Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment. - Wikidata - wikimedia - TriplyDB

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

http://www.wikidata.org/entity/Q37737537

about

The Good and Bad of β-Catenin in Kidney Development and Renal Dysplasia Renal stem cells: fact or science fiction?Early chronic low-level lead exposure produces glomerular hypertrophy in young C57BL/6J mice Deletion of the prorenin receptor from the ureteric bud causes renal hypodysplasia.Nephron number and its determinants in early life: a primer.The number of fetal nephron progenitor cells limits ureteric branching and adult nephron endowment.Unilateral hypoplastic kidney - a novel highly penetrant feature of familial juvenile hyperuricaemic nephropathy.Tight regulation of p53 activity by Mdm2 is required for ureteric bud growth and branching.Congenital anomalies of the kidney and urinary tract: a genetic disorder?Association of BMPR1A polymorphism, but not BMP4, with kidney size in full-term newborns.Mi-2/NuRD is required in renal progenitor cells during embryonic kidney development.Sonographic Growth Charts for Kidney Length in Normal Korean Children: a Prospective Observational Study.Osr1 Interacts Synergistically with Wt1 to Regulate Kidney Organogenesis Chronic kidney disease in children.Renal development in the fetus and premature infant.Integrin-linked Kinase Controls Renal Branching Morphogenesis via Dual Specificity Phosphatase 8.An insertion/deletion ACE polymorphism and kidney size in Polish full-term newborns.Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria.Sonographic evaluation of kidney echogenicity and morphology among HIV sero-positive adults at Lagos University Teaching Hospital.MITF - A controls branching morphogenesis and nephron endowment.SNP Variants in RET and PAX2 and Their Possible Contribution to the Primary Hyperoxaluria Type 1 Phenotype.Chronic kidney disease

P2860

Q26770522-8E10B40C-9AD4-406D-AA2F-EF8F6EF2D3CE Q27006064-5DC9E34C-30FE-4E0F-B9B9-CD3E2E3AAB0F Q28397738-E2577798-FE64-49CA-9EB5-0F453388CF9A Q30419212-01017588-D906-47B4-82A4-3B4EFD803DCF Q30457363-A8BB8C6B-B10B-48EF-BBBE-2D271BB05E2B Q30580163-9544112D-70E8-4DCB-AB98-7ED7E6EA075F Q33678398-473C92BC-F39A-407D-8A69-0FE2940E45B3 Q34915943-6E5F638A-84E8-495D-A302-74E39992D049 Q35997775-DB2D2051-9D29-4089-8E8F-86A837E963C3 Q36563268-C71B41D0-3F84-4460-B9CE-49569C4011B2 Q36706151-6F88D7C2-275E-4AD1-B91D-C2F033F1E39E Q36989800-372B9EAE-B3DA-468F-9A85-B4F0E7D8E60D Q37115114-642A6A2C-E093-439C-A385-C4C4A069C01A Q37119068-9C1905F7-09B2-452C-8644-942816D38C04 Q39119810-F70DB545-F5BC-49C2-9AAC-C278E77B5031 Q40500279-EE3DF919-DA96-4894-A06E-38DEC72CEFCC Q43848638-64582BA0-287D-44BC-82CC-ED10B655498A Q46698056-CC7FFFC7-56B4-4319-AA7E-448F4CE46437 Q47548601-05A6F84E-9DE9-4F05-AF57-6C940C24221D Q49180639-954C0E1D-A08E-4DF9-BA89-13EF79F31532 Q53170036-B9EE7B01-DBCF-46E8-9FA2-602DA86E6E2A Q57701181-F9CCB8DA-26F5-41BD-8F21-41FB5E5FDFA5

P2860

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

http://www.wikidata.org/entity/Q37737537

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on August 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@en

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@nl

type

label

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@en

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@nl

prefLabel

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@en

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@nl

P1433

Q37737537-4B3FDFD1-16CB-400E-8AFA-0055E26F768C

P1476

Q37737537-28E771BD-B033-471B-B533-AF03E6B3BBC9

P2093

Q37737537-64CE73A3-921E-4A1D-91B3-52D7D556FB92

Q37737537-772719A4-EE24-4E34-9560-9104B0B03348

Q37737537-D0DA6E48-5281-4BE5-A118-2B8AA2BAC0C0

Q37737537-F58763A5-C021-41C2-BE75-60BB9362585D

P2860

Q37737537-00AD23F2-0E1E-48C0-A172-1E6A2C031B79

Q37737537-015E5895-9402-419A-AA11-88AC9F5032F2

Q37737537-016BD45E-96C9-461F-AF72-2CC6A6598407

Q37737537-0A898D8D-1CD5-45A2-94E9-4FF2E94079D7

Q37737537-0B15BAA5-6E43-46C0-A748-8B9808A7FB9F

Q37737537-0C7D6A97-D328-4DB7-AB58-A087365577D4

Q37737537-0FBA2531-0349-47DD-8C74-FF8A4EDF7C6A

Q37737537-10B16E39-6E48-46B2-A929-1880B12AF286

Q37737537-1193613A-52C2-4DDB-8BAC-6B7C22901E6E

Q37737537-11FD527E-10D4-46E8-BD25-D50654405808

P2888

Q37737537-D98E8CB7-E710-4BB7-8DE3-32DFC9C3629E

P304

Q37737537-B9322959-ED4C-4D02-AF53-4C547EC83A85

P31

Q37737537-CF8A48B8-CF9E-4A69-A80C-5D955845161B

P356

Q37737537-42D303EA-EA0C-4E9D-BF2A-FF5EC017E81B

P407

Q37737537-826B4E8F-0C52-448C-8169-FF190C8AFD5B

P433

Q37737537-62DD56A9-4D4D-458F-BD2B-8F514DDB199C

P478

Q37737537-783276A1-C0CC-4ADA-91E3-E3CBA68373EC

P577

Q37737537-B41DF24B-9310-4FA6-8984-68556547D699

P6179

Q37737537-0FBBCDFA-A127-4C64-B2A9-97010EE9155D

P698

Q37737537-295B8A94-4E5A-47B3-8265-ACF64B71F681

P356

PDR.0B013E3181E35A88

P1433

Pediatric Research

P1476

Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.

@en

P2093

Jason E Cain

http://www.w3.org/2001/XMLSchema#string

Joanna Smeeton

http://www.w3.org/2001/XMLSchema#string

Norman D Rosenblum

http://www.w3.org/2001/XMLSchema#string

Valeria Di Giovanni

http://www.w3.org/2001/XMLSchema#string

P2860

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

A common variant of the PAX2 gene is associated with reduced newborn kidney size

Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage

Defects in enteric innervation and kidney development in mice lacking GDNF

SIX2 and BMP4 mutations associate with anomalous kidney development

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

Regulation of metanephric kidney development by growth/differentiation factor 11

Renal-coloboma syndrome: prenatal detection and clinical spectrum in a large family

Redefining papillorenal syndrome: an underdiagnosed cause of ocular and renal morbidity

A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis

P2888

pdr.0b013e3181e35a88

P304

91-98

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1203/PDR.0B013E3181E35A88

http://www.w3.org/2001/XMLSchema#string

P407

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

68

http://www.w3.org/2001/XMLSchema#string

P577

2010-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1043288179

http://www.w3.org/2001/XMLSchema#string

P698

20421843

http://www.w3.org/2001/XMLSchema#string