(Q80286413)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16983454%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

title

Is a genetic defect in Fkbp6 a common cause of azoospermia in humans? (English)

1 reference

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30 December 2019

author name string

Toshinobu Miyamato

1

1 reference

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30 December 2019

Hisashi Sato

2

1 reference

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30 December 2019

Leah Yogev

3

1 reference

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30 December 2019

Sandra Kleiman

4

1 reference

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30 December 2019

Mikio Namiki

5

1 reference

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30 December 2019

Eitetsu Koh

6

1 reference

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30 December 2019

Naoko Sakugawa

7

1 reference

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30 December 2019

Hiroaki Hayashi

8

1 reference

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30 December 2019

Mutsuo Ishikawa

9

1 reference

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30 December 2019

Dolores J Lamb

10

1 reference

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30 December 2019

Kazuo Sengoku

11

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30 December 2019

publication date

14 September 2006

1 reference

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Cellular & Molecular Biology Letters

30 December 2019

published in

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30 December 2019

volume

11

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30 December 2019

page(s)

557-569

1 reference

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30 December 2019

issue

4

1 reference

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https://scigraph.springernature.com/pub.10.2478/s11658-006-0043-1

30 December 2019

exact match

0 references

cites work

Mechanistic links between nonsense-mediated mRNA decay and pre-mRNA splicing in mammalian cells

1 reference

12 December 2020

Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia

1 reference

12 December 2020

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

1 reference

12 December 2020

A novel human gene FKBP6 is deleted in Williams syndrome

1 reference

12 December 2020

Meiotic chromosomes: integrating structure and function

1 reference

12 December 2020

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

12 December 2020

Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm.

1 reference

12 December 2020

A locus responsible for arrest of spermatogenesis is located on rat Chromosome 12

1 reference

12 December 2020

Testicular disruption in the As (aspermia) mutant rat, with special reference to the aggregate of ribosomes.

1 reference

12 December 2020

Female germ cell aneuploidy and embryo death in mice lacking the meiosis-specific protein SCP3

1 reference

12 December 2020

An aspermia rat mutant (as/as) with spermatogenic failure at meiosis

1 reference

12 December 2020

Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis

1 reference

12 December 2020

The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility

1 reference

12 December 2020

Chromosomal variants among 1790 infertile men

1 reference

12 December 2020

Azoospermia in patients heterozygous for a mutation in SYCP3

1 reference

12 December 2020

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

1 reference

12 December 2020

10.2478/S11658-006-0043-1

Identifiers

DOI

1 reference

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Dimensions Publication ID

30 December 2019

0 references

1 reference

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30 December 2019

1 reference