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Anna L Mitchell

Showing results (31-40 of 61) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|August 31, 2016
Impact of Month of Birth on the Risk of Development of Autoimmune Addison's DiseaseAgnieszka Pazderska, Marta Fichna, Anna L Mitchell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2013
Ventilatory pattern and energy expenditure are altered in cystic fibrosis miceRebecca J Darrah, Ilya R Bederman, Anna L Mitchell, et al.
Clinical Endocrinology|January 17, 2013
The effect of B cell depletion therapy on anti-TSH receptor antibodies and clinical outcome in glucocorticoid-refractory Graves' orbitopathyAnna L Mitchell, Earn H Gan, Margaret Morris, et al.
Genes|April 23, 2022
Identification of a Cancer-Predisposing Germline <i>POT1</i> p.Ile49Metfs*7 Variant by Targeted Sequencing of a Splenic Marginal Zone LymphomaAudrey N Jajosky, Anna L Mitchell, Mahmut Akgul, et al.
The Journal of Clinical Endocrinology and Metabolism|April 18, 2020
Natural History of Adrenal Steroidogenesis in Autoimmune Addison's Disease Following Diagnosis and TreatmentCatherine Napier, Kathleen Allinson, Earn H Gan, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2016
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in HumansAgnieszka Pazderska, Bergithe E Oftedal, Catherine M Napier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2012
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationshipsKristen Lipscomb Sund, Sarah L Zimmerman, Cameron Thomas, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|October 24, 2009
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibilityAnna L Mitchell, Heather J Cordell, Rachel Soemedi, et al.
The FEBS Journal|July 13, 2005
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Endocrinology and Metabolism|August 31, 2016
Impact of Month of Birth on the Risk of Development of Autoimmune Addison's DiseaseAgnieszka Pazderska, Marta Fichna, Anna L Mitchell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2013
Ventilatory pattern and energy expenditure are altered in cystic fibrosis miceRebecca J Darrah, Ilya R Bederman, Anna L Mitchell, et al.
Clinical Endocrinology|January 17, 2013
The effect of B cell depletion therapy on anti-TSH receptor antibodies and clinical outcome in glucocorticoid-refractory Graves' orbitopathyAnna L Mitchell, Earn H Gan, Margaret Morris, et al.
Genes|April 23, 2022
Identification of a Cancer-Predisposing Germline <i>POT1</i> p.Ile49Metfs*7 Variant by Targeted Sequencing of a Splenic Marginal Zone LymphomaAudrey N Jajosky, Anna L Mitchell, Mahmut Akgul, et al.
The Journal of Clinical Endocrinology and Metabolism|April 18, 2020
Natural History of Adrenal Steroidogenesis in Autoimmune Addison's Disease Following Diagnosis and TreatmentCatherine Napier, Kathleen Allinson, Earn H Gan, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2016
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in HumansAgnieszka Pazderska, Bergithe E Oftedal, Catherine M Napier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2012
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationshipsKristen Lipscomb Sund, Sarah L Zimmerman, Cameron Thomas, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|October 24, 2009
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibilityAnna L Mitchell, Heather J Cordell, Rachel Soemedi, et al.
The FEBS Journal|July 13, 2005
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.
Pageof 7