Unusual molecular findings in Kindler syndrome.

Unusual molecular findings in Kindler syndrome.

Item
http://www.wikidata.org/entity/Q36940048
Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 casesKindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferationEmergence and subsequent functional specialization of kindlins during evolution of cell adhesiveness.Sporadic Kindler syndrome with a novel mutation.Kindling the flame of integrin activation and function with kindlinsKindler syndrome: extension of FERMT1 mutational spectrum and natural history.Pseudoainhum in a patient with tuberous sclerosis complex: a case report and review of the literature.Kindler syndrome: a close mimic of dyskeratosis congenita and the need to distinguish the two clinical entities.Of Kindlins and CancerColocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome.Cutaneous and laryngeal squamous cell carcinoma in mixed epidermolysis bullosa, kindler syndrome.KIND1 Loss Sensitizes Keratinocytes to UV-Induced Inflammatory Response and DNA Damage.Updates from the British Society for Investigative Dermatology Annual Meeting, 16-18 April 2007, Nottingham, U.K.
P2860

Unusual molecular findings in Kindler syndrome.

Item
http://www.wikidata.org/entity/Q36940048
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Unusual molecular findings in Kindler syndrome.
@en
type
label
Unusual molecular findings in Kindler syndrome.
@en
prefLabel
Unusual molecular findings in Kindler syndrome.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P356
P1433
P1476
Unusual molecular findings in Kindler syndrome.
@en
P2093
P2860
P304
P31
P356
10.1111/J.1365-2133.2007.08159.X
P407
P433
P478
P577
P5875
P698