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Journal ArticleDOI

Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.

TLDR
It is suggested that on the distal portion of the nonfluorescent segment of the long arm of the Y, factors are located controlling spermatogenesis.
Abstract
A deletion of the Y chromosome at the distal portion of band q11 was found in 6 men with normal male habitus but with azoospermia. Five of them were found during a survey of 1170 subfertile males while the sixth was karyotyped because of slight bone abnormalities. These findings, together with a review of the literature, suggest that on the distal portion of the nonfluorescent segment of the long arm of the Y, factors are located controlling spermatogenesis.

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Citations
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Journal ArticleDOI

Mutation analysis of HSFY gene by DNA sequencing in Turkish men with idiopathic infertility

TL;DR: It is suggested that the clinical molecular approach to diagnosis of individuals with spermatogenic failure is complicated due to extensive genetic heterogeneity and need more study to reveal causative genes and mutations of idiopathic infertility in men.
Journal ArticleDOI

Genetics of male infertility and related genes within Y chromosome

TL;DR: This review article will focus on the structural abnormality and related gene functions on infertility that focuses on genetic factors impairing spermatogenesis and structural abnormalities such as Y chromosome microdeletions.

Uso de la acupuntura en el tratamiento de la infertilidad. Revisión sistemática de la literatura

TL;DR: It is concluded that acupuncture is an effective tool for management of infertility in women and in male infertility acupuncture could improve aspects of semen.
Journal ArticleDOI

SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants

TL;DR: SATINN (Software for Analysis of Testis Images with Neural Networks), a multi-level framework for automated analysis of multiplexed immunofluorescence images from mouse testis, and numerous cell- and tubule-level statistics that can be derived from wildtype testis are described.
References
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Journal ArticleDOI

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

TL;DR: Data from a chromosome examination of 14,069 consecutive newborn infants is presented, finding 294 babies with a major chromosome abnormality or distinctive marker chromosomes.
Journal ArticleDOI

Possible role for H--Y antigen in the primary determination of sex.

TL;DR: The part that the X chromosome plays in male sexual differentiation has been clarified at the level of an individual gene situated on this chromosome.
Journal ArticleDOI

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

TL;DR: The results of the present study when combined with five other comparable studies, thus comprising a total of 46,150 newborn infants, indicates that the frequency of major chromosome abnormalities is between 1:150 and 1:200 live-born babies.
Journal ArticleDOI

Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual.

TL;DR: The baseline data presented here reinforce the view that polymorphic chromosome characteristics are very useful markers for characterizing the karyotype of an infant born at the Albert Einstein College Hospital, Bronx, New York, and are consistent with the expectations of the Hardy-Weinberg law.
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