نتائج البحث - "Erika Yeh"

1

دورية أكاديمية

Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.

المؤلفون: Ileena Mitra, Alinoë Lavillaureix, Erika Yeh, Michela Traglia, Kathryn Tsang, Carrie E Bearden, Katherine A Rauen, Lauren A Weiss

المصدر: PLoS Genetics, Vol 13, Iss 1, p e1006516 (2017)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5226683?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/244323ab57a34b9ba5dd3e237151395a

Find this article in full text from ProQuest

Full Text Finder

2

دورية أكاديمية

COL18A1 is highly expressed during human adipocyte differentiation and the SNP c.1136C > T in its 'frizzled' motif is associated with obesity in diabetes type 2 patients

المؤلفون: Flavia I.V. Errera, Luís H. Canani, Erika Yeh, Érika Kague, Lucia M. Armelin-Corrêa, Oscar T. Suzuki, Balduíno Tschiedel, Maria Elizabeth R. Silva, Andréa L. Sertié, Maria Rita Passos-Bueno

المصدر: Anais da Academia Brasileira de Ciências, Vol 80, Iss 1, Pp 167-177 (2008)

مصطلحات موضوعية: COL18A1, obesidade, adipogênese, endostatina, frizzled, obesity, adipogenesis, endostatin, Science

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652008000100012; https://doaj.org/toc/0001-3765; https://doaj.org/toc/1678-2690

URL الوصول: https://doaj.org/article/87cbf7807df54e23ad4791e815f34359

Full Text Finder

3

دورية أكاديمية

Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.

المؤلفون: Erika Yeh, Roberto D Fanganiello, Daniele Y Sunaga, Xueyan Zhou, Gregory Holmes, Katia M Rocha, Nivaldo Alonso, Hamilton Matushita, Yingli Wang, Ethylin W Jabs, Maria Rita Passos-Bueno

المصدر: PLoS ONE, Vol 8, Iss 4, p e60439 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3617104?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/435ec9e34bab4c81adb65d7519318ea8

Find this article in full text from ProQuest

Full Text Finder

4

دورية أكاديمية

Deletion of the basement membrane heparan sulfate proteoglycan type XVIII collagen causes hypertriglyceridemia in mice and humans.

المؤلفون: Joseph R Bishop, Maria Rita Passos-Bueno, Loren Fong, Kristin I Stanford, Jon C Gonzales, Erika Yeh, Stephen G Young, Andre Bensadoun, Joseph L Witztum, Jeffrey D Esko, Karen S Moulton

المصدر: PLoS ONE, Vol 5, Iss 11, p e13919 (2010)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC2978080?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/c6874896f581450091c9994b4deff930

Find this article in full text from ProQuest

Full Text Finder

5

Proceedings of the fifth international RASopathies symposium: When development and cancer intersect

المصدر: American Journal of Medical Genetics Part A. 176:2924-2929

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4c9efc4ac4581e8dcdbb0bb1fa168b24
https://doi.org/10.1002/ajmg.a.40632

View record at Wiley

6

Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment

المؤلفون: Santoshi M. Kandalam, Zhi Y. Wu, Lauren A. Weiss, Erik M. Ullian, Katherine A. Rauen, Wandong Zhang, Curtis Tom, Robert Krencik, Dang Q. Dao, Federico M. Camacho, Erika Yeh

المصدر: Molecular Psychiatry. 23:1687-1698

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d201daf21a38ce7cf9d8f3748d2ac506
https://doi.org/10.1038/mp.2017.238

Find this article in full text from Springer Verlag.

Find this article in full text from ProQuest

7

If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism

المؤلفون: Lauren A. Weiss, Erika Yeh

المصدر: Molecular and cellular probes. 30(6)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98cc3cf966ceeeb4d9de4f42c2ba1c49
https://pubmed.ncbi.nlm.nih.gov/27751841

View record from ScienceDirect

8

Cell Type-Dependent Nonspecific Fibroblast Growth Factor Signaling in Apert Syndrome

المؤلفون: Rodrigo Atique, Roberto D. Fanganiello, Felipe Augusto André Ishiy, Daniele Yumi Sunaga, Maria Rita Passos-Bueno, Erika Yeh

المصدر: Stem cells and development. 25(16)

مصطلحات موضوعية: 0301 basic medicine, Fibroblast Growth Factor 9, Cellular differentiation, Biology, Fibroblast growth factor, Bone morphogenetic protein, 03 medical and health sciences, 0302 clinical medicine, Osteogenesis, Animals, Humans, Gene Regulatory Networks, Rats, Wistar, Receptor, Fibroblast Growth Factor, Type 2, Cell Proliferation, FGF10, Fibroblast growth factor receptor 2, Fibroblast growth factor receptor 1, Gene Expression Profiling, Cell Differentiation, Mesenchymal Stem Cells, Cell Biology, Hematology, Fibroblast growth factor receptor 4, Fibroblast growth factor receptor 3, Acrocephalosyndactylia, Cell biology, 030104 developmental biology, 030220 oncology & carcinogenesis, Immunology, Bone Morphogenetic Proteins, Mutation, Fibroblast Growth Factor 10, Developmental Biology, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cedcb70853d8b03f7c3491dc1833a63f
https://pubmed.ncbi.nlm.nih.gov/27339175

9

Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome

المؤلفون: Lauren A. Weiss, Katherine A. Rauen, Erika Yeh, Gemma E. Rooney, Jeroen P. Roose, Ophir D. Klein, Erik M. Ullian, Claude M. Schofield, Philippe Depeille, Amnon Sharir, Alice F. Goodwin

المصدر: The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 36, iss 1

مصطلحات موضوعية: 0301 basic medicine, Male, Autism, Cellular differentiation, Regenerative Medicine, Medical and Health Sciences, Costello syndrome, Neural Stem Cells, Stem Cell Research - Nonembryonic - Human, 2.1 Biological and endogenous factors, Aetiology, Induced pluripotent stem cell, Child, Cells, Cultured, Pediatric, Cultured, Stem Cell Research - Induced Pluripotent Stem Cell - Human, General Neuroscience, Costello Syndrome, Cell Differentiation, Articles, Middle Aged, Neural stem cell, Up-Regulation, iPS cells, Mental Health, Child, Preschool, Neurological, Stem Cell Research - Nonembryonic - Non-Human, Female, Stem cell, Adult, Neurite, Adolescent, Cells, Intellectual and Developmental Disabilities (IDD), Induced Pluripotent Stem Cells, Biology, 03 medical and health sciences, Directed differentiation, stem cells, medicine, Humans, cortical development, Preschool, Neurology & Neurosurgery, Stem Cell Research - Induced Pluripotent Stem Cell, Psychology and Cognitive Sciences, Neurosciences, Infant, Stem Cell Research, medicine.disease, Brain Disorders, Developmental disorder, 030104 developmental biology, ras Proteins, Neuroscience, Ras

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c33826688773ee032bb9b125ac8a7e4
https://europepmc.org/articles/PMC4701956/

10

Estudo da contribuição molecular e celular do periósteo na craniossinostose da síndrome de Apert

المؤلفون: Erika Yeh

المساهمون: Maria Rita dos Santos e Passos Bueno, Hugo Aguirre Armelin, Andrea Laurato Sertie Santos, Tatiana Teixeira Torres, Chao Yun Irene Yan

المصدر: Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05394abd27228d4b3a3f8fe6401d67d3
https://doi.org/10.11606/t.41.2011.tde-24102011-095337

تنقيح النتائج