LE WE PMID CA
LMNA Lamin C Prelamin A9311LMNA Lamin C Prelamin A

Action Myoclonus Renal Failure Syndrome

ACTN4 Alpha actinin4

CD151 Tetraspanin

CD2AP

Charcot Marie Tooth disease type 2b

Coenzyme Q10

Congenital nephrotic syndrome finnish type

COQ2

Denys Drash syndrome

Early onset familial nephrotic syndrome

Emery Dreifuss dystrophy

Epstein s syndrome

Fechtner s syndrome

Frasier s syndrome

Galloway Mowat s syndrome

GMS1

Greenberg HEM dysplasia

Kidney (FSGS)

LAMB2 Laminin beta2

Lamin

Laminin

Laminopathy

Leukodystrophy

Lipodystrophy

Lipodystrphy Dunnigan type

LMNA Lamin C Prelamin A

LMNB1 Lamin B1

LMNB2 Lamin B2

LMX1B

Mandibuloacral dysplasia

May Hegglin anomaly

MYH9

Nail patella syndrome

NPHS1 Nephrin

NPHS2

Pelger Huet anomaly

Phospholipase C epsilon

Pierson s syndrome

PLCE1

Podocin

SCARB2

Schimke immunoosseous dysplasia

Sebastian s syndrome

SMARCALI

Steroid resistant nephrotic syndrome SRN1

TRPC6

WT1

ZMPSTE24

2009  
1
Role of A-type lamins in signaling, transcription, and chromatin organization.
[20038676] J Cell Biol 187(7): 945-57 (2009)
2009  
2
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review.
[19562370] Eur J Pediatr 168(11): 1291-304 (2009)
2009  
3
The posttranslational processing of prelamin A and disease.
[19453251] Annu Rev Genomics Hum Genet 10(-): 153-74 (2009)
2007  
4
"Laminopathies": a wide spectrum of human diseases.
[17467691] Exp Cell Res 313(10): 2121-33 (2007)
2011  
5
Investigating the purpose of prelamin A processing.
[21647293] Nucleus 2(1): 4-9 (2011)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.



  • LMNA Lamin C Prelamin A

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