Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy.
about
Microvillous inclusion disease (microvillous atrophy)The bigger the better: determining nephron size in kidneyCordon bleu promotes the assembly of brush border microvilli.Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease.Autophagocytosis of the apical membrane in microvillus inclusion disease.Microtubular organization and its involvement in the biogenetic pathways of plasma membrane proteins in Caco-2 intestinal epithelial cellsStructural and functional lesions in brush border of human polarized intestinal Caco-2/TC7 cells infected by members of the Afa/Dr diffusely adhering family of Escherichia coliA family study of protracted diarrhoea in infancy.Alterations in the establishment and maintenance of epithelial cell polarity as a basis for disease processes.Epithelial cell proliferation in childhood enteropathies.Clinical response to the long acting somatostatin analogue SMS 201-995 in a child with congenital microvillus atrophy.Intestinal brush border revisitedShaping the intestinal brush borderLethal familial protracted diarrhoea.Loperamide in severe protracted diarrhoeaSmall intestinal transplantation for irreversible intestinal failure in childrenNeonatal congenital microvillus atrophyCongenital microvillous atrophy: specific diagnostic features.Intractable ulcerating enterocolitis of infancy.Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and HypertriglyceridemiaMyo5b knockout mice as a model of microvillus inclusion disease.Conditional deletion of beta1 integrins in the intestinal epithelium causes a loss of Hedgehog expression, intestinal hyperplasia, and early postnatal lethality.An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral traffickingModulation of function of sodium-dependent vitamin C transporter 1 (SVCT1) by Rab8a in intestinal epithelial cells: studies utilizing Caco-2 cells and Rab8a knockout miceLoss of MYO5B in mice recapitulates Microvillus Inclusion Disease and reveals an apical trafficking pathway distinct to neonatal duodenum.RAB and RHO GTPases regulate intestinal crypt cell homeostasis and enterocyte function.Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations.Disruption of Rab8a and Rab11a causes formation of basolateral microvilli in neonatal enteropathy.Towards understanding microvillus inclusion disease.Identification of intestinal ion transport defects in microvillus inclusion disease.New Mouse Models for Microvillus Inclusion Disease (MVID): Where Do the Inclusions Come From and Are They Cause or Consequence?Microvillus inclusion disease: specific diagnostic features shown by alkaline phosphatase histochemistry.Defective jejunal brush border membrane sodium/proton exchange in association with lethal familial protracted diarrhoea.Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease.Trafficking Ion Transporters to the Apical Membrane of Polarized Intestinal Enterocytes.MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea.Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease.Loss of HAI-2 in mice with decreased prostasin activity leads to an early-onset intestinal failure resembling congenital tufting enteropathy.Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report
P2860
Q21203045-E1A7B322-46FE-495C-BCDA-551CB3E6FD2AQ27026016-C0E7F3FE-E9C4-43DE-A7E8-858FBE30BBB7Q27305309-F26EBD1F-985E-41F1-9CD9-AAC8D26B8BD0Q30581661-BD409533-1BB9-471A-8118-3906C4C1B73BQ31109538-7659F56E-BAEA-46C7-987E-077DFFDD4D14Q33244760-1AAA5B78-24CE-4312-AD93-3E1847849ADDQ33593013-C94FFB92-987C-4475-9C10-3C6C137D4EBFQ33668503-A2910AE3-B910-412C-A197-09453D5FB3CCQ34239056-97BABFFB-6F56-4EAD-A392-2851E713D0DAQ34410178-85285070-222A-463F-B136-16C0C3EED389Q34532427-D7D18D67-332C-49E8-9F52-FEADF31BCC3FQ34532916-8A8399D1-DF06-4261-8795-5C5058FEF7C7Q34566715-13DE675C-A1A2-4408-9FD4-C34D08B00894Q35114751-C944DBA4-774F-4068-8EA4-0EE9F2A91812Q35117043-7C2AAA04-FFFE-440A-9FB2-5FEE5C1B0BE6Q35160335-AE75BD92-2DD7-475E-BE53-68F4A537E7CDQ35518794-9CB40135-BDF2-43AD-9A88-6CEEC0DEDA3EQ35601691-FFD69CF5-ABDC-414F-85EE-8866C8A0E04CQ35626264-76E83A42-F5C1-4C8A-A3E7-2781C73B07D6Q35710172-7205DDCF-CE1E-4E52-BF30-CACD4B6ED07CQ35880786-B158C2AF-B4EA-4AF2-851D-755313147C2DQ36119027-9B9EC8FE-48D3-4C37-BBF0-E7A00542F763Q36155098-4138E43E-2DB8-45C4-A801-6868EF603CD5Q36539878-887DC26D-6FD0-4C24-BC9B-80A708FC37A3Q36724921-D92556E8-2FE0-435E-82D4-EA416973D5C3Q36997840-89A0190D-553B-46EF-8D1E-DC3F5DE094D1Q38696809-42300A74-1E9B-4258-BCD0-8B3FABE3882AQ38735421-B3F1DF45-06D8-4A68-A2DD-A9122937CF89Q41838926-DB80EFCF-F1A0-4B70-B054-17A70D63155FQ42008380-F1EEC150-A79A-4736-83C3-4EB415B48563Q42364743-913239CA-EC56-421F-BAF3-138461366BBCQ42842272-BBE0E184-F8ED-42F4-A649-9581418B817FQ43219775-FD43BABB-98AB-4E56-9D98-774C045C95A0Q46789322-1B4D8414-A8FB-4803-A214-6ACEFDDF4FE8Q47144215-7B87413E-EF11-4FCC-AD9D-21246D8AEF13Q47269140-320AA5E5-881B-4FC0-8060-F939619335B5Q49546561-B3EB6C4C-569A-4421-9953-190F7067CCABQ52723533-A3BFB898-6F29-4F33-8A2D-6D294A228488Q54948226-7026276B-ECE8-482E-9AE3-8907EF9D1634Q58572571-0A036585-BF94-48CA-B95B-1775310D33C0
P2860
Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy.
description
1978 nî lūn-bûn
@nan
1978 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1978 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1978年の論文
@ja
1978年論文
@yue
1978年論文
@zh-hant
1978年論文
@zh-hk
1978年論文
@zh-mo
1978年論文
@zh-tw
1978年论文
@wuu
name
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@ast
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@en
type
label
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@ast
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@en
prefLabel
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@ast
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@en
P2093
P1433
P1476
Familial enteropathy: a syndro ...... nd hypoplastic villus atrophy.
@en
P2093
P304
P407
P577
1978-11-01T00:00:00Z