Components of IGF-axis in growth disorders: A systematic review and patent landscape report
Purpose In this review, epi/genetic mutations of IGF-axis components associated with growth
disorders have been summarized alongwith assessment of relevant diagnostic and …
disorders have been summarized alongwith assessment of relevant diagnostic and …
Liver fat metabolism of broilers regulated by Bacillus amyloliquefaciens TL via stimulating IGF-1 secretion and regulating the IGF signaling pathway
P Chen, S Li, Z Zhou, X Wang, D Shi, Z Li, X Li… - Frontiers in …, 2022 - frontiersin.org
Bacillus amyloliquefaciens TL (BA-TL) is well-known for its capability of promoting protein
synthesis and lipid metabolism, in particular, the abdominal fat deposition in broilers …
synthesis and lipid metabolism, in particular, the abdominal fat deposition in broilers …
[HTML][HTML] Mexican case report of a never‐treated Laron syndrome patient evolving to metabolic syndrome, type 2 diabetes, and stroke
I Castilla‐Cortazar, G Femat‐Roldán… - Clinical Case …, 2017 - ncbi.nlm.nih.gov
Laron syndrome (LS) or growth hormone insensitivity (GHI) is a condition given by normal-
high basal GH and low IGF-1 presented with proportionate dwarfism [1]. The metabolic …
high basal GH and low IGF-1 presented with proportionate dwarfism [1]. The metabolic …
Effect of Ethanol Consumption on the Placenta and Liver of Partially IGF-1-Deficient Mice: The Role of Metabolism via CYP2E1 and the Antioxidant Enzyme System
I Martín-Estal, ÓR Fajardo-Ramírez… - Biology, 2022 - mdpi.com
Simple Summary Ethanol is the most consumed drug worldwide, even during pregnancy.
One of its adverse outcomes is fetal growth restriction, an alteration in development due to …
One of its adverse outcomes is fetal growth restriction, an alteration in development due to …
Anemia de Fanconi
A Hernández-Martínez - Medicina interna de México, 2018 - scielo.org.mx
La anemia de Fanconi es una enfermedad hereditaria con patrón de transmisión
autosómico recesivo, asociada con múltiples mutaciones en al menos 20 genes cuyos …
autosómico recesivo, asociada con múltiples mutaciones en al menos 20 genes cuyos …
Fanconi anemia
A Hernández-Martínez - Medicina Interna de México, 2018 - medigraphic.com
Fanconi anemia is a hereditary disease with an autosomal recessive transmission pattern,
associated with multiple mutations on at least 20 genes whose products are part of the cell's …
associated with multiple mutations on at least 20 genes whose products are part of the cell's …
[PDF][PDF] “FACTORES ASOCIADOS CON LA TALLA BAJA, PESO BAJO
FJM PAZ - 2024 - ru.dgb.unam.mx
La Anemia de Fanconi (AF) es un síndrome de inestabilidad cromosómica, principalmente
de herencia autosómica recesiva, por variantes patógenicas en al menos 22 genes …
de herencia autosómica recesiva, por variantes patógenicas en al menos 22 genes …
[HTML][HTML] Diagnosis of Laron syndrome using monoplex-polymerase chain reaction technology with a whole-genome amplification template: A case report
A Neumann, MÁ Alcántara-Ortigoza… - World Journal of …, 2019 - ncbi.nlm.nih.gov
BACKGROUND Laron syndrome (LS) is an autosomal recessive hereditary condition
affecting only 1/1000000 births. The cause is associated with mutations in the growth …
affecting only 1/1000000 births. The cause is associated with mutations in the growth …
Síndrome de larón e inmunidad al cáncer y la diabetes
SC Pin, NV Cedeño, D Callejas - Revista Científica Arbitrada …, 2022 - editorialalema.org
El Síndrome de Laron o Enanismo tipo Laron, también llamado Insensibilidad a la Hormona
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …
del Crecimiento (IGH), es una enfermedad rara, congénita, autosómica recesiva que no …