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Autism Research : Official Journal of the International Society for Autism Research
|
October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
Neurobiology of Aging
|
September 7, 2023
An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
An Alzheimer's disease risk variant in
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Neurology. Genetics
|
April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease
Martin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Diabetology & Metabolic Syndrome
|
February 12, 2025
Screening and management of hospital hyperglycemia in non-critical patients: a position statement from the Brazilian Diabetes Society (SBD)
Emerson Cestari Marino, Denise Momesso, Marcos Tadashi Kakitani Toyoshima, et al.
Molecular Autism
|
January 14, 2014
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
Holly N Cukier, Nicole D Dueker, Susan H Slifer, et al.
Human Molecular Genetics
|
May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
Anthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
Revista Brasileira De Terapia Intensiva
|
October 14, 2014
Early predictive factors for intensive care unit readmission
André Miguel Japiassú, Michel Schatkin Cukier, Ana Gabriela Coelho de Magalhães Queiroz, et al.
The New England Journal of Medicine
|
June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3
Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
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of 48
Search research articles
Search
Showing results (451-460 of 476) with videos related to
Sort By:
Page
of 48
Autism Research : Official Journal of the International Society for Autism Research
|
October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
Neurobiology of Aging
|
September 7, 2023
An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
An Alzheimer's disease risk variant in
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Neurology. Genetics
|
April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease
Martin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Diabetology & Metabolic Syndrome
|
February 12, 2025
Screening and management of hospital hyperglycemia in non-critical patients: a position statement from the Brazilian Diabetes Society (SBD)
Emerson Cestari Marino, Denise Momesso, Marcos Tadashi Kakitani Toyoshima, et al.
Molecular Autism
|
January 14, 2014
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
Holly N Cukier, Nicole D Dueker, Susan H Slifer, et al.
Human Molecular Genetics
|
May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
Anthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
Revista Brasileira De Terapia Intensiva
|
October 14, 2014
Early predictive factors for intensive care unit readmission
André Miguel Japiassú, Michel Schatkin Cukier, Ana Gabriela Coelho de Magalhães Queiroz, et al.
The New England Journal of Medicine
|
June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3
Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
Page
of 48