Results 71 to 80 of about 5,333,786 (244)
Animals, 2020 The aim of this research was to evaluate the effect of biochar diet supplementation for broiler chickens on (1) ammonia and odor emissions from manure, (2) feed conversion ratio and daily weight gain, and (3) selected meat quality and sensory parameters.
Kajetan Kalus +4 more
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Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Benign hyperphenylalaninemia (bHPA) is defined as elevated phenylalanine (Phe) levels remaining ≤ 360 μmol/L (6 mg/dL) and not requiring medical intervention. Individuals with bHPA may demonstrate a rise in their Phe levels > 360 μmol/L, effectively developing a mild PKU phenotype requiring therapy to prevent neurocognitive complications. This
Aaron Williams +8 more
wiley +1 more source
A Mitochondrial Basis for Casein-Induced Inflammation: Haplogroups J & K Susceptibility to BCM‑7
This white paper introduces the Queen Hypothesis, a novel theory proposing that individuals with mitochondrial haplogroups J and K are uniquely sensitive to BCM‑7, an inflammatory peptide released during digestion of A1 dairy. Drawing from mitochondrial genetics, nutritional science, and peptide biochemistry, the paper explains how this sensitivity may
openaire +4 more sources
IMPACT OF RENAL TRANSPLANTATION ON BODY COMPOSITION
Kidney Research and Clinical Practice, 2012 The aim of the study was to analyse the impact of renal transplantation on body composition (Body Cell Mass) in adult kidney transplant recipients.Body Cell Mass (BCM) was calculated from total body potassium (TBK), determined from K-40 in a whole body ...
AC Johansson +4 more
doaj +1 more source
A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco +6 more
wiley +1 more source
Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston +6 more
wiley +1 more source
Journal of Agriculture and Food ResearchThis study explores the proteolytic changes and volatile organic compound (VOC) profiles occurring during the ripening of Mediterranean buffalo milk blue cheese.The main objective was to characterize bioactive peptides, casein phosphopeptides, and ...
Federica Della Cerra +9 more
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Bipartite connectivity mapping (BCM)
, 2020 Introduction: Here we present a new approach called ``Bipartite connectivity mapping (BCM)'' for analyzing connectivity in rs-fMRI between two brain regions. The two regions can be of any size, but should be non-overlapping. The main idea is to represent
Scheffler, K., Lohmann, G., Stelzer, J.
core
Body Composition Analysis of the Effect of Water Load Parameters on Prognosis of Patients with Different Modes of Dialysis: a Multicenter Prospective Cohort Study [PDF]
Zhongguo quanke yixueBackground Maintenance hemodialysis (MHD) and peritoneal dialysis (PD) are main treatment methods for uremic patients. It remains an important content of clinical research on better developing treatment protocols to address overhydration (OH) in dialysis
ZHANG Dongliang, MA Yingchun, REN Jianwei, WANG Lei, ZHAO Jingxin, LIN Xuya
doaj +1 more source