646 results on '"Kunkel L"'
Search Results
102. Phase I experience with an anti-glycotope monoclonal antibody, RAV12, in recurrent adenocarcinoma
103. Anti-EpCAM XmAb antibodies with improved cytotoxicity
104. A humanizedaAnti-CD40 monoclonal antibody (SGN-40) demonstrates antitumor activity in non-Hodgkin’s lymphoma: Initiation of a phase I clinical trial
105. δ-Sarcoglycan is required for early zebrafish muscle organization
106. Isolation of mouse X-chromosome specific DNA from an X-enriched lambda phage library derived from flow sorted chromosomes
107. Molecular profiles of inflammatory myopathies
108. The molecular genetics of muscular dystrophy
109. Assignment of Nemaline Myopathy (Mim 161800, Nem1) to Chromosome-1
110. High-dose chemotherapy followed by reinfusion of selected CD34+ peripheral blood cells in patients with poor-prognosis breast cancer: a randomized multicentre study
111. IMMUNOCYTOCHEMISTRY IN LIMB-GIRDLE DYSTROPHY WITH IDENTIFIED SARCOGLYCAN MUTATIONS
112. LGMD 2E in Tunisia is caused by a missense mutation Arg91Leu in β-sarcoglycan
113. Cost-Effective Nutritional Interventions in a Chronic Disease Facility
114. α SARCOGLYCAN DEFICIENCY, TWO NOVEL MUTATIONS
115. Molecular characterization of Br-cadherin, a developmentally regulated, brain-specific cadherin
116. A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions
117. Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing.
118. Caregiver financial distress, depressive symptoms and limited social capital as barriers to children's dental care in a mid-western county in the United States.
119. Syntrophin binds to an alternatively spliced exon of dystrophin.
120. Search for torsion dystonia gene
121. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
122. Calculated, measured and actual calories provided to enterally fed, chronic ventilator dependant patients
123. Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.
124. Highlights in Chronic Lymphocytic Leukemia.
125. Dystrophin analysis in idiopathic dilated cardiomyopathy.
126. The giant Duchenne muscular dystrophy gene and its protein product
127. The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain.
128. Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.
129. The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle.
130. Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.
131. Dystrophin is transcribed in brain from a distant upstream promoter.
132. Identification of a chromosome 6-encoded dystrophin-related protein.
133. Enormous dystrophin in a patient with Becker muscular dystrophy
134. Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility.
135. Improved diagnosis of Duchenne/Becker muscular dystrophy.
136. The impact of a community-wide self-care information project on self-care and medical care utilization.
137. Isolation and uses of chromosome-specific reiterated DNA.
138. Duchenne/Becker muscular dystrophy: A SHORT OVERVIEW OF THE GENE, THE PROTEIN, AND CURRENT DIAGNOSTICS.
139. Composition of peripheral blood progenitor cell components collected from healthy donors.
140. Treatment of indolent lymphoma with fludarabine/mitoxantrone combination: a phase II trial.
141. Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
142. Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts.
143. Molecular heterogeneity of translocations associated with muscular dystrophy.
144. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
145. The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies.
146. Autologous transplantation of mobilized peripheral blood CD34+ cells selected by immunomagnetic procedures in patients with multiple myeloma.
147. Rapid engraftment after allogeneic transplantation using CD34-enriched marrow cells.
148. Identification of a C6/G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus.
149. Variation in Phytopathogenic Viruses.
150. Primary g-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile
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