with the SRY-negative 46,XX testicular disorder of sex development: A case report and literature review

The Timing of Sexual Debut Among Chinese Youth

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report

Target gene panel method versus whole-exome sequencing in detection of idiopathic hypogonadotropic hypogonadism in males

A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria

A novel mild variant of osteogenesis imperfecta type I caused by a Gly1088Glu mutation in COL1A1

Correlation between microRNA-34b/c single nucleotide polymorphism rs4938723 and male infertility

Detection of DPY19L2 gene mutation in 2 cases of globozoospermia

Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens

Correlation of single nucleotide polymorphisms rs995030 and rs4474514 of the KITLG gene with male infertility

Self-powered and broadband germanium/PEDOT:PSS heterojunction photodetectors for near-infrared biomedical imaging applications

FSH and FSHR gene polymorphisms and male infertility: An update

Suchergebnisse filtern