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Refinado por: tipo de recurso: Outros remover
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1
The role of chromosome 8p deletion in breast cancer development and progression
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The role of chromosome 8p deletion in breast cancer development and progression

Cai, Yanyan

FEBS JOURNAL, 2016, Vol.281, p.510-510

WILEY-BLACKWELL

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2
Identification of novel additional uvrA genes in bacteria
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Identification of novel additional uvrA genes in bacteria

Marszalkowska, Marta ; Bil, Magdalena ; Kreft, Lukasz ; Olszewski, Marcin

2012

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3
Williams-Beuren syndrome: a model of recurrent genomic mutation
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Williams-Beuren syndrome: a model of recurrent genomic mutation

Pérez Jurado, Alberto Luis

Hormone research, 2003, Vol.59 Suppl 1, p.106-113

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4
ZFN-mediated gene disruption of the thyroid hormone activating deiodinase type 2 in zebrafish perturbs male and female reproduction
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ZFN-mediated gene disruption of the thyroid hormone activating deiodinase type 2 in zebrafish perturbs male and female reproduction

Houbrechts, Anne ; Van houcke, Jolien ; Darras, Veerle

2017

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5
Leber congenital amaurosis - a model for efficient genetic testing of heterogeneous disorders: LXIV Edward Jackson Memorial Lecture
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Leber congenital amaurosis - a model for efficient genetic testing of heterogeneous disorders: LXIV Edward Jackson Memorial Lecture

Stone, Edwin M

American journal of ophthalmology, 2007, Vol.144 (6), p.791-811

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6
Neutrophil Peptidylarginine Deiminase 4 is Essential for Detrimental Age-Related Cardiac Remodeling in Mice
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Neutrophil Peptidylarginine Deiminase 4 is Essential for Detrimental Age-Related Cardiac Remodeling in Mice

Van Bruggen, Stijn ; Van Wauwe, Jore ; Carai, Paolo ; Frederix, Liesbeth ; Witsch, Thilo ; Martinod, Kimberly

Circulation, 2021, Vol.144 (Suppl_1)

American Heart Association

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7
A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders
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A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders

Simeoni, Ilenia ; Stephens, Jonathan C ; Hu, Fengyuan ; Deevi, Sri VV ; Megy, Karyn ; Bariana, Tadbir K ; Lentaigne, Claire ; Schulman, Sol ; Sivapalaratnam, Suthesh ; Vries, Minka JA ; Westbury, Sarah K ; Greene, Daniel ; Papadia, Sofia ; Alessi, Marie-Christine ; Attwood, Antony P ; Ballmaier, Matthias ; Baynam, Gareth ; Bermejo, Emilse ; Bertoli, Marta ; Bray, Paul F ; Bury, Loredana ; Cattaneo, Marco ; Collins, Peter ; Daugherty, Louise C ; Favier, Rémi ; French, Deborah L ; Furie, Bruce ; Gattens, Michael ; Germeshausen, Manuela ; Ghevaert, Cedric ; Goodeve, Anne ; Guerrero, Jose ; Hampshire, Daniel J ; Hart, Daniel P ; Heemskerk, Johan WM ; Henskens, Yvonne MC ; Hill, Marian ; Hogg, Nancy ; Jolley, Jennifer D ; Kahr, Walter H ; Kelly, Anne M ; Kerr, Ron ; Kostadima, Myrto ; Kunishima, Shinji ; Lambert, Michele P ; Liesner, Ri ; Lopez, Jose ; Mapeta, Rutendo P ; Mathias, Mary ; Millar, Carolyn M ; Nathwani, Amit ; Neerman-Arbez, Marguerite ; Nurden, Alan T ; Nurden, Paquita ; Othman, Maha ; Peerlinck, Kathelijne ; Perry, David J ; Poudel, Pawan ; Reitsma, Pieter ; Rondina, Matthew ; Smethurst, Peter A ; Stevenson, William ; Szkotak, Artur ; Tuna, Salih ; Van Geet, Chris ; Whitehorn, Deborah ; Wilcox, David A ; Zhang, Bin ; Revel-Vilk, Shoshana ; Gresele, Paolo ; Bellissimo, Daniel ; Penkett, Christopher J ; Laffan, Michael A ; Mumford, Andrew D ; Rendon, Augusto ; Gomez, Keith ; Freson, Kathleen ; Ouwehand, Willem H ; Turro, Ernest

Blood, 2016, Vol.127 (23), p.307-307

W.B. Saunders

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8
The Effects of CDKN1a/p21 on Oxidative Stress and Mitochondrial Function During Long Duration Spaceflight
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The Effects of CDKN1a/p21 on Oxidative Stress and Mitochondrial Function During Long Duration Spaceflight

Stimpel, Olivia ; Almeida, Eduardo ; Blaber, Elizabeth A.

Ames Research Center 2017

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9
High agreement between a cardiology specific scoring system and the ACMG criteria for genetic variant interpretation and classification
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High agreement between a cardiology specific scoring system and the ACMG criteria for genetic variant interpretation and classification

Robyns, Tomas ; Kuiperi, Cuno ; Willems, Rik ; Van Cleemput, Johan ; Nuyens, Dieter ; Breckpot, Jeroen ; Matthijs, Gert ; Corveleyn, Anniek

Circulation, 2016, Vol.134

Lippincott Williams & Wilkins

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10
Permanent deiodinase type 2 deficiency alters local thyroid hormone levels, disturbs development and strongly reduces fertility
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Permanent deiodinase type 2 deficiency alters local thyroid hormone levels, disturbs development and strongly reduces fertility

Houbrechts, Anne ; Delarue, Julie ; Van houcke, Jolien ; Gabriëls, J ; Darras, Veerle

2016

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