skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Base de dados/Biblioteca: PMC (PubMed Central) remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
Material Type:
Artigo 		Adicionar ao Meu Espaço

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

Yatsenko, S A ; Cheung, S W ; Scott, D A ; Nowaczyk, M J M ; Tarnopolsky, M ; Naidu, S ; Bibat, G ; Patel, A ; Leroy, J G ; Scaglia, F ; Stankiewicz, P ; Lupski, J R

Journal of medical genetics, 2005-04, Vol.42 (4), p.328-335 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

Citações Citado por
2
A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?
A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?

Erickson, R.P. ; Yatsenko, S.A. ; Larson, K. ; Cheung, S.W.

Molecular syndromology, 2011-01, Vol.1 (4), p.185-191 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

Texto completo disponível

Citações Citado por
3
The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function
The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function
Material Type:
Artigo 		Adicionar ao Meu Espaço

The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function

Yatsenko, A S ; Kucherenko, M M ; Pantoja, M ; Fischer, K A ; Madeoy, J ; Deng, W-M ; Schneider, M ; Baumgartner, S ; Akey, J ; Shcherbata, H R ; Ruohola-Baker, H

BMC developmental biology, 2009-02, Vol.9 (1), p.18-18, Article 18 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
4
Evaluation of carcinogenic risk in friction product workers
Evaluation of carcinogenic risk in friction product workers
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evaluation of carcinogenic risk in friction product workers

Kogan, P M ; Yatsenko, A S ; Tregubov, E S ; Gurvich, E B ; Kuzina, L E

Medicina del lavoro, 1993-07, Vol.84 (4), p.290

Italy

Sem texto completo

Citações Citado por
5
A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?
A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?
Material Type:
Report 		Adicionar ao Meu Espaço

A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?

Erickson, R P ; Yatsenko, S A ; Larson, K ; Cheung, S W

Molecular syndromology, 2011, Vol.1 (4), p.185-191

Texto completo disponível

Citações Citado por
6
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
Material Type:
Report 		Adicionar ao Meu Espaço

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

Yatsenko, S A ; Cheung, S W ; Scott, D A ; Nowaczyk, M J M ; Tarnopolsky, M ; Naidu, S ; Bibat, G ; Patel, A ; Leroy, J G ; Scaglia, F ; Stankiewicz, P ; Lupski, J R

Journal of medical genetics, 2005, Vol.42 (4), p.328-335

Texto completo disponível

Citações Citado por
7
Distant activation of Notch signaling induces stem cell niche assembly
Distant activation of Notch signaling induces stem cell niche assembly
Material Type:
Artigo 		Adicionar ao Meu Espaço

Distant activation of Notch signaling induces stem cell niche assembly

Yatsenko, Andriy S ; Shcherbata, Halyna R Huynh, Jean-René

PLoS genetics, 2021-03, Vol.17 (3), p.e1009489-e1009489 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
8
Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis
Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis

Shin, Yong-Hyun ; Choi, Youngsok ; Erdin, Serpil Uckac ; Yatsenko, Svetlana A ; Kloc, Malgorzata ; Yang, Fang ; Wang, P Jeremy ; Meistrich, Marvin L ; Rajkovic, Aleksandar Hawley, R. Scott

PLoS genetics, 2010-11, Vol.6 (11), p.e1001190-e1001190 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
9
Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR):  Molecular Cytogenetic Analysis
Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR):  Molecular Cytogenetic Analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR):  Molecular Cytogenetic Analysis

Olszewska, Marta ; Stokowy, Tomasz ; Pollock, Nijole ; Huleyuk, Nataliya ; Georgiadis, Andrew ; Yatsenko, Svetlana ; Zastavna, Danuta ; Yatsenko, Alexander N ; Kurpisz, Maciej

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4559 [Periódico revisado por pares]

Switzerland: MDPI AG

Texto completo disponível

Citações Citado por
10
Med12 gain-of-function mutation causes leiomyomas and genomic instability
Med12 gain-of-function mutation causes leiomyomas and genomic instability
Material Type:
Artigo 		Adicionar ao Meu Espaço

Med12 gain-of-function mutation causes leiomyomas and genomic instability

Mittal, Priya ; Shin, Yong-Hyun ; Yatsenko, Svetlana A ; Castro, Carlos A ; Surti, Urvashi ; Rajkovic, Aleksandar

The Journal of clinical investigation, 2015-08, Vol.125 (8), p.3280-3284 [Periódico revisado por pares]

United States: American Society for Clinical Investigation

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. Recursos Online (131)
  2. Revistas revisadas por pares (119)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (131)
  2. Reports  (3)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de2005  (14)
  2. 2005Até2009  (16)
  3. 2010Até2014  (19)
  4. 2015Até2019  (25)
  5. Após 2019  (61)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.