Results 121 to 130 of about 18,943 (253)

Variants in ZZS Complex‐Associated Genes TEX11 and M1AP Are Responsible for Male Infertility and Nonobstructive Azoospermia

open access: yesAndrology, EarlyView.
ABSTRACT Background Nonobstructive azoospermia (NOA) is the most severe form of male infertility, with genetic factors contributing to approximately 30% of cases. However, only a small fraction of all NOA cases can be explained by the current genetic findings.
Ao Ma   +12 more
wiley   +1 more source

No Detectable Fertility Benefit from a Single Additional Mating in Wild Stalk-Eyed Flies

open access: yes, 2010
Background: Multiple mating by female insects is widespread, and the explanation(s) for repeated mating by females has been the subject of much discussion.
Fowler, K   +8 more
core   +1 more source

Can Hormonal Therapy Improve the Outcomes of mTESE in Patients With Non‐Obstructive Azoospermia?

open access: yesAndrology, EarlyView.
ABSTRACT Background Non‐obstructive azoospermia (NOA) represents the most severe form of male infertility. Hypogonadism is common in NOA patients, and normal testosterone (T) levels are considered essential for spermatogenesis. Fertility‐preserving hormonal therapy (FpHT) has been proposed to optimize hormonal milieu and improve sperm retrieval rates ...
Mattia Anfosso   +5 more
wiley   +1 more source

Meiotic behavior and pollen viability in Jatropha curcas L.

open access: yes, 2015
The Jatropha curcas, known as physic nut, belonging to the Euphorbiaceae family, figure today as one of the greatest potential of oilseeds for biodiesel production in Brazil. The present study aimed to evaluate meiosis and pollen viability in J.
Nathália Virgínia da Silva Ribeiro   +4 more
core   +1 more source

Dystrophia Smolandiensis is characterized by a novel NQO1 variant and a distinct phenotype from COL17A1‐associated epithelial recurrent erosion dystrophy

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To determine the molecular cause of the two epithelial recurrent erosion dystrophies, Dystrophia Smolandiensis and Dystrophia Helsinglandica, and to identify phenotypic differences between the two conditions. Methods DNA samples and clinical data from structured interview records were obtained from the Swedish families in which ...
Karl De Geer   +5 more
wiley   +1 more source

The Embryonic Development of the Cotylean Polyclad Phrikoceros jannetae

open access: yesActa Zoologica, EarlyView.
ABSTRACT Polyclads exhibit distinct developmental modes ranging from direct to indirect development, with several transitional stages also recognised. The existence of an indirect developmental mode in polyclads with a planktonic life history stage in the form of a free‐swimming larva is unique among all free‐living flatworms and makes polyclads a ...
Mehrez Gammoudi   +6 more
wiley   +1 more source

Anatomical and Histological Structures of the Male Reproductive System of Chalcophora mariana (Linnaeus, 1758) (Coleoptera: Buprestidae): Light and Scanning Electron Microscopy Study

open access: yesActa Zoologica, EarlyView.
ABSTRACT This study presents the first detailed morphological analysis of the male reproductive system of Chalcophora mariana (Linnaeus, 1758) using stereo microscopy, light microscopy, and scanning electron microscopy. The male reproductive system of C.
Hicret Arslan, Selami Candan
wiley   +1 more source

Chromosomes and their meiotic behavior in twelve species of the subfamily Harpactorinae (Hemiptera: Heteroptera: Reduviidae) from north India

open access: yes, 2013
Kaur, Rajdeep, Kaur, Harbhajan (2013): Chromosomes and their meiotic behavior in twelve species of the subfamily Harpactorinae (Hemiptera: Heteroptera: Reduviidae) from north India. Zootaxa 3694 (4): 358-366, DOI: 10.11646/zootaxa.3694.4.
Kaur, Harbhajan, Kaur, Rajdeep
core   +1 more source

From a novel pathogenic SAMD9L variant to cohort‐wide insights: Whole‐genome sequencing highlights somatic genetic rescue and phenotypic heterogeneity

open access: yesBritish Journal of Haematology, EarlyView.
Summary Germline gain‐of‐function variants in sterile alpha motif domain–containing 9‐like (SAMD9L), located on chromosome 7q, cause a multisystem disorder characterized by bone marrow failure, immunodeficiency and variable neurological involvement. Disease evolution is frequently shaped by somatic genetic rescue (SGR), most commonly through monosomy 7,
Hadjer Dellal   +10 more
wiley   +1 more source

Live Cell-Imaging of Meiotic Chromosomes in Arabidopsis Meiotic Mutant solo dancers Using Multi-photon Microscope [PDF]

open access: yes
We have been analyzing Arabidopsis meiotic mutant solo dancers (sds) , which show asynapsis between homologous chromosomes, and the resulting sterile phenotype.
コガ, ヒロユキ   +7 more
core   +1 more source

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