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Longer titles found: Transient neonatal diabetes (view), Permanent neonatal diabetes (view)

searching for Neonatal diabetes 21 found (44 total)

ABCC8 (1,238 words) [view diff] exact match in snippet view article find links to article

associated with non-insulin-dependent diabetes mellitus type II (neonatal diabetes), an autosomal dominant disease of defective insulin secretion, and

HYMAI (256 words) [view diff] exact match in snippet view article find links to article

Overexpression of HYMAI and the protein-coding gene PLAG1 causes transient neonatal diabetes mellitus type 1 (TNDM1). Long noncoding RNA Arima T, Drewell RA, Oshimura

MODY 2 (684 words) [view diff] exact match in snippet view article find links to article

earlier and the hyperglycemia is more severe. A form of permanent neonatal diabetes has been caused by homozygous mutations in the GCK gene. George, Doss

PLAGL1 (965 words) [view diff] exact match in snippet view article find links to article

gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes". Hum. Mol. Genet. 9 (3): 453–60. doi:10.1093/hmg/9.3.453. PMID 10655556

ZFP57 (491 words) [view diff] exact match in snippet view article find links to article

repressor. Mutations in the ZFP57 gene may be associated with transient neonatal diabetes mellitus. ENSG00000204644, ENSG00000223858, ENSG00000206510, ENSG00000223852

RFX6 (477 words) [view diff] exact match in snippet view article find links to article

associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall

Kir6.2 (1,212 words) [view diff] exact match in snippet view article find links to article

2007). "Molecular cell biology of KATP channels: implications for neonatal diabetes". Expert Reviews in Molecular Medicine. 9 (21): 1–17. doi:10.1017/S1462399407000403

ATP-sensitive potassium channel (2,575 words) [view diff] case mismatch in snippet view article find links to article

"Targeted Overactivity of β Cell KATP Channels Induces Profound Neonatal Diabetes". Cell. 100 (6): 645–654. doi:10.1016/S0092-8674(00)80701-1. PMID 10761930

Neurogenin-3 (1,280 words) [view diff] exact match in snippet view article find links to article

Genetic mutations in Neurogenin3 have been often found to cause neonatal diabetes and the significance of neurogenin3 has also been further shown using

List of diseases (D) (1,155 words) [view diff] exact match in snippet view article

Developmental coordination disorder Developmental delay epilepsy neonatal diabetes (DEND syndrome) Developmental delay hypotonia extremities hypertrophy

Genomic imprinting (6,485 words) [view diff] exact match in snippet view article find links to article

Silver-Russell syndrome, and pseudohypoparathyroidism. Transient neonatal diabetes mellitus can also involve imprinting. The "imprinted brain hypothesis"

Wolcott–Rallison syndrome (1,002 words) [view diff] case mismatch in snippet view article find links to article

Sreeramaneni, Poorna Gopal Azad., & Ambula, S. R. V. (2017). Ketoacidosis in Neonatal Diabetes Mellitus, Part of Wolcott-Rallison Syndrome. The American Journal

GLIS1 (2,078 words) [view diff] exact match in snippet view article find links to article

insights into their physiological functions and critical roles in neonatal diabetes and cystic renal disease". Histol. Histopathol. 25 (11): 1481–96.

PDX1 (2,449 words) [view diff] case mismatch in snippet view article find links to article

PMID 12124776. S2CID 11530928. GeneReviews/NCBI/NIH/UW entry on Permanent Neonatal Diabetes Mellitus PDX1+protein,+human at the U.S. National Library of Medicine

Beta cell (3,743 words) [view diff] exact match in snippet view article find links to article

pharmacotherapy of ATP-sensitive potassium channel gene mutations underlying neonatal diabetes". Pharmacogenomics and Personalized Medicine. 3: 145–161. doi:10.2147/PGPM

FOXP3 (3,448 words) [view diff] exact match in snippet view article find links to article

McEuen M, Proll S, Appleby M, Brunkow ME (January 2001). "X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent

Inbreeding (7,118 words) [view diff] exact match in snippet view article find links to article

genetic disorders due to inbreeding such as blindness, hearing loss, neonatal diabetes, limb malformations, disorders of sex development, schizophrenia and

Scott Rivkees (2,272 words) [view diff] exact match in snippet view article find links to article

hyperplasia, and the use of thiazide diuretics for the treatment of neonatal diabetes insipidus. For his work in the field of congenital adrenal hyperplasia

Croonian Medal (8,939 words) [view diff] exact match in snippet view article find links to article

development 2013 Frances Ashcroft, From bench to bedside: KATP channels and neonatal diabetes 2012 Tim Bliss, The Mechanics of Memory 2011 John Ellis,Molecular

Mendel Lectures (857 words) [view diff] exact match in snippet view article find links to article

2009 6 41 May 14, 2009 Frances Ashcroft University of Oxford, UK "Neonatal diabetes: From ion channel to disease" 6 42 May 21, 2009 Walter Keller [de]

Developmental bioelectricity (17,264 words) [view diff] case mismatch in snippet view article find links to article

the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes" (PDF). New England Journal of Medicine. 350 (18): 1838–1849. doi:10