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Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis
Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis
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Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis

van Hattem, W A ; Brosens, L A A ; de Leng, W W J ; Morsink, F H ; Lens, S ; Carvalho, R ; Giardiello, F M ; Offerhaus, G J A

Gut, 2008-05, Vol.57 (5), p.623-627 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and British Society of Gastroenterology

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2
Zoonotic transmission of Teladorsagia circumcincta and Trichostrongylus species in Guilan province, northern Iran: molecular and morphological characterizations
Zoonotic transmission of Teladorsagia circumcincta and Trichostrongylus species in Guilan province, northern Iran: molecular and morphological characterizations
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Zoonotic transmission of Teladorsagia circumcincta and Trichostrongylus species in Guilan province, northern Iran: molecular and morphological characterizations

Ashrafi, Keyhan ; Sharifdini, Meysam ; Heidari, Zahra ; Rahmati, Behnaz ; Kia, Eshrat Beigom

BMC infectious diseases, 2020-01, Vol.20 (1), p.28-28, Article 28 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Behavioral characterization of cereblon forebrain-specific conditional null mice: A model for human non-syndromic intellectual disability
Behavioral characterization of cereblon forebrain-specific conditional null mice: A model for human non-syndromic intellectual disability
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Behavioral characterization of cereblon forebrain-specific conditional null mice: A model for human non-syndromic intellectual disability

Rajadhyaksha, Anjali M. ; Ra, Stephen ; Kishinevsky, Sarah ; Lee, Anni S. ; Romanienko, Peter ; DuBoff, Mariel ; Yang, Chingwen ; Zupan, Bojana ; Byrne, Maureen ; Daruwalla, Zeeba R. ; Mark, Willie ; Kosofsky, Barry E. ; Toth, Miklos ; Higgins, Joseph J.

Behavioural brain research, 2012-01, Vol.226 (2), p.428-434 [Periódico revisado por pares]

Shannon: Elsevier B.V

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4
The F508del Mutation in Cystic Fibrosis Transmembrane Conductance Regulator Gene Impacts Bone Formation
The F508del Mutation in Cystic Fibrosis Transmembrane Conductance Regulator Gene Impacts Bone Formation
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The F508del Mutation in Cystic Fibrosis Transmembrane Conductance Regulator Gene Impacts Bone Formation

Le Henaff, Carole ; Gimenez, Annelise ; Haÿ, Eric ; Marty, Caroline ; Marie, Pierre ; Jacquot, Jacky

The American journal of pathology, 2012-05, Vol.180 (5), p.2068-2075 [Periódico revisado por pares]

Bethesda, MD: Elsevier Inc

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5
Single-cell methylomes identify neuronal subtypes and regulatory elements in mammalian cortex
Single-cell methylomes identify neuronal subtypes and regulatory elements in mammalian cortex
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Single-cell methylomes identify neuronal subtypes and regulatory elements in mammalian cortex

Luo, Chongyuan ; Keown, Christopher L. ; Kurihara, Laurie ; Zhou, Jingtian ; He, Yupeng ; Li, Junhao ; Castanon, Rosa ; Lucero, Jacinta ; Nery, Joseph R. ; Sandoval, Justin P. ; Bui, Brian ; Sejnowski, Terrence J. ; Harkins, Timothy T. ; Mukamel, Eran A. ; Behrens, M. Margarita ; Ecker, Joseph R.

Science (American Association for the Advancement of Science), 2017-08, Vol.357 (6351), p.600-604 [Periódico revisado por pares]

United States: American Association for the Advancement of Science

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6
Genetic Determinants of the Gut Microbiome in UK Twins
Genetic Determinants of the Gut Microbiome in UK Twins
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Genetic Determinants of the Gut Microbiome in UK Twins

Goodrich, Julia K. ; Davenport, Emily R. ; Beaumont, Michelle ; Jackson, Matthew A. ; Knight, Rob ; Ober, Carole ; Spector, Tim D. ; Bell, Jordana T. ; Clark, Andrew G. ; Ley, Ruth E.

Cell host & microbe, 2016-05, Vol.19 (5), p.731-743 [Periódico revisado por pares]

United States: Elsevier Inc

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7
A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance
A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance
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A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance

Anderson, Douglas M. ; Anderson, Kelly M. ; Chang, Chi-Lun ; Makarewich, Catherine A. ; Nelson, Benjamin R. ; McAnally, John R. ; Kasaragod, Prasad ; Shelton, John M. ; Liou, Jen ; Bassel-Duby, Rhonda ; Olson, Eric N.

Cell, 2015-02, Vol.160 (4), p.595-606 [Periódico revisado por pares]

United States: Elsevier Inc

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8
One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering
One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering
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One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering

Wang, Haoyi ; Yang, Hui ; Shivalila, Chikdu S. ; Dawlaty, Meelad M. ; Cheng, Albert W. ; Zhang, Feng ; Jaenisch, Rudolf

Cell, 2013-05, Vol.153 (4), p.910-918 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Circular RNAs are abundant, conserved, and associated with ALU repeats
Circular RNAs are abundant, conserved, and associated with ALU repeats
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Circular RNAs are abundant, conserved, and associated with ALU repeats

Jeck, William R ; Sorrentino, Jessica A ; Wang, Kai ; Slevin, Michael K ; Burd, Christin E ; Liu, Jinze ; Marzluff, William F ; Sharpless, Norman E

RNA (Cambridge), 2013-02, Vol.19 (2), p.141-157 [Periódico revisado por pares]

United States: Cold Spring Harbor Laboratory Press

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10
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Stephens, Jonathan ; Dewhurst, Eleanor ; Malka, Samantha ; Plagnol, Vincent ; Rizzo, Roberta ; Scott, Richard H. ; Henderson, Robert H.H. ; MacLaren, Robert E. ; Paterson, Joan ; Aitman, Timothy ; Ali, Sonia ; Ambegaonkar, Gautum ; Arno, Gavin ; Astle, William ; Attwood, Antony ; Bennett, David ; Bitner-Glindzicz, Maria ; Bleda, Marta ; Boggard, Harm ; Carss, Keren ; Clements-Brod, Naomi ; DaCosta, Rosa ; De Vries, Minka ; Dewhurst, Eleanor ; Drewe, Elizabeth ; Egner, William ; Erber, Wendy N. ; Everington, Tamara ; Fletcher, Debra ; Freson, Kathleen ; Gale, Daniel ; Ghali, Neeti ; Ghurye, Rohit ; Gräf, Stefan ; Greene, Daniel ; Grigoriadou, Sofia ; Grozeva, Detelina ; Hackett, Scott ; Hadinnapola, Charaka ; Hague, Rosie ; Hammerton, Tracey ; Heemskerk, Johan W.M. ; Holder, Muriel ; Holder, Susan ; Huissoon, Aarnoud ; Hurst, Jane ; Jolles, Stephen ; Keeling, David ; Kennedy, Fiona ; Kiely, David ; Lawrie, Allan ; Lear, Sara ; Lees, Melissa ; Lentaigne, Claire ; Lorenzo, Lorena ; Mangles, Sarah ; Mapeta, Rutendo ; Masati, Larahmie ; Mathias, Mary ; Michaelides, Michel ; Millar, Carolyn M. ; Moledina, Shahin ; Moore, Anthony ; Murng, Sai ; Oksenhendler, Eric ; Park, Soo-Mi ; Patch, Chris ; Paterson, Joan ; Penkett, Christopher J. ; Pepke-Zaba, Joanna ; Pollock, Val ; Qasim, Waseem ; Quinti, Isabella ; Reid, Evan ; Rondina, Matthew ; Rosser, Elisabeth ; Santra, Saikat ; Sargur, Ravishankar ; Savic, Sinisa ; Scully, Marie ; Sewell, Carrock ; Smith, Kenneth ; Southgate, Laura ; Stauss, Hans ; Stein, Penelope ; Talks, Kate ; Thomas, Ellen ; Thrasher, Adrian ; Tischkowitz, Marc ; Titterton, Catherine ; Turro, Ernest ; von Ziegenweldt, Julie ; Vonk Noordegraaf, Anton ; Wakeling, Emma ; Wanjiku, Ivy ; Welch, Steve ; Westbury, Sarah ; Woods, Geoffrey ; Yong, Patrick ; Webster, Andrew R.

American journal of human genetics, 2017-01, Vol.100 (1), p.75-90 [Periódico revisado por pares]

United States: Elsevier Inc

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