skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Base de dados/Biblioteca: Elsevier ScienceDirect Journals remover Base de dados/Biblioteca: PubMed (Medline) remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility
Material Type:
Artigo 		Adicionar ao Meu Espaço

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility

Liu, Chunyu ; Tu, Chaofeng ; Wang, Lingbo ; Wu, Huan ; Houston, Brendan J. ; Mastrorosa, Francesco K. ; Zhang, Wen ; Shen, Ying ; Wang, Jiaxiong ; Tian, Shixiong ; Meng, Lanlan ; Cong, Jiangshan ; Yang, Shenmin ; Jiang, Yiwen ; Tang, Shuyan ; Zeng, Yuyan ; Lv, Mingrong ; Lin, Ge ; Li, Jinsong ; Saiyin, Hexige ; He, Xiaojin ; Jin, Li ; Touré, Aminata ; Ray, Pierre F. ; Veltman, Joris A. ; Shi, Qinghua ; O’Bryan, Moira K. ; Cao, Yunxia ; Tan, Yue-Qiu ; Zhang, Feng

American journal of human genetics, 2021-02, Vol.108 (2), p.309-323 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
2
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia

Whitfield, Marjorie ; Thomas, Lucie ; Bequignon, Emilie ; Schmitt, Alain ; Stouvenel, Laurence ; Montantin, Guy ; Tissier, Sylvie ; Duquesnoy, Philippe ; Copin, Bruno ; Chantot, Sandra ; Dastot, Florence ; Faucon, Catherine ; Barbotin, Anne Laure ; Loyens, Anne ; Siffroi, Jean-Pierre ; Papon, Jean-François ; Escudier, Estelle ; Amselem, Serge ; Mitchell, Valérie ; Touré, Aminata ; Legendre, Marie

American journal of human genetics, 2019-07, Vol.105 (1), p.198-212 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
3
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

Tu, Chaofeng ; Cong, Jiangshan ; Zhang, Qianjun ; He, Xiaojin ; Zheng, Rui ; Yang, Xiaoxuan ; Gao, Yang ; Wu, Huan ; Lv, Mingrong ; Gu, Yayun ; Lu, Shuai ; Liu, Chunyu ; Tian, Shixiong ; Meng, Lanlan ; Wang, Weili ; Tan, Chen ; Nie, Hongchuan ; Li, Dongyan ; Zhang, Huan ; Gong, Fei ; Hu, Liang ; Lu, Guangxiu ; Xu, Wenming ; Lin, Ge ; Zhang, Feng ; Cao, Yunxia ; Tan, Yue-Qiu

American journal of human genetics, 2021-08, Vol.108 (8), p.1466-1477 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
4
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome

Mahyari, Eisa ; Guo, Jingtao ; Lima, Ana C. ; Lewinsohn, Daniel P. ; Stendahl, Alexandra M. ; Vigh-Conrad, Katinka A. ; Nie, Xichen ; Nagirnaja, Liina ; Rockweiler, Nicole B. ; Carrell, Douglas T. ; Hotaling, James M. ; Aston, Kenneth I. ; Conrad, Donald F.

American journal of human genetics, 2021-10, Vol.108 (10), p.1924-1945 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
5
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
Material Type:
Artigo 		Adicionar ao Meu Espaço

SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility

Schilit, Samantha L.P. ; Menon, Shreya ; Friedrich, Corinna ; Kammin, Tammy ; Wilch, Ellen ; Hanscom, Carrie ; Jiang, Sizun ; Kliesch, Sabine ; Talkowski, Michael E. ; Tüttelmann, Frank ; MacQueen, Amy J. ; Morton, Cynthia C.

American journal of human genetics, 2020-01, Vol.106 (1), p.41-57 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
6
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

Dong, Frederick N. ; Amiri-Yekta, Amir ; Martinez, Guillaume ; Saut, Antoine ; Tek, Julie ; Stouvenel, Laurence ; Lorès, Patrick ; Karaouzène, Thomas ; Thierry-Mieg, Nicolas ; Satre, Véronique ; Brouillet, Sophie ; Daneshipour, Abbas ; Hosseini, Seyedeh Hanieh ; Bonhivers, Mélanie ; Gourabi, Hamid ; Dulioust, Emmanuel ; Arnoult, Christophe ; Touré, Aminata ; Ray, Pierre F. ; Zhao, Haiqing ; Coutton, Charles

American journal of human genetics, 2018-04, Vol.102 (4), p.636-648 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
7
Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice
Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice

Dai, Jing ; Zhang, Tianlei ; Guo, Jing ; Zhou, Qinwei ; Gu, Yifan ; Zhang, Jue ; Hu, Liang ; Zong, Yurong ; Song, Juan ; Zhang, Shuoping ; Dai, Can ; Gong, Fei ; Lu, Guangxiu ; Zheng, Wei ; Lin, Ge

American journal of human genetics, 2021-03, Vol.108 (3), p.469-481 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
8
The epidemiology and etiology of azoospermia
The epidemiology and etiology of azoospermia
Material Type:
Artigo 		Adicionar ao Meu Espaço

The epidemiology and etiology of azoospermia

Cocuzza, Marcello ; Alvarenga, Conrado ; Pagani, Rodrigo

Clinics (São Paulo, Brazil), 2013-01, Vol.68 (Suppl 1), p.15-26 [Periódico revisado por pares]

Brazil: Elsevier España, S.L.U

Texto completo disponível

Citações Citado por
9
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

Ben Khelifa, Mariem ; Coutton, Charles ; Zouari, Raoudha ; Karaouzène, Thomas ; Rendu, John ; Bidart, Marie ; Yassine, Sandra ; Pierre, Virginie ; Delaroche, Julie ; Hennebicq, Sylviane ; Grunwald, Didier ; Escalier, Denise ; Pernet-Gallay, Karine ; Jouk, Pierre-Simon ; Thierry-Mieg, Nicolas ; Touré, Aminata ; Arnoult, Christophe ; Ray, Pierre F.

American journal of human genetics, 2014-01, Vol.94 (1), p.95-104 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
10
Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome
Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome

Zhu, Fuxi ; Wang, Fengsong ; Yang, Xiaoyu ; Zhang, Jingjing ; Wu, Huan ; Zhang, Zhou ; Zhang, Zhiguo ; He, Xiaojin ; Zhou, Ping ; Wei, Zhaolian ; Gecz, Jozef ; Cao, Yunxia

American journal of human genetics, 2016-10, Vol.99 (4), p.942-949 [Periódico revisado por pares]

United States: Elsevier Inc

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 (90.118)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (89.328)
  2. magazinearticle  (1.113)
  3. Anais de Congresso  (2)
  4. Mais opções open sub menu

Assunto 

  1. Male  (89.415)
  2. Science & Technology  (75.373)
  3. Life Sciences & Biomedicine  (75.274)
  4. Humans  (64.191)
  5. Female  (55.537)
  6. Animals  (34.016)
  7. Adult  (28.636)
  8. Middle Aged  (28.435)
  9. Aged  (19.850)
  10. Biological And Medical Sciences  (17.681)
  11. Biochemistry & Molecular Biology  (15.979)
  12. Medical Sciences  (14.028)
  13. Rats  (13.381)
  14. General & Internal Medicine  (11.948)
  15. Adolescent  (11.922)
  16. Medicine, General & Internal  (11.691)
  17. Mice  (11.313)
  18. Original  (8.665)
  19. Child  (8.422)
  20. Young Adult  (7.884)
  21. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1960  (162)
  2. 1960Até1975  (2.825)
  3. 1976Até1991  (9.266)
  4. 1992Até2008  (28.325)
  5. Após 2008  (49.890)
  6. Mais opções open sub menu

Idioma 

  1. Inglês  (87.846)
  2. Japonês  (14.678)
  3. Português  (7.672)
  4. Espanhol  (1.732)
  5. Turco  (490)
  6. Lituano  (79)
  7. Francês  (72)
  8. Chinês  (51)
  9. Norueguês  (50)
  10. Alemão  (14)
  11. Russo  (11)
  12. Africâner  (6)
  13. Italiano  (3)
  14. Coreano  (2)
  15. Galês  (1)
  16. Estoniano  (1)
  17. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.