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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Recurrent COPA mutation d" (9 stories)

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Recurrent COPA mutation drives R-spondin-independent Wnt activation in intestinal tumors
Lead StoryNaturegeneral
Jun 12

Recurrent COPA mutation drives R-spondin-independent Wnt activation in intestinal tumors

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9LVUZjZGlSQlpuNnh5TTg0QkltdDdiTzV3QlQyMUVGQXozMGtqTFJpUG1EQzN1Mlg0M1duNTZTOC1jazE2dERJU2hUYVRMZTZKbnd3dnM3blNqanNHU1g4?oc=5" target="_blank">Recurrent COPA mutation drives R-spondin-independent Wnt activation in intestinal tumors</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "Recurrent COPA mutation d"

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8 stories displayed
The STING HAQ haplotype and clinical non-penetrance in COPA syndrome | Journal of Experimental Medicine
Rockefeller University Pressgeneral

The STING HAQ haplotype and clinical non-penetrance in COPA syndrome | Journal of Experimental Medicine

<a href="https://news.google.com/rss/articles/CBMimwFBVV95cUxQcEVRTVRuMHRNQmp1TndrbTVoNVNXbnhId3hicDlkUVlKQjh1VFI0M0txMFd2UVNRd2dyMVhpOW1NZGlPU3ZreG5MMGthSVBucHFNXzJxNGJoc19iRGlXR1d4M0prYnFHM0o3YkJnaGpXNzdpRzA2N1VXVlI3S2lsUkFhZjZCX1hVblJkamZmVk1JNUhNbmszak55Zw?oc=5" target="_blank">The STING HAQ haplotype and clinical non-penetrance in COPA syndrome | Journal of Experimental Medicine</a>  <font color="#6f6f6f">Rockefeller University Press</font>

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New genetic driver found for rare small intestinal cancers
News-Medicalworld

New genetic driver found for rare small intestinal cancers

<a href="https://news.google.com/rss/articles/CBMiqgFBVV95cUxPSE9sT0JVUmtqU3VzQVRYWnljVEtlbmtZWWctdU5jX1NKcWsyYlVpX3BhRUN3LWdLazUxMlBOdFZpMGdPOGRRSm44bm1FZS1FSXY4aHcxZmlSYXNuTXJ2VXlUTWh6Mll0Zzk1Z1VnSmNoRm1ZZ0lTTy1xRHdSd01MQm5oOTN2d0VCSUFYT3J3dkFrSWpYV3JRZWFmQWY4OU91V0phUW01MDZrQQ?oc=5" target="_blank">New genetic driver found for rare small intestinal cancers</a>  <font color="#6f6f6f">News-Medical</font>

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Non-infectious mixed cryoglobulinemia as a new clinical presentation of mutation in the gene encoding coatomer subunit alpha: a case report of two adult sisters
Frontiersworld

Non-infectious mixed cryoglobulinemia as a new clinical presentation of mutation in the gene encoding coatomer subunit alpha: a case report of two adult sisters

<a href="https://news.google.com/rss/articles/CBMikgFBVV95cUxOYlg2Nkh2RVZ5REp2bEd4Y0puTFZ6dWdXUmppSmJfMUIwUWUzaFZZeTNrbzRMcXZhaFRTUVM4azlTSnhqTWJtQm1WeGxKWi1lOVJ2c2M3TnI2VzRITmVERmhfUXlXME5TZ2lrVHVHZWI3Vl9kLUxiMkpMRlltM1Vxc0M1XzhXVm50TzZUbnNpZjI5UQ?oc=5" target="_blank">Non-infectious mixed cryoglobulinemia as a new clinical presentation of mutation in the gene encoding coatomer subunit alpha: a case report of two adult sisters</a>  <font color="#6f6f6f">Frontiers</font>

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Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling
Rockefeller University Pressgeneral

Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

<a href="https://news.google.com/rss/articles/CBMiqAFBVV95cUxPUHNta2llY2h0d2NQYkRjNVhyX1pNaHRWNWxPNTVPNzA3Z3dWT0FyQUtETGxoRW9abzhwRlhPaDFrMFQ1WTVST2Nha2dQTlBrWmU3MGlncXVLazBjT0lrMFVfWTJIT2tEc1I2U2NiQUVHZmtmVk9vcENhekkyNTFtS3pPd3dyWHJQZC04OUV3VklqVXQ3dU0wYXBWUjQwdTZxNzBZV1lTWDU?oc=5" target="_blank">Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling</a>  <font color="#6f6f6f">Rockefeller University Press</font>

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Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species
Naturemarkets

Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9pZjk3V21IYUFMRlJEcnZXZG9FRWhzcENVX1drN2V5V29MdHdmN3RDMDBLZ24wUEhNS0xjdjhubERwMjVNZ1VHMkZkNEpBVTd3aDNRMzRwc0o4RHNkWmZJ?oc=5" target="_blank">Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species</a>  <font color="#6f6f6f">Nature</font>

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Interferonopathies masquerading as non-Mendelian autoimmune diseases: pattern recognition for early diagnosis
Frontiersworld

Interferonopathies masquerading as non-Mendelian autoimmune diseases: pattern recognition for early diagnosis

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxOYk5XOXlCWXh3WmkwRlZKSTBPNzBscnVUMXU1cmJpVlZ1cGFON2h0VVhNRnM0YjNCbmdLaTkwdWhmSVZJQTRYSEprTUFGd1Zid1NqWmt0NzFvbnZ0aGpMMlhVNy12YmNlc09CLUlkY1o1amh3cUU1RTRzZWRfdHRac1hPbndYb0ZEdHRQS3duZTc?oc=5" target="_blank">Interferonopathies masquerading as non-Mendelian autoimmune diseases: pattern recognition for early diagnosis</a>  <font color="#6f6f6f">Frontiers</font>

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A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
Natureworld

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBaenVpTEhwNk0zMzF3RGNkUUVPaHhkbDQ3WEhSa3VuUVFYWW9HTHdrVGpkaDFLOGpBVGlBbnpuY3VnOTJKZWhydUk0VFdMQ252N3BpcHNBWk9pVTJUM1RN?oc=5" target="_blank">A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease</a>  <font color="#6f6f6f">Nature</font>

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Vasculitis in Systemic Autoinflammatory Diseases
Frontiersgeneral

Vasculitis in Systemic Autoinflammatory Diseases

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxNeFRFRlE2TlZMQzNuRHZnQjVBUTZwSWd1UkwtbEhZazV0a3ljeHlERkRaM242RGxRSC1CcUZSdFVuQ1dkLVh2Z2JKT1VRaVNEMTBqeVQ2ODFwaG4ta0gwd0QwR296dUd6S3FEajBaM3RfWkhYd18yQmJ0MmZnS2lPRjA3eG5lajQ3NFRxMWVB?oc=5" target="_blank">Vasculitis in Systemic Autoinflammatory Diseases</a>  <font color="#6f6f6f">Frontiers</font>

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"Recurrent COPA mutation d" — Live Google News Trends & Headlines