Matches in Nanopublications for { ?s ?p "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP767508.RAkLjsn2UVdGiIBj-KJJhLB1ZDd6QtmxcWPRyBrMO9_Lk130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767508.RAkLjsn2UVdGiIBj-KJJhLB1ZDd6QtmxcWPRyBrMO9_Lk130_provenance.
- NP653558.RAWXlkMAUqpzWMytoAFte9SbOdmYFgCYW5zz-_VLZpr08130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653558.RAWXlkMAUqpzWMytoAFte9SbOdmYFgCYW5zz-_VLZpr08130_provenance.
- NP180953.RARR576UkwCT0EdJxrqYYMDqvbATYnB5EONas1xvP-HUQ130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180953.RARR576UkwCT0EdJxrqYYMDqvbATYnB5EONas1xvP-HUQ130_provenance.
- NP515125.RAB5FrYtoZxXgTNPLgbpsRlsC2v2OwMxN36hG7gsXMC9c130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515125.RAB5FrYtoZxXgTNPLgbpsRlsC2v2OwMxN36hG7gsXMC9c130_provenance.
- NP383730.RAkazIu8pPJqj-XslF4_OXJ7Cn7GfwUJJJ712D_8ihk6c130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383730.RAkazIu8pPJqj-XslF4_OXJ7Cn7GfwUJJJ712D_8ihk6c130_provenance.
- NP928150.RAWebukSJczM3Houi3CUiQuVumzch1qdPD_g1wSLXVFcU130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP928150.RAWebukSJczM3Houi3CUiQuVumzch1qdPD_g1wSLXVFcU130_provenance.
- NP584818.RAcVh9pyPowfE7TkT-KWv_3J8rCn1l28wJJLTLRTcirmE130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584818.RAcVh9pyPowfE7TkT-KWv_3J8rCn1l28wJJLTLRTcirmE130_provenance.
- assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP754554.RAwZJBkqkb2YA15benGAcvvzUU3INQAKHFI-5gmbQVkE0130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754554.RAwZJBkqkb2YA15benGAcvvzUU3INQAKHFI-5gmbQVkE0130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP670402.RAIyI-ZWUGPNiASn6F0HwdVCKIx6q541f7eEMpmNfp1SA130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670402.RAIyI-ZWUGPNiASn6F0HwdVCKIx6q541f7eEMpmNfp1SA130_provenance.
- NP1356905.RADGV5ZK0sFQt6VMJW5eDedmgVy9X0RtnQk7gA5i1kiGE130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1356905.RADGV5ZK0sFQt6VMJW5eDedmgVy9X0RtnQk7gA5i1kiGE130_provenance.
- NP1356907.RAkZe2w1vGNj8ZmsHhe4rm4dcye9xfcOUDXjeqcsnP_NE130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1356907.RAkZe2w1vGNj8ZmsHhe4rm4dcye9xfcOUDXjeqcsnP_NE130_provenance.
- NP1356908.RAoAJdeFCsEzdRm4HjXSqeiHVJFK41FmHRrFbwnLTaVqw130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1356908.RAoAJdeFCsEzdRm4HjXSqeiHVJFK41FmHRrFbwnLTaVqw130_provenance.
- NP321250.RA4Ek85nmLBp8uSwClKLWvMrqf8jQncf7TmJonewEH1o4130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321250.RA4Ek85nmLBp8uSwClKLWvMrqf8jQncf7TmJonewEH1o4130_provenance.
- NP969311.RAKIqDBgzC974s4lxbRJQnvAnIkLtAl5vZCuTe3u4PWlE130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969311.RAKIqDBgzC974s4lxbRJQnvAnIkLtAl5vZCuTe3u4PWlE130_provenance.
- NP851924.RAIJMDd9ZWsZ7AE0uKf6fpv0Vhj91eQstaXsBQk7a7r84130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851924.RAIJMDd9ZWsZ7AE0uKf6fpv0Vhj91eQstaXsBQk7a7r84130_provenance.
- NP1356904.RA0RWrdPaMteUsU8bVpsU_o2SWw2uAid7wH75VPUbsYHo130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1356904.RA0RWrdPaMteUsU8bVpsU_o2SWw2uAid7wH75VPUbsYHo130_provenance.
- NP1356906.RA4IATbv-wP-9SdLXAbq2OSJWzR4zXZ5OzW79MoBWamQc130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1356906.RA4IATbv-wP-9SdLXAbq2OSJWzR4zXZ5OzW79MoBWamQc130_provenance.