skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Azoospermia remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Genetic mutations contributing to non-obstructive azoospermia
Genetic mutations contributing to non-obstructive azoospermia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genetic mutations contributing to non-obstructive azoospermia

Peña, Vanessa N. ; Kohn, Taylor P. ; Herati, Amin S.

Best Practice & Research Clinical Endocrinology & Metabolism, 2020-12, Vol.34 (6), p.101479, Article 101479 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

Texto completo disponível

Citações Citado por
2
In silico analysis of microRNA genes in azoospermia factor Y-chromosome microdeletions
In silico analysis of microRNA genes in azoospermia factor Y-chromosome microdeletions
Material Type:
Artigo 		Adicionar ao Meu Espaço

In silico analysis of microRNA genes in azoospermia factor Y-chromosome microdeletions

Ergun, Sercan ; Gunes, Sezgin ; Hekim, Neslihan ; Esteves, Sandro C.

International urology and nephrology, 2022-04, Vol.54 (4), p.773-780 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

Texto completo disponível

Citações Citado por
3
A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts
A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts
Material Type:
Artigo 		Adicionar ao Meu Espaço

A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts

Milunsky, Aubrey ; Milunsky, Jeff M. ; Dong, Weilai ; Hovhannisyan, Hayk ; Oates, Robert D.

Journal of assisted reproduction and genetics, 2020-02, Vol.37 (2), p.471-475 [Periódico revisado por pares]

New York: Springer US

Texto completo disponível

Citações Citado por
4
Y-chromosome genes associated with sertoli cell-only syndrome identified by array comparative genome hybridization
Y-chromosome genes associated with sertoli cell-only syndrome identified by array comparative genome hybridization
Material Type:
Artigo 		Adicionar ao Meu Espaço

Y-chromosome genes associated with sertoli cell-only syndrome identified by array comparative genome hybridization

Lan, Kuo-Chung ; Wang, Hung-Jen ; Wang, Tzu-Jou ; Lin, Hsin-Jung ; Chang, Yung-Chiao ; Kang, Hong-Yo

Biomedical Journal, 2023-04, Vol.46 (2), p.100524-100524, Article 100524 [Periódico revisado por pares]

United States: Elsevier B.V

Texto completo disponível

Citações Citado por
5
A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population
A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population
Material Type:
Artigo 		Adicionar ao Meu Espaço

A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population

Wu, B. ; Lu, N.X. ; Xia, Y.K. ; Gu, A.H. ; Lu, C.C. ; Wang, W. ; Song, L. ; Wang, S.L. ; Shen, H.B. ; Wang, X.R.

Human reproduction (Oxford), 2007-04, Vol.22 (4), p.1107-1113 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
6
Copy‐number analysis of Y‐linked loci in young men with non‐obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome Y
Copy‐number analysis of Y‐linked loci in young men with non‐obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome Y
Material Type:
Artigo 		Adicionar ao Meu Espaço

Copy‐number analysis of Y‐linked loci in young men with non‐obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome Y

Suzuki, Erina ; Kobori, Yoshitomo ; Katsumi, Momori ; Ushijima, Kikumi ; Uchiyama, Toru ; Okada, Hiroshi ; Miyado, Mami ; Fukami, Maki

Reproductive medicine and biology, 2020-04, Vol.19 (2), p.178-181 [Periódico revisado por pares]

Japan: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
7
Bridging the Gap between AZF Microdeletions and Karyotype: Twelve Years' Experience of an Infertility Center
Bridging the Gap between AZF Microdeletions and Karyotype: Twelve Years' Experience of an Infertility Center
Material Type:
Artigo 		Adicionar ao Meu Espaço

Bridging the Gap between AZF Microdeletions and Karyotype: Twelve Years' Experience of an Infertility Center

Kalantari, Hamid ; Sabbaghian, Marjan ; Vogiatzi, Paraskevi ; Rambhatla, Amarnath ; Agarwal, Ashok ; Colpi, Giovanni M ; Sadighi Gilani, Mohammad Ali

The world journal of men's health, 2023-07, Vol.41 (3), p.659-670 [Periódico revisado por pares]

Korea (South): Korean Society for Sexual Medicine and Andrology

Texto completo disponível

Citações Citado por
8
Deletion of Ck2β gene causes germ cell development arrest and azoospermia in male mice
Deletion of Ck2β gene causes germ cell development arrest and azoospermia in male mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Deletion of Ck2β gene causes germ cell development arrest and azoospermia in male mice

Liang, Qiu‐Xia ; Wang, Zhen‐Bo ; Lei, Wen‐Long ; Lin, Fei ; Qiao, Jing‐Yi ; Filhol‐Cochet, Odile ; Boldyreff, Brigitte ; Schatten, Heide ; Sun, Qing‐Yuan ; Qian, Wei‐Ping

Cell proliferation, 2020-01, Vol.53 (1), p.e12726-n/a [Periódico revisado por pares]

England: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
9
A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia
A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia

Seabra, Catarina M ; Quental, Sofia ; Neto, Ana Paula ; Carvalho, Filipa ; Gonçalves, João ; Oliveira, João Paulo ; Fernandes, Susana ; Sousa, Mário ; Barros, Alberto ; Amorim, António ; Lopes, Alexandra M

Reproductive biomedicine online, 2014-09, Vol.29 (3), p.388-391 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

Texto completo disponível

Citações Citado por
10
TTY2 genes deletions as genetic risk factor of male infertility
TTY2 genes deletions as genetic risk factor of male infertility
Material Type:
Artigo 		Adicionar ao Meu Espaço

TTY2 genes deletions as genetic risk factor of male infertility

Shaveisi-Zadeh, F ; Alibakhshi, R ; Asgari, R ; Rostami-Far, Z ; Bakhtiari, M ; Abdi, H ; Movafagh, A ; Mirfakhraie, R

Cellular and Molecular Biology, 2017-02, Vol.63 (2), p.57-61 [Periódico revisado por pares]

France

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (69)

Data de Publicação 

De até
Refinar
  1. Antes de1999  (9)
  2. 1999Até2003  (20)
  3. 2004Até2010  (18)
  4. 2011Até2017  (11)
  5. Após 2017  (13)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.