Results 111 to 120 of about 3,769,336 (261)

Atribuições do Ministério Público Federal

Boletim IBCCRIM
Agravo interno. Recurso extraordinário com agravo. Atribuições do ministério público federal. Controle externo da atividade policial. Art. 129, vii, da constituição federal.
Ministério Público Federal (MPF)
doaj  

Comparative Susceptibility of Donkey and Horse Sperm to Liquid-Storage Temperature. [PDF]

Reprod Domest Anim
Vallejo-Soto P, González Ariza A, Vilela BRN, Montero-Palma C, Rodríguez González-Miranda R, Pérez-Aguilera V, Crespo-Castejón F, Hidalgo M, Dorado J, Ortiz I.   +9 more
europepmc   +1 more source

TTC21B: From Modifier to Causative Gene in Joubert Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic pathogenic variants in TTC21B, encoding the retrograde intraflagellar transport protein IFT139, are a known cause of renal and skeletal ciliopathies. Single heterozygous variants in this gene were found to be enriched in a cohort of patients with various ciliopathy phenotypes, including three individuals with Joubert syndrome (JS), a
Valentina Serpieri, Fulvio D'Abrusco, Anna Pichiecchio, Thouraya Ben Younes, Ichraf Kraoua, Enza Maria Valente   +5 more
wiley   +1 more source

Diastereodivergent Morita-Baylis-Hillman Reaction of α,β-Unsaturated N-tert-Butanesulfinyl Imines and Trifluoromethyl Ketones. [PDF]

J Org Chem
Sirvent A, Blanco-López E, Nájera C, Yus M, Foubelo F, Sansano JM, Retamosa MG.   +6 more
europepmc   +1 more source

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Van Maldergem syndrome (VMLDS) is an ultra‐rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes.
Gabriela Roldão Correia‐Costa, Bruna Fagundes Rodrigues Alaite, Vera Lúcia Gil‐da‐Silva‐Lopes, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Cinnamaldehyde as a Natural Antimicrobial in Donkey Semen: Efficacy and Sperm Cytotoxicity. [PDF]

Reprod Domest Anim
Montero-Palma C, Romero-Salmoral A, Vallejo-Soto P, Vilela BRN, Pérez V, Crespo-Castejón F, Ortiz I, Hidalgo M, Dorado J, Luque I, Gómez-Gascón L.   +10 more
europepmc   +1 more source

Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos, Natasha Monte, Kaio Evandro Cardoso Aguiar, Rita de Cássia Calderaro, Aline Pasquini Santos, Juliana Carla Gomes Rodrigues, André Maurício Ribeiro‐Dos‐Santos, Sandro José De Souza, Ândrea Ribeiro‐Dos‐Santos, João Farias Guerreiro, Sidney Emanuel Batista Dos Santos, Ney Pereira Carneiro Dos Santos   +11 more
wiley   +1 more source

Definição de casos de aids em crianças

DST, 2022
MINISTÉRIO DA SAÚDE
doaj  

The crystalline style of molluscs: the nonlinear dynamics of a macroscale rotating structure in biology. [PDF]

J R Soc Interface
Testón-Martínez S, Lavictoire L, Checa AG, Sainz-Díaz CI, Cartwright JHE.   +4 more
europepmc   +1 more source

Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa, Leandro Rodrigo Ribeiro, Jéssica Lorena Bariviera, Mauro Schneider Oliveira   +3 more
wiley   +1 more source