About: Biochemical and molecular medicine

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journal

Attributes	Values
rdf:type	Item
description	journal (en) revista científica (es) ساینَسی رِسالہٕ (ks) revue scientifique (fr) rivista scientifica (it) науковий журнал (uk) wissenschaftliche Fachzeitschrift (de) wetenschappelijk tijdschrift van Academic Press (nl)
language of work or name	wds:Q26842007-387C6C79-A279-4D18-9720-E124499B9FE6
language of work or name	English
OpenCitations bibliographic resource ID	wds:Q26842007-8E3D046D-BEB9-4898-866C-0B910A3521FA
Scilit journal ID	wds:Q26842007-16BACB2A-5A35-40B9-9D5C-667FE9476EFE
Crossref journal ID	wds:Q26842007-6890EF46-0D64-41BC-B6A8-EAB560BD3D8E
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1612692
OpenCitations bibliographic resource ID	1612692
Scilit journal ID	784654
Crossref journal ID	699
rdfs:label	Biochemical and molecular medicine (en) Biochemical and molecular medicine (es) Biochemical and molecular medicine (it) Biochemical and molecular medicine (nl) Biochemical and molecular medicine (ast)
skos:prefLabel	Biochemical and molecular medicine (en) Biochemical and molecular medicine (es) Biochemical and molecular medicine (it) Biochemical and molecular medicine (nl) Biochemical and molecular medicine (ast)
name	Biochemical and molecular medicine (en) Biochemical and molecular medicine (es) Biochemical and molecular medicine (it) Biochemical and molecular medicine (nl) Biochemical and molecular medicine (ast)
title	wds:Q26842007-84BB2679-C8DB-4439-985A-27FB39FEAB4F
title	Biochemical and molecular medicine (en)
NLM Unique ID	wds:Q26842007-B902F8AA-2B24-4012-A478-0EAC735518E5
ACNP journal ID	wds:Q26842007-153B29B3-0998-4427-BA2C-956398E3704A wds:Q26842007-9F3D02F6-158C-4F10-95D1-2141E472D9BF
HAL journal ID	wds:Q26842007-BCDEB7A7-A887-46D0-A6AB-936BCB3FA081
NLM Unique ID	9508702
ACNP journal ID	858077 2255241
HAL journal ID	11098
instance of	wds:Q26842007-920D7F0C-DA1E-4500-9A70-1B5EFAEE57A8
instance of	scientific journal
publisher	wds:Q26842007-6B079961-A1C1-4B7E-8FEF-C339A5A9E2D7
publisher	Academic Press
OpenAlex ID	wds:Q26842007-A2531142-EA1F-4126-AE1C-DE87DAB35834
country of origin	wds:Q26842007-59393F76-EE12-4244-AC0A-EA7C1CAFA4A7
official website	wds:Q26842007-AE443533-3FAA-4AEE-A538-0254D068D873 wds:Q26842007-B143107B-DD54-48EB-A4A5-CCEC1600DDAE
OpenAlex ID	V205180022
country of origin	United States of America
official website	http://firstsearch.oclc.org/journal=1077-3150;screen=info;ECOIP http://www.sciencedirect.com/science/journal/10773150
Scopus source ID	wds:Q26842007-F8B834D0-F0AF-46D8-8018-A3FEB28B3F69
ISSN	wds:Q26842007-DD6C30F0-28EE-4052-9425-9F155C68CF33 wds:Q26842007-E7D77A26-981C-4CFF-BE2D-B7B5C8921F02
ISSN-L	wds:Q26842007-A4220026-5C0B-4920-9A7A-2940E139AA9B
indexed in bibliographic review	wds:Q26842007-01E5CBD2-148A-45E6-9B91-117026B58DE1
ISSN	urn:ISSN:1077-3150 urn:ISSN:1095-5577
ISSN-L	http://issn.org/resource/ISSN/1077-3150
Scopus source ID	36344
ISSN	1077-3150 1095-5577
ISSN-L	1077-3150
indexed in bibliographic review	Scopus
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q26842007
is published in of	Abnormal metabolism of mannose in families with carbohydrate-deficient glycoprotein syndrome type 1. Characterization of human proximal tubular cells after hypoxic preconditioning: constitutive and hypoxia-induced expression of heat shock proteins HSP70 (A, B, and C), HSC70, and HSP90. New physiological importance of two classic residual products: carbon monoxide and bilirubin Expression of DAX-1, the gene responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism, in the hypothalamic-pituitary-adrenal/gonadal axis Plasma methylumbelliferyl-tetra-N-acetyl-beta-d-chitotetraoside hydrolase as a parameter during treatment of gaucher patients Growth factor control of growth and epithelial differentiation in embryonic lungs. Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal Isolation and characterization of the murine homolog of the human EXT2 multiple exostoses gene Loss of function mutations in conserved regions of the human arginase I gene Molecular cloning, characterization, and mapping of a full-length cDNA encoding human UDP-galactose 4'-epimerase Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast cultures. Apoptosis and Free Radicals Phenotypic Comparison of an Osteogenesis Imperfecta Type IV Proband with ade Novoα2(I) Gly922 → Ser Substitution in Type I Collagen and an Unrelated Patient with an Identical Mutation Cathepsin K: isolation and characterization of the murine cDNA and genomic sequence, the homologue of the human pycnodysostosis gene Characterization of the N314D allele of human galactose-1-phosphate uridylyltransferase using a yeast expression system Qualitative and quantitative changes in skeletal muscle mtDNA and expression of mitochondrial-encoded genes in the human aging process. Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency Molecular cloning and characterization of rab27a and rab27b, novel human rab proteins shared by melanocytes and platelets Preliminary investigation of the use of dried-blood spots for the assessment of in utero exposure to environmental pollutants Gender differences in serum leptin levels in humans Ouchterlony double immunodiffusion method demonstrates absence of ferritin immunoreactivity in visceral organs from nine patients with Niemann-Pick disease type C. Deficient ferritin immunoreactivity in visceral organs from four patients with Niemann-Pick disease type C Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body mtDNA deletion in a patient with symptoms of mitochondrial cytopathy but without ragged red fibers. A mouse model of galactose-1-phosphate uridyl transferase deficiency Effects of short-chain acyl-CoA dehydrogenase deficiency on development expression of metabolic enzyme genes in the mouse. Expression study of survival motor neuron gene in human fetal tissues. Changes in plasma glucose, insulin, glucagon, catecholamine, and glycogen contents in tissues during development of alloxan diabetes mellitus in rats. Analysis and biochemistry of blood folate

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