Results 101 to 110 of about 2,703,420 (305)

Y presents the 1952-1953 M Book, Southern Methodist University

open access: yes, 1952
The M Books are a collection of handbooks given to students at Southern Methodist University at the beginning of each year to help them acclimate to campus ...
Young Men's Christian Association (Southern Methodist University); Young Women's Christian Association (Southern Methodist University)
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Expanding the Phenotypic Spectrum of TXNDC15‐Related Ciliopathies to Include Joubert Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic loss‐of‐function variants in TXNDC15 are a known cause of the perinatally lethal ciliopathy Meckel syndrome (MKS). TXNDC15 encodes an endoplasmic reticulum (ER)‐resident thioredoxin‐domain protein required for ciliary transition zone integrity.
Zachary T. Sentell   +16 more
wiley   +1 more source

The M Book, Southern Methodist University, 1959-1960

open access: yes, 1959
The M Books are a collection of handbooks given to students at Southern Methodist University at the beginning of each year to help them acclimate to campus ...
Young Men's Christian Association (Southern Methodist University); Young Women's Christian Association (Southern Methodist University)
core  

Systematic Review of Females With Intellectual Disability and MECP2 Duplication

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT MECP2 Duplication Syndrome (MDS) is a rare, X‐linked neurodevelopmental disorder typically affecting males. Females with MDS have been reported and are compiled here. We conducted a systematic review (PROSPERO CRD420250652426) of PubMed, EMBASE, and Google Scholar extracting individual participant data.
Paul Malik   +10 more
wiley   +1 more source

Trace Elements Genetics: A Potential Role in Treatment‐Resistant Major Psychoses and Related Traits?

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Trace elements are pivotal to key biological processes, with possible effects on psychopathology. We investigated the hypothesis of shared genetic factors between trace elements levels, treatment resistance and related traits. We used genome‐wide summary statistics for trace elements blood concentration, treatment‐resistant depression (TRD ...
Chiara Fabbri   +6 more
wiley   +1 more source

The M Book of Southern Methodist University, 1936-1937

open access: yes, 1936
The M Books are a collection of handbooks given to students at Southern Methodist University at the beginning of each year to help them acclimate to campus ...
Young Men's Christian Association (Southern Methodist University); Young Women's Christian Association (Southern Methodist University)
core  

Southern Educator

open access: yes, 2021
Georgia Southern University accepted as a national partner school for Call Me MISTER® program HPE major makes calls on his future as a coach with support from National Guard Georgia Southern joins Girl Scouts in STEM Education Get to know Dean ...
Georgia Southern University
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The Role of Glutamatergic and Dopaminergic Genes in Resistant Schizophrenia: A Systematic Review

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Psychosis is a heterogeneous disorder, with approximately one‐third of patients experiencing treatment resistance, predominantly among individuals diagnosed with Schizophrenia. Treatment‐resistant schizophrenia (TRS) may stem from a distinct biological signature, involving abnormalities in the dopaminergic and glutamatergic systems.
Maria Teresa Moreno‐Calle   +3 more
wiley   +1 more source

The M Book of Southern Methodist University, 1937-1938

open access: yes, 1937
The M Books are a collection of handbooks given to students at Southern Methodist University at the beginning of each year to help them acclimate to campus ...
Young Men's Christian Association (Southern Methodist University); Young Women's Christian Association (Southern Methodist University)
core  

The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with over 400 genetic and many non‐genetic causes implicated in its prenatal development.
Shahrzad Nematollahi   +20 more
wiley   +1 more source

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