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Molecular and Cellular Pediatrics is a peer-reviewed journal published by Springer Nature, covering Neonatal Respiratory Health Research, Congenital Diaphragmatic Hernia Studies, Infant Nutrition and Health.
| Publisher | Springer Nature |
|---|---|
| Reference style | Numbered (Springer Basic) Numbered — [1], [2] in the text 1. Smith A, Jones B, Lee C (2023) A representative article title. Molecular and Cellular Pediatrics 12:45–58
Formats any DOI in Molecular and Cellular Pediatrics style. No sign-up. |
| Publishes research in | Neonatal Respiratory Health Research Congenital Diaphragmatic Hernia Studies Infant Nutrition and Health Renal and related cancers Cystic Fibrosis Research Advances |
| ISSN | 2194-7791 |
| Citation impact (2-yr) | 1.56 |
| h-index | 40 |
| i10-index | 124 |
| Total citations | 4,775 |
| Article processing charge | $1,704 |
| Open access | Yes |
| Top institutions publishing here | German Center for Lung Research |
| Journal website | molcellped.springeropen.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
The maintenance of oxygen homeostasis in human tissues is mediated by several cellular adaptations in response to low-oxygen stress, called hypoxia. A decrease in tissue oxygen levels is initially counteracted by increasing local blood flow to overcome diminished oxygenation and avoid hypoxic stress. However, studies have shown that the physiological oxygen concentrations in several tissues…
BACKGROUND: The developmental origin of health and disease concept identifies the brain, cardiovascular, liver, and kidney systems as targets of fetal adverse programming with adult consequences. As the limits of viability in premature infants have been pushed to lower gestational ages, the long-term impact of prematurity on kidneys still remains a significant burden during hospital…
Bronchopulmonary dysplasia is a chronic lung disease of preterm infants. It is caused by the disturbance of physiologic lung development mainly in the saccular stage with lifelong restrictions of pulmonary function and an increased risk of abnormal somatic and psychomotor development. The contributors to this disease's entity are multifactorial with pre- and postnatal origin. Central…
Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight distinct mutations found so far in humans.
Inflammatory bowel disease (IBD) is a chronic relapsing inflammatory disease of the intestine. IBD is a multifactorial disorder, and IBD-associated genes are critical in innate immune response, inflammatory response, autophagy, and epithelial barrier integrity. Moreover, epithelial oxygen tension plays a critical role in intestinal inflammation and resolution in IBD. The intestines have a dynamic and…
