Galnt3 deficiency disrupts acrosome formation and leads to oligoasthenoteratozoospermia (Q87423212)

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10 March 2020

title

Galnt3 deficiency disrupts acrosome formation and leads to oligoasthenoteratozoospermia (English)

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5

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author name string

Toshihiro Miyazaki

1

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10 March 2020

Masako Mori

2

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10 March 2020

Carolina A Yoshida

3

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Chizuru Ito

4

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10 March 2020

Takeshi Moriishi

6

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10 March 2020

Yosuke Kawai

7

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10 March 2020

Hisato Komori

8

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10 March 2020

Tetsuya Kawane

9

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10 March 2020

Shin-ichi Izumi

10

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Kiyotaka Toshimori

11

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Toshihisa Komori

12

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publication date

28 September 2012

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Histochemistry and Cell Biology

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published in

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volume

139

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issue

2

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page(s)

339-354

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A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis

10 March 2020

cites work

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12 December 2020

Hyperostosis-hyperphosphatemia syndrome: a congenital disorder of O-glycosylation associated with augmented processing of fibroblast growth factor 23.

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12 December 2020

Loss of zona pellucida binding proteins in the acrosomal matrix disrupts acrosome biogenesis and sperm morphogenesis

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12 December 2020

A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis

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Globozoospermia in mice lacking the casein kinase II alpha' catalytic subunit

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An improved culture medium supports development of random-bred 1-cell mouse embryos in vitro

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Significance of the equatorial segment of the acrosome of the spermatozoon in eutherian mammals

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A lectin recognizes differential arrangements of O-glycans on mucin repeats

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12 December 2020

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

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12 December 2020

Dietary phosphate restriction normalizes biochemical and skeletal abnormalities in a murine model of tumoral calcinosis

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Dynamics of the mammalian sperm head: modifications and maturation events from spermatogenesis to egg activation.

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Lack of acrosome formation in mice lacking a Golgi protein, GOPC.

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A guide for carbohydrate specificities of lectins

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12 December 2020

Polypeptide GalNAc-transferase T3 and familial tumoral calcinosis. Secretion of fibroblast growth factor 23 requires O-glycosylation

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12 December 2020

cDNA cloning and expression of a novel human UDP-N-acetyl-alpha-D-galactosamine. Polypeptide N-acetylgalactosaminyltransferase, GalNAc-t3

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12 December 2020

DPY19L2 deletion as a major cause of globozoospermia

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12 December 2020

PICK1 deficiency causes male infertility in mice by disrupting acrosome formation

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12 December 2020

Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations

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12 December 2020

Globozoospermia revisited

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12 December 2020

Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family.

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12 December 2020

Expression of uridine diphosphate N-acetyl-alpha-D-galactosamine: polypeptide N-acetylgalactosaminyl transferase 3 in adenocarcinoma of the pancreas

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12 December 2020

Lack of acrosome formation in Hrb-deficient mice

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12 December 2020

Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia

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12 December 2020

Carbohydrate binding specificity of the Tn-antigen binding lectin from Vicia villosa seeds (VVLB4)

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12 December 2020

Changes in the profile of simple mucin-type O-glycans and polypeptide GalNAc-transferases in human testis and testicular neoplasms are associated with germ cell maturation and tumour differentiation.

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12 December 2020

Spermatogenesis of mice lacking CK2alpha': failure of germ cell survival and characteristic modifications of the spermatid nucleus.

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12 December 2020

A model of the acrosome reaction progression via the acrosomal membrane-anchored protein equatorin

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12 December 2020

Equatorin: identification and characterization of the epitope of the MN9 antibody in the mouse

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12 December 2020

Failure to assemble the peri-nuclear structures in GOPC deficient spermatids as found in round-headed spermatozoa.

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12 December 2020

An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.

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12 December 2020

A newly discovered mutation in PICK1 in a human with globozoospermia

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12 December 2020

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation

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12 December 2020

A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification

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12 December 2020

Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men.

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12 December 2020

Amino acid sequences of porcine Sp38 and proacrosin required for binding to the zona pellucida

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12 December 2020

Ablation of the Galnt3 gene leads to low-circulating intact fibroblast growth factor 23 (Fgf23) concentrations and hyperphosphatemia despite increased Fgf23 expression

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12 December 2020

An MN9 antigenic molecule, equatorin, is required for successful sperm-oocyte fusion in mice

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12 December 2020

Characterization of the antigen recognized by a monoclonal antibody MN9: unique transport pathway to the equatorial segment of sperm head during spermiogenesis

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12 December 2020

Low expression of polypeptide GalNAc N-acetylgalactosaminyl transferase-3 in lung adenocarcinoma: impact on poor prognosis and early recurrence

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12 December 2020

Physiological changes in the postnuclear cap region of mammalian spermatozoa: A necessary preliminary to the membrane fusion between sperm and egg cells

1 reference

12 December 2020

Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders

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12 December 2020

A mouse model of familial oligoasthenoteratozoospermia

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12 December 2020

Inhibition of mouse fertilization in vivo by intra-oviductal injection of an anti-equatorin monoclonal antibody.

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12 December 2020

Purification and characterization of a 38-kDa protein, sp38, with zona pellucida-binding property from porcine epididymal sperm

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12 December 2020

10.1007/S00418-012-1031-3

Identifiers

DOI

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10 March 2020

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