Lack of LGR8 gene mutation in Finnish patients with a family history of cryptorchidism (Q34281105)

1 August 2017

title

Lack of LGR8 gene mutation in Finnish patients with a family history of cryptorchidism (English)

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1 August 2017

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6

Jorma Toppari

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1 August 2017

Jaesook Roh

1

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ORCID Public Data File 2021

author name string

Helena Virtanen

2

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1 August 2017

Jin Kumagai

3

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1 August 2017

Satoko Sudo

4

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1 August 2017

Marko Kaleva

5

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1 August 2017

Aaron J W Hsueh

7

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1 August 2017

publication date

1 October 2003

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Reproductive BioMedicine Online

1 August 2017

published in

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1 August 2017

volume

7

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1 August 2017

issue

4

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1 August 2017

page(s)

400-406

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Müllerian-inhibiting substance function during mammalian sexual development

1 August 2017

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High-efficiency transformation of mammalian cells by plasmid DNA

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Genetics of Undescended Testis

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Vasoactive intestinal peptide: a novel stimulator of steroidogenesis by cultured rat granulosa cells

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Mutations of the GREAT gene cause cryptorchidism

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7 January 2021

The Three Subfamilies of Leucine-Rich Repeat-Containing G Protein-Coupled Receptors (LGR): Identification of LGR6 and LGR7 and the Signaling Mechanism for LGR7

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7 January 2021

The hormonal control of testicular descent

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7 January 2021

Anatomical and functional aspects of testicular descent and cryptorchidism

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7 January 2021

Analysis of homeobox gene HOXA10 mutations in cryptorchidism

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7 January 2021

A common polymorphism in the human relaxin-like factor (RLF) gene: no relationship with cryptorchidism

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7 January 2021

Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

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7 January 2021

Transmembrane regions V and VI of the human luteinizing hormone receptor are required for constitutive activation by a mutation in the third intracellular loop

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7 January 2021

INSL3/Leydig insulin-like peptide activates the LGR8 receptor important in testis descent

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7 January 2021

Paternity after cryptorchidism: lack of correlation with age at orchidopexy

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7 January 2021

Genetic analysis of the INSL3 gene in patients with maldescent of the testis

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7 January 2021

Different insulin-like 3 (INSL3) gene mutations not associated with human cryptorchidism

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7 January 2021

Genetic analysis of the Müllerian-inhibiting substance signal transduction pathway in mammalian sexual differentiation

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7 January 2021

Cryptorchidism in mice mutant for Insl3

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7 January 2021

A transgenic insertion causing cryptorchidism in mice

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Cryptorchidism and homeotic transformations of spinal nerves and vertebrae in Hoxa-10 mutant mice

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7 January 2021

Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice

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7 January 2021

Ala/Thr60 variant of the Leydig insulin-like hormone is not associated with cryptorchidism in the Japanese population

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7 January 2021

Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism

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7 January 2021

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7 January 2021

Trends in the incidence of cryptorchidism and hypospadias, and methodological limitations of registry-based data

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7 January 2021

Risk factors for cryptorchidism and hypospadias

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7 January 2021

Targeted disruption of the Insl3 gene causes bilateral cryptorchidism

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7 January 2021

10.1016/S1472-6483(10)61883-4

Identifiers

DOI

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1 August 2017

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